Indian Patents
Title of Invention

CARBOXAMIDE DERIVATIVES AS MUSCARINIC RECEPTOR ANTAGONISTS
Abstract The invention relates to compounds of Formula (I) processes and intermediates for their prepa¬ration, their use as muscarinic antagonists and pharma¬ceutical composition containing them.
Full Text Carboxamide derivatives as muscarlntc receptor antagonists
This Invention relates to compounds of general formula (I):
(Formula Removed)
in which R1, R2, R3, A, A1 and p have the meanings indicated below, and to processes and intermediates for the preparation of, compositions containing and the uses of such derivatives.
Cholinerglc muscarinic receptors are members of the G-protein coupled receptor super-family and are further divided into 5 subtypes, M1 to M5. Muscarinic receptor sub-types are widely and differentially expressed In the body. Genes have been cloned for all 5 sub-types and of these, M1, M2 and M3 receptors have been extensively pharmacologically characterized in animal and human tissue. M1 receptors are expressed in the brain (cortex and hippocampus), glands and in the ganglia of sympathetic and parasympathetlc nerves. M2 receptors are expressed in the heart, hindbrain, smooth muscle and in the synapses of the autonomic nervous system. M3 receptors are expressed in the brain, glands and smooth muscle. In the airways, stimulation of M3 receptors evokes contraction of airway smooth muscle leading to bronchoconstriction, while in the salivary gland M3 receptor stimulation increases fluid and mucus secretion leading to increased salivation. M2 receptors expressed on smooth muscle are understood to be pro-contractile while pre-synaptic M2 receptors modulate acetylcholine release from parasympathetic nerves. Stimulation of M2 receptors expressed in the heart produces bradycardia.
Short and long-acting muscarinic antagonists are used in the management of asthma and COPD; these include the short acting agents Atrovent® (ipratropium bromide) and Oxivent® (oxitropium bromide) and the long acting agent Spiriva® (tiotropium bromide). These compounds produce bronchodilation following inhaled administration. In addition to improvements in spirometric values, anti-muscarinic use in chronic obstructive pulmonary disease (COPD) is associated with improvements in health status and quality of life scores. As a consequence of the wide distribution of muscarinic receptors in the body, significant systemic exposure to muscarinic antagonists is associated with effects such as dry mouth, constipation, mydriasis, urinary retention (all predominantly mediated via blockade of M3 receptors) and tachycardia (mediated by blockade of M2 receptors). A commonly reported side-effect following inhaled administration of therapeutic dose of the current, clinically used
non-selective muscarinic antagonists is dry-mouth and while this is reported as only mild in-Intensity it does limit the dose of inhaled agent given.
Accordingly, there is still a need for improved M3 receptor antagonists that would have an appropriate pharmacological profile, for example in term of potency, pharmacokinetics or duration of action. In this context, the present invention relates to novel M3 receptor antagonists. In particular, there is a need for M3 receptor antagonists that would have a pharmacological profile suitable for an administration by the inhalation route.
The scientific literature discloses many compounds having a muscarinic receptor antagonist activity. As a matter of example, EP0948964A1 discloses compounds of formula
(Formula Removed)
in which R denotes a hydrogen atom, a halogen atom or a lower alkpxy group. The invention relates to a compound of formula (I)
(Formula Removed)
wherein,
-R1 is CN or CONH2; - A is selected from
(Formula Removed)
or wherein * and ** represent the attachment points, ** being linked to the oxygen,
- R2 and R3 are methyl, or, where A is a group of formula
(Formula Removed)
R2 and R3 may also together form with the carbon atom to which they are linked a cyclopentane ring; -p is 0 or 1;
- A1 is selected from
a) phenyl optionally substituted with 1, 2 or 3 groups independently selected from halo,.
CN, CF3, OR4, SR4, OCF3, (C1-C4)allcyl and phenyl optionally substituted with OH;
b) naphthyl optionally substituted with 1 or 2 groups independently selected from halo,
CN, CF3, OR4, SR4, OCF3 and (C1-C4)aikyl;
c) a 9 or 10-membered bicyclic aromatic heterbcycllc group, containing from 1, 2 or 3
heteroatoms independently selected from 0, S or N, said heterocycllo group being
optionally substituted with 1 or 2 substituents independently selected from OR4, (C1-
C4)alkyl and halo;
R4 is H or (C1-C4)alkyl; )r, if appropriate, the pharmaceutically acceptable salts or solvates thereof.
n the here above general formula (I), (C1-C4)alkyl denote a straight-chain or branched group :ontaining 1, 2, 3 or 4 carbon atoms. This also applies if they carry substituents or occur as substituents of other radicals, for example In 0-(C1-C4)alkyl radicals, S-(C1-C4)alkyl radicals stc.... Examples of suitable (C1-C4)alkyl radicals are methyl, ethyl, n-propyl, /so-propyl, n-butyl, so-butyl, sec-butyl, tert-butyL.. Examples of suitable 0-(C1-C4)alkyl radicals are methoxy, 3thoxy, n-propyloxy, /so-propyloxy, n-butyloxy, /so-butyloxy, sec-butyloxy and ferf-butyloxy....
Examples of 9 or 10-membered bicyclic aromatic heterocyclic group, containing from 1, 2 or 3 heteroatoms independently selected from 0, S or N are indolyl, isoindolyl, quinolyl, soquinolyl, benzofuranyl, isobenzofuranyl, benzothienyl, isobenzothlenyl, quinazolyl, quinoxalyl, phthalazinyl, benzothiazolyl, benzoxazolyl, benzlsothiazolyl, benzisoxazolyl, benzimidazolyl, indazolyl, benzotriazolyl, benzoxadiazolyl, benzisoxadiazolyl, benzothiadiazolyl and benzisothiadiazolyl.
Preferred 9 or 10-membered bicyclio aromatic heterocyclic groups are benzoxazolyl, benzothiazolyl, benzofuranyl, benzothienyl, Isoquinolyl and quinolyl. Benzoxazolyl is particularly preferred.
Halo denotes a halogen atom selected from the group consisting of fluoro, chloro, bromo and iodo. Preferred halo groups are fluoro and chloro.
In the above compounds of formula (I) and in the intermediates useful for their preparation,
the following definitions are preferred:
Preferably, R1 is CONH2.
Preferably, R4 is H or CH3.
Preferably, A1 Is phenyl optionally substituted with 1,2 or 3 groups independently selected
from F, Cl, CF3, OH, OCH3, OCF3and CH3. More preferably, A1 is phenyl optionally
substituted with 1 or 2 groups independently selected from F, Cl, CF3, OH, OCH3, OCF3and
CH3.
Preferably, A1 is naphthyl optionally substituted with OH.
Preferably, A1 is benzoxazolyl.
Preferably, R2 and R3 are methyl.
In a preferred embodiment, p is 0.
In another preferred embodiment, p is 1.
In a preferred embodiment, the compound of formula (I) wherein A Is a group of formula

(Formula Removed)
has the below (R) configuration:
(Formula Removed)
R2 R3 In a preferred embodiment, the compounds of formula (I) wherein A is a group of formula

(Formula Removed)
has the below (S) configuration:
(Formula Removed)
Preferred compounds according to the invention are:
5-Methyl-5-[(3S)-3-phenoxypyrrolidin-1-yl]-2,2-diphenylhexanenitrile;
5-Methyl-5-[(3S)-3-phenoxypyrrolidln-1-yl]-2,2-d!phenylhexanamide;
5-Methyl-5-[(3R)-3-phenoxypyrrolidin-1-yl]-2,2-diphenylhexanenitrile;
5-Methyl-5-[(3R)-3-phenoxypyrrolidin-1-yl]-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Methoxyphenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanenitriIe;
5-[{3S)-3-(3-methoxyphenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Hydroxyphenoxy)pyrrolidln-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(Benzyloxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanenitrile;
5-[(3R)-3-(Benzyloxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(Benzyloxy)pyrrol!din-1-yl]-5-methyl-2,2-diphenylhexanenitrile;
5-[(3S)-3-(Benzyloxy)pyrrolidin-i-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-Methoxyphenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3'(3-Hydroxyphenoxy)pyrrolidln-1-yl]-5-m6thyl-2,2-d!phenylhexanamide;
5-Methyl-5-[(3S)-3-(3-methylphenoxy)pyrrolidin-1-yl]-2,2-diphenylhexanamid6;
5-[(3R)-3-(1,3-Benzoxazol-6-yloxy)pyrrolidin-1-yl]-5-methy!-2,2-diphenyIhexanamide;
5-[(3S)-3-(4-Chlorophenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Bromophenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-{(3S)-3-[(3l-Hydroxyb!phenyl-4-yl)oxy]pyrrolidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-{(3S)-3-[(3'-Hydroxybiphenyl-3-yl)oxylpyrrolidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
6-{(3S)-3-[(6-Hydroxy-2-naphthyl)oxy]pyrroIidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-I(3S)-3-(2-Hydroxyphenoxy)pyrrolidln-1-yl>5-methyl-2,2-diphenylhexanamid6-,
5-[(3S)-3-(4-methoxyphenoxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(4-hydroxyplrienoxy)pyrrolidin-1-yl]-5-methyl-2l2-diphenylhexanamide;
5-[(3S)-3-(4-trifluromethyl-phenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-t(3R)-3-(4-Trifluoromethyl-phenoxy)pyrrolidin-1-yl]-5-methyl-2l2diphenylhexanenitri!e;
5-[(3R)-3-(4-trifluromethyl-phenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamlde;
5-[(3R)-3-(3-chloro-4-methoxy-phenoxy)pyrrolldln-1-yl]-5-methyl-2,2-diphenylhexanenitrile;
5-[(3R)-3-(3-chloro-4-methoxy-phenoxy)pyrrolidin-1-yl]-5-methy!-2,2-dlphenylhexanamide;
5-[(3S)"3-(3-Hydroxy-5-methyl-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(3-Hydroxy-2-methyl-phenoxy)-pyrrolidin-1-yl]-5-methy!-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(2,4-Dichloro-5-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic
acid amide;
5-[(3S)-3-(4,5-Dichloro-2-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic
acid amide;
5-[(3S)-3-(3-Chloro-5-methoxy-phenoxy)-pyrrolldin-1-yl]-5-methyl-2l2-diphenyl-hexanoic acid
amide;
5.-[(3S)-3-(3-Chloro-5-hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(4-Chloro-2-Methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyI-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(4-Chloro-2-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(2-Chloro-3-Methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-dIphenyl-hexanoic acid
amide;
5-[(3S)-3-(2-Chloro-3-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-dlphenyl-hexanoic acid
amide;
. 5-[(3S)-3-(4-Chloro-3-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,Z-dlphenyl-hexanoio acid
amide; 5-[(3S)-3-(2-Chloro-5-Hydroxy-ph6noxy)-pyrrolidin-1-yl]-5-methyl-2,2-dipheny|-hexanoic acid
amide;
5-[(3R)-3-(3-Chloro-2-Methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-dlphenyl-hexanenitrile; 5-[(3R)-3-(3-Chloro-2-Methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide; 5-t(3R)-3-(3-Chloro-2-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide; 5-[(3S)-3-(3-Hydroxy-2,5-dimethyl-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic
acid amide; 5-[(3S)-3-(3-Fluoro-5-Methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide; 5-[(3S)-3-(3-Fluoro-5-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3R)-3-(3-Methoxy-5-trifluoromethyl-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-
hexanenitrile; •
5-{(3R)-3-(3-Methoxy-5-trifluoromethyl-phenoxy)-pyiTolidin-1-yl]-5-methyl-2,2-diphenyl-
hexanoic acid amide;
5-[(3R)-3-(3-Hydroxy"5-trifluoromethyl-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-
hexanoic acid amide;
5-[(3S)-3-(4-Fluoro-3-Methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(2-Fluoro-3-Methoxy-phenoxy)-pyrrolidln-1-yl]-5-methyl-2I2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(4-Fluoro-3-Hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(2-Fluoro-3-Hydroxy-phenoxy)-pyrrolidin-1 -yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3R)-3-(3-Hydroxy-benzyloxy)-pyrrolidin-1 -yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
5-{(3S)-3-[(3-Bromobenzyl)oxy]pyrrolidin-1-yl}-5-[nethy-2,2-diphenylhexanenitrile;
5-{(3S)-3-[(3'-Hydroxybiphenyl-3-yl)methoxy]pyrrolidin-1-yl}-5-methyl-2,2-
diphenylhexanenitrile;
5-[(3S)-3-(Biphenyl-3-yImethoxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanenitrile;
5-{(3S)-3-[(2'-Hydroxybiphenyl-3-yl)methoxy]pyrrolidin-1-yl}-5-methyl-2,2-
diphenylhexanenitrile;
5-{(3S)-3-[(4-Bromobenzyl)oxy]pyrrolidin-1-yl}-5-methyl-2,2-diphenylhexanenitrile;
5-{(3S)-3-[(3'-Hydroxybiphenyl-4-yl)methoxy]pyrrolidin-1-yl}-5-methyl-2,2-
diphenylhexanenitrile;
5-{(3S)-3-t(3'-Hydroxybiphenyl-3-yl)methoxy]pyrrolidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-{(3S)-3-[(4'-Hydroxybiphenyl-3-yl)methoxy]pyrrolidin-1-yl}-5-m8thyl-2,2-dlphenylhexanenltrile;
diphenylhexanamide; '
5-{(3S)-3-[(2'-Hydroxybiphenyl-3-yl)methoxy]pyrrolldin-1-yl}-5-methyl-2l2-
diphenylhexanamide;
5-{(3S)-3-[(3l-Hydroxybiphenyl-4-yl)methoxy]pyrrolidin-1-yl}-5-methyl-2,2-
dlphenylhexanamide;
5-[(3S)-3-(Biphenyl-3-ylmethoxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(4-Fluoro-3-hydraxy-ben2yloxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Cyano-5-hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamlde;
5-t(3S)-3-(2-Cyano-5-methoxy-phenoxy)-pyrrolidin-1-y^5-methyl-2,2-diphenylhexanamide;
5-{(3S)-3-[(7-Hydroxy-2-naphthyl)oxy]pyrrolidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(4-Phenylphenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-chloro-4-hydroxyphenbxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-F!uoro-5-methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-Fluoro-5-hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenyl-hexanamide;
5-[(3R)-3-(2-Fluoro-3-methoxy-phenoxy)-pyrrolidIn-1-yl]-5-methyl-2l2-diphenylhexanamide;
5-[(3R)-3-(2-Fluoro-3-hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2l2-diphenylhexanamide;
5-[(3R)-3-(2-Chloro-3-methoxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(2-Chloro-3-hydroxy-phenoxy)-pyrrolIdin-1-yll-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(4-Chloro-3-hydroxy-benzyloxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamlde;
5-[(3R)-3-(3-methoxy-4-chloro-phenoxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanenitrile-,
5-[(3R)-3-(3-methoxy-4-ohloro-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-hydroxy-4-chloro-phenoxy)-pyrrolldin-1-yl]-5-methyl-2,2-diphenylhBxanamide;
5-[(3R)-3-(3-hydroxy-4-cyano-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-dlphenylhexanamlde;
5-[(3S)-3-(3-methoxy-benzyloxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanamlde;
5-[(3R)-3-(2-Chloro-3-hydroxy-benzyloxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-Methyl-5-(4-phenoxypiperidin-1-yl)-2,2-diphenylhexanenitrile;
5-{4-[(3-Bromobenzyl)oxy]plperidin-1-yl}-5-methyl-2,2-diphenylhexanenitrile;
5-{4-[(3-Hydroxybenzyl)oxy]plperidln-1-yl}-5-methyl-2,2-diphenylhexanenitrile;
5-[4-(BBnzyloxy)piperldin-1-yl]-5-methy!-2,2-diphenylhexanenitri!e;
5-Methyi-5-(4-phenoxypiperldin-1-yl)-2,2-diphenylhexanamide;
5-{4-[(3-Bromobenzyl)oxy]piperidin-1-yl}-5-methyI-2,2-diphenylhexanamide;
5-[4-(Benzyloxy)piperidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[4-(2,4-DIchloro-5-hydroxy-phenoxy)-pIperidin-1-yl]-5-methyl-2,2-diphenylhexanoic acid
amide;
5-[4-(4-Cyano-2,5-difluoro-phenoxy)-plperidin-1-yl]-5-methyl-2,2-diphenylhexanoic acid
amide;
5.[4-(3.hydroxyphenoxy)piperidin-1-yl]-5-methy\-2,2-diphenylhBxanamide;
5-[4-(3-hydroxy-2-methylphenoxy)piperldln-1-yl]-5-methyl-2,2-dlphenylhexanamide;
5.{4-[(3'-hydroxybiphenyl-3-yl)methoxy]piperidin-1-yl}-5-methyl-2l2-dlphenylhexanenitrile;
5.{4.[(3i.llycjroxyblphenyl-3-yl)methoxy]piperidin-1-yl}-6-methyl-2,2-dIphenylhexanamide;
5-[3-((3-Methoxyphenoxy)azetidin-1-yl]-5-methyl-2,2-diphenylhexanenitrile;
5-[3-((3-Methoxyphenoxy)azetidln-1-yl]-5-methyl-2,2-diphenylhexanamlde;
5-[3-((BenzyIoxy)az6tidin-1-yl]-5-methyl-2,2-dlph6nylhexanenitrile;
5-t3-(Benzyloxy)az6tldin-1-yl]"5-methyl-2,2-diphenylhexanamide;
5-Methyl-5-(3-phenoxyazetidin-1-yl)-2,2-dlphenylhexanenitrile;
5-Wlethyl-5-(3-phenoxyazetldln-1-yl)-2,2-diphenylhexanamide;
5-[3-((4-Methoxyph6noxy)azetldln-1-yl]-5-methyl-2,2-diphenylhexanenitrile;
5-l3-(4"Methoxyph6noxy)azetidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[3-((4-hydroxyphenoxy)azetldin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-l3-(3-Hydroxyphenoxy)azetidin-1-y)]-5-methyl-2,2-diphenylhexanamide;
5-[3-((2-Hydroxyphenoxy)azetidln-1-yl]-5-methyl"2,2-diphenylhexanamide;
5-{3-(2,4-Dichloro-5-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-dlphenylhexanamide;
5-{3-(4,5-Dichloro-2-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanamlde;
5-[3-((4-Chloro-3-methoxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanenitrile;
5-{3-(4-Chloro-3-methoxy-phenoxy)-azetldin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-{3-(4-Chloro-3-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-[3-((3-Hydroxy-benzyloxy)-azetidln-1-yl]-5-methyl-2,2-dlphenyl-hexano!c acid amide;
5-[3-((2-Chloro-5-methoxy-phenoxy)-azetldin-1-yl]-5-methyl-2,2-diphenyl-hexanenitrile;
5-[3-((2-Chloro-5-methoxy-phenoxy)-azetldln-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
5-[3-((2-Chloro-5-hydroxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
5-[3-((3-Fluoro-5-methoxy-phenoxy)-azetidin-1-yl]-5-methyI-2,2-diphenyl-hexanenitrile;
5-[3-((3-Fluoro-5-methoxy-phenoxy)-azetldln-1 -yl]-S-methyl-2,2-dlphenylhexanamide;
5-{3-(3-Fluoro-5-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2l2-diphenylhexanamide;
5-[3-((3-Chloro-5-methoxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanenitrile;
5-[3-((3-Chloro-6-methoxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-{3-(3-Chloro-5-hydroxy-phenoxy)-azetidin-1-yl}-5-methyI-2,2-diphenylhexanamide;
5-[3-((4-Fluoro-2-methoxy-phenoxy)-azetidln-1-yl]-5-methyl-2,2-diphenyl-hexanenltrile;
5-[3-((4-Fluoro-2-methoxy-phenoxy)-azetidin-1-yl]-5-methyI-2,2-diphenyIhexanamide;
5-{3-(4-Fluoro-2-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
5-[3-((2,6-Dichloro-3-hydroxy-benzyloxy)-azetidln-1-yl]-5-methyl-2,2-diphenyl-hexanolc acid
amide;
4-{1-[3-(3-Methoxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2,2-diphenyl-butyronitrlle;
4-{1-[3-(3-Methoxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2,2-dlphenyi-butyramide;
4-{1-l3-(3-Hydroxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2,2-diphenyl-butyramide;
5-[3-((2-Fluoro-3-methoxy-phenoxy)-azetidln-1-yl]-5-methyl-2,2-diphenyl-hexanenitrile;
5-[3-((2-Fluora-3-methoxy-phenoxy)-azetidln-1-yl]-5-methyl-2,2-diphenyl-hexanolc acid amide;
5-[3-((2-Fluoro-3-hydroxy-phenoxy)-azetidln-1 -yll-S-methyW^-dlphenyl-hexanolc acid amide;
5-[3-((2-Fluoro-5-methoxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanenitrlle;
5-[3-((2-Fluoro-5-methoxy-phenoxy)-azetidin-1-yl]-5-methy!-2,2-diphenyl-hexanoic acid amide;
5-[3-((2-Fluoro-5-hydroxy-phenoxy)-azetidin-1 -yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
5-t3-(4-Chloro-3-hydroxy-benzyloxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
4-{1-[3.(4-Chloro-3-hydroxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2l2-diphenyl-butyramIde; •
5-[3-((3-BroiDo-5-methoxy-phenoxy)-azetidin-1-ylI-5-methyl-2,2-diphenyl-hexanenitriIe;
5-[3-((3-Bromo-5-methoxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-dlphenyl-hexanoic acid amide;
5-[3-((3-Bromo-5-hydroxy-phenoxy)-azetidin-1-yI]-5-methyl-2,2-diphenyl-hexanoic acid amide;
4-{1-[3-(3-Fluoro-4-methoxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2,2-diphenyl-butyronitriIe;
4-{1-[3-(3-Fluoro-4-methoxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2,2-diphenyl-butyramide;
4-{1-[3-(3-Fluoro-4-hydroxy-phenoxy)-azetldin-1-yl]-cyclopentyl}-2,2-diphenyl-butyramide;
5-[3-((3-Chloro-4-hydroxy-benzyloxy)-azetidin-1-y)]-5-methyl-2,2-diphenyl-hexanoic acid
amide; ,
5-[3-((4-Chloro-2-hydroxy-benzyloxy)-azetidin-1-yl]-5-methyl-2,2-dlphenyl-hexanoic acid
amide;
5-[3-((2-Chloro-3-hydroxy-benzyloxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[3-((3,5-Dihydroxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanoicacid amide;
5-[3-((3-Hydroxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanenitrile;
5-{3-[(4-Hydroxybenzyl)oxy]azetidin-1-yl}-5-methyl-2l2-diphenylhexanenitrile; and,
5-[3-((4-Hydroxy-benzyloxy)-azetidin-1 -yl]-5-methyl-2,2-diphenyl-hexanoic acid amide.
More preferred compounds are:
5-Methyl-5-[(3S)-3-phenoxypyrrolidin-1-yl]-2,2-diphenylhexanamide;
5-Methyl-5-[(3R)-3-phenoxypyrrolidin-1-yl]-2,2-diphenylhexanamide;
5:[(3S)-3-(3-Hydroxyphenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-Hydroxyphenoxy)pyrrolldin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Fluoro-5-Hydroxy-phenoxy)-pyrrol!din-1-yl]-5-methyl-2,2-dipheny!-hexanoic acid
amide;
5-[(3S)-3-(2-Fluoro-3-Hydroxy-phenoxy)-pyrrolldin-1-yi]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3R)-3-(2-Fluoro-3-hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(2-Chloro-3-hydroxy-phenoxy)-pyrroIidin-1-yl]-5-methyl-2l2-diphenylhexanamide;
5-Methyl-5-(4-phenoxyplperidin-1-yl)-2,2-diphenylhexanamide;
S-^-fS-hydroxyphenoxyJpiperidin-l-yll-S-methyl^^-dlphenylhexanamide;
5-Methyl-5-(3-phenoxyazetidin-1-yl)-2,2-diphenylhexanamide;
5-[3-((3-Hydroxyphenoxy)azetidin-1-yl]-5-methyl-2,2-dlphenylhexanamide;
5.{3-(4.Chloro-3-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanarnide;
5-{3-(3-Fluoro-5-hydroxy"phenoxy)-a2etidin-1-yl}-5-methyl-2,2-diphenylhexanamlde;
5-{3-(3-Chloro-5-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanamlde;
4-{1 -[3-(3-Hydroxy-phenoxy)-azetldIn-1 -yl]-cyclopentyl}-2,2-diphenyl-butyramide;
5-[3-((2-Fluoro-3-hydroxy-phehoxy)-azetidin-1 -yI]-5-methyl-2,2-diphenyl-hexanoic acid amide;
5-[3-((2-Fluoro-5-hydroxy-phenoxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
and,
5-[3-((4-Chloro-3-hydroxy-benzyloxy)-azetidin-1-ylI-5-methyl-2,2-diphenyl-hexanoic acid
amide.
Most preferred compounds are:
5-[(3S)-3-(3-Hydroxyphenoxy)pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-Hydroxyphenoxy)pyrro!idin-1-yl]-5-methyl-2,2-diphenyIhexanamlde;
5-[(3R)-3-(2"Fluoro-3-hydroxy-phenoxy)-pyrrolidin-1-yl]-5-methyl-2,2-diphenylhexanamide;
5-[3-({3-Hydroxyphenoxy)azetidin-1-yI]-5-methyl-2,2-diphenylhexanamide;
5-{3-(4-Chloro-3-hydroxy-phenoxy)-azetidln-1-yl)~5-methyl-2,2-diphenylhexanamide;
5-{3-(3-Fluoro-5-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanamlde;
5-{3-(3-Chloro-5-hydroxy-phenoxy)-azetidin-1-yl}-5-methyl-2,2-diphenylhexanamide;
4-{1-[3-(3-Hydroxy-phenoxy)-azetidin-1-yl]-cyclopentyl}-2,2-diphenyl-butyramide;
5-[3-((2-Fluoro-3-hydroxy-phenoxy)-azetidin-1 -yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
5-[3-((2-Fluoro-5-hydroxy-phenoxy)-azetidin-1 -yl]-5-methyl-2,2-diphenyI-hexanoic acid amide;
and,
5-[3-((4-Chloro-3-hydroxy-benzyloxy)-azetidin-1-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide.
The invention also relates to processes for the preparation of the compounds of formula (I) as well as intermediates useful for their preparation. In particular, the invention relates to the below intermediates:
(Formula Removed)
(1) wherein A, p and A1 are as defined in compounds of formula (I);
(Formula Removed)
wherein A and R1 are as defined in compounds of formula (I); R1
(Formula Removed)
wherein R1, R2 and R3 are as defined In compounds of formula (I) and LG is a suitable leaving group such as mesylate ortosylate;
(Formula Removed)
wherein LG is a suitable leaving group such as mesylate or tosylate; and, CN
(Formula Removed)
(XVII) 10 wherein R2 and R3 are as defined in compounds of formula
(Formula Removed)
Compound of formula (I) may be prepared in a variety of ways. The routes below illustrate one such way of preparing these compounds; the skilled person will appreciate that other routes may be equally as practicable.
Compounds of formula (I) where A is
(Formula Removed)
may be prepared according to the routes disclosed below:
(Formula Removed)
Scheme 1
(Scheme Removed)
Wherein A is ' or
A1 and p are as defined above for the compounds of formula (I), and,
PG is a suitable carboxyl-protecting group such as methyl or tert-buty! and is typically tert-
butyl.
Compound of formula (II) is commercially available.
Compounds of formula (III) are either commercially'available or their preparation is known
from the literature.
Compounds of formula (IV) may be prepared from compounds of formula (II) and (III) by process step (i): compound (II) Is treated with compound (III) in the presence of a suitable base such as potassium hydroxide or sodium hydroxide, in a suitable solvent such as methanol, ethanol or tert-butanol, at a temperature between 25°C and elevated temperature for 6-24 hours. Typical conditions comprise of 1.0 equivalent of compound (II), 0.05eq of potassium hydroxide and 1.0 equivalent of compound (III) In tert-butanol at a temperature between 25-60°C for up to 24 hours.
Compounds of formula (V) may be prepared from compounds of formula (IV) by process step (ii). De-protection of compound (IV) may be achieved using standard methodology as described in "Protecting Groups in Organic Synthesis" by T.W. Greene and P. Wutz. When ,PG is tert butyl, typical conditions comprise of 1.0 equivalent of compound (IV) In the presence of hydrochloric acid (4M in dioxan), in dichloromethane, at room temperature for up to 18 hours. Compound of formula (VI) may be prepared as described in scheme 2:
(Scheme Removed)
Scheme 2
Compounds of formula (Via) are either commercially available or can be prepared as described In scheme 2a
(Scheme Removed)
Scheme 2a
wherein A1 and p are as defined -above for the compounds of formula (I). In some cases, A1
may be protected with a suitable protecting group. For example, when A1 contains a phenol, it
may be protected by a suitable hydroxyl protecting group..
PG1 is a suitable amlno protecting group such as tertbutoxycarbonyl (BOC),
benzyloxycarbonyl (CBz) and is typically BOC.
X Is a suitable functional group such as hydroxy, fluoro, bromo, chloro, iodo, O-mesylate or O-
tosylate and is typically hydroxy or bromo.
When PG' is BOC, compounds of formula (VIII) and (Villa) are commercially available.
Compounds of general formula (IX) are either commercially available, known in the literature,
or may be prepared as Illustrated in schemes 3-5.
(Scheme Removed)
Scheme 3
wherein A1 is as defined above for the compounds of formula (I) or may be optionally protected.
Compounds of formula (IX) where A1 is as defined for compounds of formula (I), p is 0 and X is OH, may be prepared from compounds of formula (XI) by Baeyer-Villlger oxidation and subsequent hydrolysis (process step (viii)). Typical conditions comprise reaction of 1.0 equivalent of compound (XI) with 3.0 equivalents of 3-chIoroperoxybenzoic acid, in a suitable solvent such as dichloromethane, at room temperature for 18 hours, and subsequent treatment of this product with a suitable base such as trlethylamine, In a suitable solvent such as methanol, at room temperature for 18hrs.
(Scheme Removed)
Scheme 4
Compounds of formula (IX) where A1 contains a suitably protected phenol, p is 0 and X is OH may. be prepared from compounds of formula (IXa) where A1 contains a phenol, p is 0 and X Is OH, by addition of a suitable phenol protecting group such as benzyl, by process step (ix). Typical conditions comprise reaction of 1.0 equivalent of compound (IXa) with 1.0 equivalent of benzyl bromide and 1.0 equivalent of a suitable base such as caesium carbonate, in a suitable solvent such as dimethylformamide, at 80°C for 30 minutes. Alternatively, compounds of formula (IX) where A1 contains a suitably protected phenol, p is 0 and X is OH may be prepared from compounds of formula (IXa) where A1 contains a suitably protected phenol, p is 0 and X is OMe, by mono-deprotection using conditions described in "Protecting Groups in Organic Synthesis" by T. W. Greene and P. Wutz. Compounds of formula (IX) where A1 contains a suitably protected phenol, p is 0 and X is F, may be prepared from compounds of formula (IXa) where A1 contains a phenol, p Is 0 and X is F, by addition of a suitable phenol protecting group such as methyl, by process step (ix). Typical conditions comprise reaction of 1.0 equivalent of compound (IXa) with 2.0 equivalents of methyl iodide and 1.0 equivalent of a suitable base such as potassium carbonate, in a suitable solvent such as tetrahydrofuran, at room temperature for 3 hours.
(Scheme Removed)
Scheme 5
wherein A1 is as defined above for the compounds of formula (I) or may be optionally protected.
Compounds of formula (IXa) where p is 1 and X Is OH may be prepared from compounds of formula (XI) by reduction of the aldehyde with a suitable reducing agent such as sodium borohydride, by process step (xl). Typical conditions comprise reaction of 1.0 equivalent of compound (XI) with 1.0 equivalent of sodium borohydride, in a suitable solvent such as ethanol, at room temperature for 18 hours.
Compounds of formula (XIV) where R6 represents a suitable acid protecting group such as methyl, ethyl or allyl may be prepared from compounds of formula (XIII) by addition of a suitable protecting group such as allyl, by process step (x). Typical conditions comprise reaction of 1.0 equivalent of compound (XIII) with 2.0 equivalents of allyl bromide and 2.0 equivalents of a suitable base such as potassium carbonate, in a, suitable solvent such as dimethylformamlde, at room temperature for 18 hours.
Compounds of formula (IXa) where p is 1 and X is OH may be prepared from compounds of formula (XIV) by reduction of the ester with a suitable reducing agent such as lithium aluminium hydride, by process step (xi). Typical conditions comprise reaction of 1.0 equivalent of compound (XIV) with 2.0 equivalent of lithium aluminium hydride, in a suitable solvent such as tetrahydrofuran, at 0°C to room temperature over 5 hours. Compounds of formula (IX) where p is 1 and X is halo may be prepared from compounds of formula (IXa) where p is 1 and X is OH, by halogenation of the primary alcohol using a suitable reagent such as thionyl chloride, dibromotriphenylphosphqrane or iodine plus
triphenyl phosphine, preferably thionyl chloride or dibromotriphenylphosphorane, in a suitable
r solvent such as dichloromethane or acetonitrile, by process step (xii). When X is bromo,
Typical conditions comprise reaction of 1.0 equivalent of compound (IXa) with 1.0 equivalent of dibromotriphenylphosphorane, In a suitable solvent such as acetonitrile, at room temperature for 18 hours. When X is chloro, Typical conditions comprise reaction of 1.0 equivalent of compound (IXa) with 2.5 equivalent of thionyl chloride in dichloromethane at room temperature for 10 minutes.
Compounds of formula (X) where p is 0 may be prepared from compounds of formulae (VIII), and (IX) where X is OH and p is 0, by a Mitsunobu reaction, between compounds (VIII) and (IX) in the presence of a suitable phosphine such as tri- "butyl phosphine or triphenyl phosphine and a suitable azo compound such as diethylazodicarboxylate, diisopropylazodicarboxylate or di-tert-butylazodlcarboxylate, in a solvent such as dichloromethane, tetrahydrofuran or N.N-dimethylformamlde, at temperatures between 25-115°C, for 1-48 hours, by process step (vi). Typical conditions comprise of 1.0 equivalent of compound (VIII), 1.0 equivalent of compound (IX) 1.0-1.2 equivalents of triphenylphosphine and 1.0-1.2 equivalents of di-lsopropylazodlcarboxylate, in tetrahydrofuran, at 25°C for up to 18 hours. Compounds of formula (Xa) where p is 0 may be prepared from compounds of formula (Villa) and (IX) using the same conditions.
Compounds of formula (X) where p is 1 may be prepared from compounds of formulae (VIII), and (IX) where X Is halo and p is 1, by treatment of compound (VIII) with a suitable strong base such sodium hydride or potassium tert-butoxide followed by quench with compound (IX), In a suitable solvent such as tetrahydrofuran or dimethyl formamide, at a temperature between 0°C and room temperature, for 1-18 hours, by process step (vi). Typical conditions comprise of 1.0 equivalent of compound (VIII), 1.0 equivalent of sodium hydride and 1.0 equivalent of compound (IX), In tetrahydrofuran, at temperatures between 0-25°C for up to 18 hours. Compounds of formula (Xa) where p is 1 may be prepared from compounds of formula (Villa) and (IX) using the same conditions.
Compounds of formula (VI) may be prepared from compounds of formula (X) by process step (vii). De-protection of compound (X) may be achieved using standard methodology as described in "Protecting Groups in Organic Synthesis" by T.W. Greene and P. Wutz. When PG1 is BOG, typical conditions comprise of 1.0 equivalent of compound (X) in the presence of hydrochloric acid (4M in dioxan), in dichloromethane, at room temperature for up to 18 hours. Compounds of formula (Via) may be prepared from compounds of formula (Xa) and using the same conditions.
Compounds of formula (VII) may be prepared from compounds of formulae (V) and (VI) or (Via) by process step (ill), coupling of (V) and (VI) or (Via) in the presence of a suitable coupling agent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, N,N'-carbonyldiimidazole, N,N'-dicyclohexylcarbodiimide, optionally in the presence of a catalyst such as 1-hydroxybenzotriazole hydrate or 1-hydroxy-7-azabenzotriazole, and optionally in the presence of a tertiary amine base such as N-methylmorpholine, triethylamine or N,N-diisopropylethylamine, In a suitable solvent such as N,N-dimethylformamide, tetrahydrofuran or dimethylsulfoxide, under ambient conditions for 1-48 hours. Typical conditions, comprise of 1.0 equivalent of compound (V), 1.0 equivalent of compound (VI) or (Via) and 1.0-1.2 equivalents of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 1.0-1.2 equivalents of 1-hydroxybenzotriazole hydrate and 1.0-1.2 equivalents trlethylafnine in dichloromethane, at room temperature for 18 hours.
Compounds of formula (la) may be prepared from compounds of formula (VII) by process step (iv). Compound (la) may be prepared in analogy to the methods of Denton and Wood (Synlett, 1999, 1, 55); Compound (VII) Is typically pre-activated with a suitable Lewis acid such as titanium chloride or zirconium chloride then treated with an excess of a suitable organometallic reagent such as MeMgCI or MeMgBr, in a suitable solvent such as tetrahydrofuran or diethyl ether, at a temperature between -78°C to 25°C, for 1-18 hours. Typical conditions comprise of 1.0 equivalent of compound (VII), 2 equivalents of zirconium chloride and 9.0 equivalents of MeMgCI in tetrahydrofuran, at-30°C for 4-8 hours. Compounds of formula (Ib) may be prepared from compounds of formula (la) by hydrolysis of compound (la) with an excess of potassium hydroxide in 3-'methyl-3-pentanol, at elevated temperature for up to 24 hours (process step (v)). Typical conditions comprise of 1.0
equivalent of compound (la) and 20 equivalents of potassium hydroxide in 3-methyl-3-pentanol at elevated temperature for up to 24 hours.
In a further embodiment, when p Is 1, compounds of formula (I) can be further functionalised to provide compounds of formula (Ic), as described in scheme 6
(Scheme Removed)
wherein A is or , and,
Rz and R3 are methyl.
Compounds of formula (XV) may be prepared from compounds of formula (I) where p is 1, by process step (xiii). When R1 is CN, cleavage of the benzyl ether group is typically achieved by treatment of compound (I) with an excess of iron (III) chloride, in a suitable solvent such as dichloromethane, under ambient conditions for 1-8 hours to provide compounds of formula (XV). When R1 is CONH2 treatment of compound (I) with hydrogen gas, in the presence of a suitable hydrogenation catalyst such as 20% Pd(OH)2 or 10% Pd/C, optionally in the presence of a suitable acid such as hydrochloric acid, in a suitable solvent such as methanol, ethanol or tetrahydrofuran, at elevated temperature for 1-18 hours, provides compounds of formula (XV).
Compounds of formula (Ic) where p is 0 may be prepared from compounds of formula (XV) and compounds of formula (IX) where p is 0 and X is OH by process step (xiv) - using the conditions disclosed for step (vi).
Compounds of formula (Ic) where p is 0 may be prepared from compounds of formula (XV) and a compound of formula (IX) where p is 0 and X is F, by process step (xiv)- treatment of compound (XV) with a suitable strong base such sodium hydride or potassium tert-butoxide followed by quench with compound (IX), in a suitable solvent such as tetrahydrofuran or N,N-dimethylformamide, at a temperature between 0°C and elevated temperature, for 1-96 hours. Typical conditions comprise of 1.0 equivalent of compound (XV), 1.0 to 2.0 equivalents of sodium hydride and 1.0 equivalent of compound (IX), in N,N-dlmethylformamide, at temperatures between 0-60°C for 18-96hours.
Compounds of formula (Ic) where p is 1 may be prepared from compounds of formula (XV) and a compound of formula (IX) where p is 1 and X Is Cl, Br, I, O-mesylate or O-tosylate by process step (xiv), treatment- of compound (XV) with a suitable strong base such sodium hydride or potassium tert-butoxide followed by quench with compound (IX), in a suitable solvent such as tetrahydrofuran or N.N-dimethylformamide, at a temperature between 0°C and elevated temperature, for 1-96 hours. Typical conditions comprise of 1.0 equivalent of
compound (XV), 1.0 to 2.0 equivalents of sodium hydride and 1.0 equivalent of compound (IX), in N.N-dimethylformamide, at temperatures between 0-60°C for 18-96hours.
In a further embodiment, compounds of formula (I) can be further functionalised to provide compounds of formula (Id), as described In scheme 7:
(Scheme Removed)
Scheme 7
(Scheme Removed)
wherein A is " or Compounds of formula (Id) where A1 represents phenyl substituted with phenyl optionally substituted with OH, may be prepared from compounds of formula (I) where A1 is phenyl substituted with Cl, Br or I, , by process step (xv), Suzuki coupling reaction with compound (XXX) in a suitable solvent, such as 1,4-dioxane or tetrahydrofuran, in the presence of water, a suitable base such as sodium carbonate or caesium carbonate, and a palladium catalyst such as [1,1'-bis(diphenylphosphino)ferrocene]palladium (II) chloride or tetrakis(triphenyl phosphine)palladium(O). Suzuki coupling reactions can be carried out as described in the literature: Suzuki, A. Pure & Appl. Chem. 1985, 57, 1749 and references contained within; Angew. Chem. Int. Ed. 2002, 41, 4176 and references contained within. Typical conditions comprise 1.0 equivalent of compound (I), 2.0 equivalents of compound (XXX), 2.0 equivalents of sodium carbonate and 0.05 equivalents of palladium catalyst in tetrahydrofuran and water, at elevated temperature for up to 16 hours.
Compound (XVI) is either commercially available or may be prepared by methods described in the literature.
Compounds of formula (Ic) and (Id) where R1 Is CONHz may also be prepared from compounds of formula (Ic) and (Id) where R1 is CN, by hydrolysis with an excess of potassium hydroxide in 3-methyl-3-pentanol, at elevated temperature for up to 24 hours. Typlca[ conditions comprise of 1.0 equivalent of compound (Ic) or (Id) where R1 Is CN and 20 equivalents of potassium hydroxide in 3-methyl-3-pentanol at reflux for up to 24 hours.
Compounds of formula (I) where A is
may be prepared according to the routes disclosed below:
(Scheme Removed)
Schemed
wherein LG represents a suitable leaving group such as mesylate or tosylate and is preferably mesylate.
Compounds of formula (XVI) may be prepared as described in WO2003037327, page 83. PG'" represents a protecting group such as tert-butoxycarbonyl or benzyloxycarbonyl and is preferably tert-butoxycarbonyl. Alternatively, compounds of formula (XVI) may be prepared according to the following process:

(Scheme Removed)
Compounds of formula (XVIc) are commercially available or known in the literature. Compounds of formula (XVIb) may be prepared from compounds of formula (XVIc) by reaction of compounds (XVIc) with chlorosulfonyl Isocyanate, formic acid and pyridine, in a suitable solvent such as dichloromethane, at low temperature for 2 hours (process step (xxi)). Typical conditions comprise 1.0 equivalent of compound (XVIc), 1.5 equivalents of chlorosulfonyl isocyanate, 1.5 equivalents of formic acid and 1.5 equivalents of pyridine in dlchloromethane, at low temperature for 2 hours.
Compounds of formula (XVIa) may be prepared from compounds of formula (XVIb) by reaction of compounds (XVIb) with magnesium oxide, iodobenzene diacetate and rhodium acetate dimer In a suitable solvent such as dlchloromethane at room temperature for up to 24 hours (process step (xxii)). Typical conditions comprise reaction of 1.0 equivalent of compound (XVIb), 2.3 equivalent of magnesium dioxide, 1.1 equivalent of iodobenzene diacetate and 0.02 equivalent of rhodium acetate dimer in dichloromethane at room temperature for 18 hours.
Compounds of formula (XVI) may be prepared from compounds of formula (XVIa) by incorporation of a suitable protecting group such as tert-butoxycarbonyl or benzyloxycarbonyl, preferably tert-butoxycarbonyl, using conditions described in "Protecting Groups in Organic Synthesis" by T. W. Greene and P.'Wutz. Typical conditions comprise reaction of 1.0 equivalent of compound (XVIa), 1.2 equivalents of di-tert-butyl dicarbonate, 2.0 equivalents of trlethylamine and 0.2 equivalents of 4'dimethylaminopyridlne in dlchloromethane, at room temperature for 3 hours.
Compounds of formula (XVII) may be prepared from compounds of formula (II) and compounds of formula (XVI) by process step (xvi)-
1) Reaction of compounds (II) and (XVI) in the presence of a strong base such as
potassium tert butoxide or sodium hydride, in a suitable solvent such as N,N-
dimethylformamide or dimethylsulfoxide, under ambient conditions or at elevated
temperature for up to 18 hours.
2) Removal of the protecting group (when used) using suitable conditions such as 4N
hydrochloric acid in dioxan or trifluoroacetic acid or hydrogehation in the presence of
catalytic palladium, as described in "Protecting Groups in Organic Synthesis" by T.W.
Greene and P. Wutz.
Typical conditions comprise of 1.2 equivalents of compound (II), 1.0 equivalent of compound (XVI) and 1.2 equivalents of potassium tert butoxide in N,N-dimethylformamide, under
ambient conditions for up to 18 hours, followed by treatment with 4N hydrochloric acid in dloxane.
Compounds of formula (XVIII) are commercially available.
Compounds of formula (XIX) may be prepared from compounds of formula (XVII) and (XVIII) by process step (xvii)- heterocycle formation can be achieved by nucleophilic addition of compound (XVIII) by compound (XVII) followed by in situ ring closure, in a suitable solvent such as methanol or ethanol, at elevated temperature for up to 48 hours. Typical conditions comprise of 1.0 equivalent of compound (XVII) and 1.1 equivalents of compound (XVIII) in methanol, at elevated temperature for up to 48 hours.
Compounds of formula (XX) may be prepared from compounds of formula (XIX) by process step (xviii)- introduction of a suitable leaving group (LG), such as mesylate or tosylate groups by reaction of compound (XIX) with mesyl chloride/anhydride or tosyl chloride, In the presence of a suitable base such as HQnig's base, triethylamine or pyridlne, optionally in a suitable solvent such as dichloromethane or dlethyl ether, at low temperature for 1-2 hours. Typical conditions comprise of 1.0 equivalent of compound (XIX) and 3 equivalents of mesyl chloride in pyridine at low temperature for up to 1-2 hours.
Compounds of general formula (XXI) are either commercially available or are known In the literature. Compounds of formula (XXI) containing a phenol group may be protected by addition of a suitable phenol protecting group such as allyl. Typical conditions comprise reaction of 1.0 equivalent of compound (XXI) containing a phenol with 1.0 equivalent of allyl bromide and 1.0 equivalent of a suitable base such as potassium carbonate, in a suitable solvent such as dlmethylformamide, at room temperature for 18 hours. Alternatively, compounds of formula (XXI) may be prepared by mono-deprotection of a bis-protected phenol using conditions described In "Protecting Groups in Organic Synthesis" by T. W. Greene and P. Wutz.
Compounds of formula (le) can be prepared from compounds of general formula (XX) and (XXI) by treatment of compound (XXI) with a suitable base such caesium carbonate or sodium carbonate followed by quench with compound (XX), In a suitable solvent such as N,N-dimethylformamide or dimethylsulfoxide, at elevated temperature for up to 18 hours (process step (xix)). Typical conditions comprise of 1.0 equivalent of compound (XX), 3.0 equivalents of caesium carbonate and 3.0 equivalent of compound (XXI), in N,N-dimethylformamlde, at elevated temperature for up to 18 hours.
In a further embodiment, compounds of formula. (If) may be prepared from compounds of formula (le) by hydrolysis of compound (le) with an excess of potassium hydroxide in 3-
methyl-3-pentanol, at elevated temperature for up to 24 hours (process step (xx)). Typical conditions comprise of 1.0 equivalent of compound (le) and 20 equivalents of potassium hydroxide in 3-methyl-3-pentanol at elevated temperature for up to 24 hours.
Alternatively compounds of formula (I) where A Is
(Formula Removed)
and R2 and R3 are methyl may be prepared as described in scheme 9.
(Scheme Removed)
Scheme 9
wherein LG represents a suitable leaving group such as mesylate or tosylate and is preferably mesylate.
Compounds of general formula (V) may be prepared as described in W097/24325. Compounds of formula (XXII) may be prepared from compounds of general formula (V) by process step (xxiv): carboxylic acid (V) may be treated with a suitable chlorinating agent such as thlonyl chloride or oxalyl chloride, in' a suitable solvent such as N,N-dimethylformamide, acetonitrile or dichloromethane, under ambient conditions for up to 8 hours. Typical conditions comprise of 1.0 equivalent of compound (V) and 2 equivalents of oxalyl chloride in N,N-dimethylformamide, at room temperature for 2 hours.
Compounds of formula (XXIII) may be prepared as described in J. Org. Chem. 1991, 56,
6729-30.
Compounds of general formula (XXIV) may be prepared from compounds of general formula
(XXII) and (XXIII) by process step (xxv): compound (XXII) undergoes nucleophilic substitution
with compound (XXIII), in the presence of a tertiary amine base such as N-methylmorpholine,
triethylamine or N,N-diisopropylethylamine, in a suitable solvent such as N,N-
dlmethylformamide, tetrahydrofuran or dichloromethane, at low temperature for 1-8 hours.
Typical conditions comprise of 1 equivalent of compound (XXII), 1 equivalent of compound
(XXIII) and 3 equivalents of triethylamine in dichloromethane, at low temperature for 1 hour.
Compounds of general formula (XXV) may be prepared from compounds of general formulae
(XXIV) and (XXI) by process step (xxvi) using the conditions described for step (xix) in
scheme 8.
Compounds of formula (le) may be prepared from compounds of formula (XXV) using the
conditions disclosed for step (iv) of scheme 1.
Compounds of formula (If) may be prepared from compounds of formula (le) using the
conditions disclosed for step (xx) of scheme 8.
Alternatively, compounds of formula (I) may be prepared as disclosed in scheme 1, using an
intermediate of formula (Vlb)
(Formula Removed)
which is commercially available or known in the literature.
Typical conditions for step (iii) comprise of 1.0 equivalent of compound (V), 1.2 equivalent of compound (Vlb), 1.0-1.2 equivalents of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 1.0-1.2 equivalents of 1-hydroxybenzotriazole hydrate and 2.5 equivalents of N,N-diisopropylethylamlne in dichloromethane, at room temperature for 18 hours.
Alternatively, a compound of formula (le) wherein p is 1 may be prepared as described in scheme 10:



(Scheme Removed)
Scheme 10
wherein p is 1 and Hal represents halo and is typically chloro or bramo, preferably chloro. Compound of formula (XXVI) may be prepared as disclosed in scheme 5.
Compounds of general formula (le) may be prepared from compounds of general formulae (XIX) and (XXVI) by treatment of compound (XIX) with a suitable strong base such sodium hydride or potassium tert-butoxide followed by quench with compound (XXVI), In a suitable solvent such as tetrahydrofuran, at a temperature between 0°C and room temperature, for 1-8 hours. Typical conditions comprise of 1.0 equivalent of compound (XIX), 1.2 equivalents of sodium hydride and 1.5 equivalents of compound (XXVI), in tetrahydrofuran, at temperatures between 0-25°C for up to 1-2 hours.
Alternatively, compounds of formula (If) may be prepared as described in scheme 11. (Scheme Removed)
Scheme 11
wherein Hal represents halo and is typically chloro or bromo, preferably chloro.
Compounds of formula (XXVII) are prepared from compounds of formula (If), where A1
represents phenyl and p=1, by removal of the benzyl group using standard hydrogenation
conditions as described in "Protecting Groups in Organic Synthesis" by T. W. Greene and P.
Wute.
Compounds of formula (If) are prepared from compounds of formula (XXVII) and compounds
of formula (XXVI), using the conditions disclosed in step (xxix).
Alternatively, compounds of formula (If) may be prepared as described In scheme 12.
(Scheme Removed)
Scheme 12
wherein LG represents a suitable leaving group such as mesylate or tosylate and is preferably
mesylate.
Compounds of formula (XXVIII) can be prepared from compounds of formula (XXVII) by
process step (xviii), as described in scheme 8.
Compounds of formula (If) can be prepared from compounds of formula (XXVIII) and
compounds of formula (XXI) by process step (xix), as described in scheme 8.
When A1 contains a suitably protected phenol, compounds of formula (I) are deprotected to
provide the corresponding phenol. Suitable protecting groups (PG") include methyl, benzyl,
allyl and tert-butyldimethylsilyl (TBDMS). De-protection may be achieved using standard
methodology as described in "Protecting Groups in Organic Synthesis" by T.W. Greene and
'P.Wutz.
When PG" Is methyl, Typical conditions of this procedure comprise of 1.0 equivalent of
protected compound of formula (I) and 1-4 equivalents of 1M boron tribromide in
dichloromethane, in a suitable solvent such as dichloromethane, at ambient temperature for
1-18 hours.
When PG" is allyl, Typical conditions of this procedure comprise of 1.0 equivalent of protected
compound of formula (I) and 20 equivalents of potassium hydroxide in 3-methyl-3-pentanol at
reflux for 1-24hrs, followed by isolation of the residue and treatment with hydrochloric acid
(4M in dioxan), in water, at 60°C for 20mins. Alternative conditions of this procedure comprise
of 1.0 equivalent of protected compound of formula (I), 6 equivalents of sodium borohydride
and 0.1 equivalents of tetrakis(triphenylphosphine)palladium(0) in tetrahydrofuran at elevated
temperature for 30 minutes.
When PG" is TBDMS, Typical conditions of this procedure comprise of 1.0 equivalent of
protected compound of formula (I) and 10 equivalents of ammonium fluoride in methanol and
water at 50 °C for 18-24hrs.
Pharmaceutically acceptable salts of the compounds of formula (I) include the acid addition and base salts thereof.
Suitable acid addition salts are formed from acids which form non-toxic salts. Examples include the acetate, adipate, aspartate, benzoate, besylate, bicarbonate/carbonate, bisulphate/sulphate, borate, camsylate, citrate, cyclamate, edisylate, esylate, formate, fumarate, gluceptate, gluconate, glucuronate, hexafluorophosphate, hibenzate, hydrochloride/chloride, hydrobromlde/bromide, hydrolodide/iodide, isethionate, lactate, malate, maleate, malonate, mesylate, methylsulphate, naphthylate, 2-napsylate, nicotinate, nitrate, orotate, oxalate, palmitate, pamoate, phosphate/hydrogen phosphate/dihydrogen phosphate, pyroglutamate, saccharate, stearate, succinate, tannate, tartrate, tosylate, trlfluoroacetate and xinofoate salts.
Suitable base salts are formed from bases which form non-toxic salts. Examples include the aluminium, arginine, benzathine, calcium, choline, diethyiamine, diolamine, glycine, lysine, magnesium, meglumine, olamine, potassium, sodium, tromethamine and zinc salts.
Hemlsalts of acids and bases may also be formed, for example, hemisulphate and hemicalcium salts.
For a review on suitable salts, see Handbook of Pharmaceutical Salts: Properties. Selection and Use by Stahl and Wermuth (Wiley-VCH, 2002).
Pharmaceutically acceptable salts of compounds of formula (I) may be prepared by one or
more of three methods:
(i) by reacting the compound of formula (I) with the desired acid or base;
(ii) by removing an acid- or base-labile protecting group from a suitable precursor of the
compound of formula (I) or by ring-opening a suitable cyclic precursor, for example, a
lactone or lactam, using the desired acid or base; or (Hi) by converting one salt of the compound of formula (I) to another by reaction with an
appropriate acid or base or by means of a suitable ion exchange column. All three reactions are typically carried out in solution. The resulting salt may precipitate out and be collected by filtration or may be recovered by evaporation of the solvent. The degree of ionisatlon in the resulting salt may vary from completely ionised to almost non-ionised.
The compounds of the invention may exist in a continuum of solid states ranging from fully amorphous to fully crystalline. The term 'amorphous' refers to a state in which the material lacks long range order at the molecular level and, depending upon temperature, may exhibit the physical properties of a solid or a liquid. Typically such materials do not give distinctive X-ray diffraction patterns and, while exhibiting the properties of a solid, are more formally described as a liquid. Upon heating, a change from solid to liquid properties occurs which is characterised by a change of state, typically second order ('glass transition'). The term 'crystalline1 refers to a solid phase in which the material has a regular ordered internal structure at the molecular level and gives a distinctive X-ray diffraction pattern with defined peaks. Such materials when heated sufficiently will also exhibit the properties of a liquid, but the change from solid to liquid is characterised by a phase change, typically first order ('melting .point').
The compounds of the invention may also exist in unsolvated and solvated forms. The term 'solvate' is used herein to describe a molecular complex comprising the compound of the invention and one or more pharmaceutically acceptable solvent molecules, for example, ethanpl. The term 'hydrate' is employed when said solvent is water,
A currently accepted classification system for organic hydrates is one that defines isolated site, channel, or metal-ion coordinated hydrates - see Polymorphism In Pharmaceutical Solids by K. R. Morris (Ed. H. G. Brittain, Marcel Dekker, 1995). Isolated site hydrates are ones in which the water molecules are isolated from direct contact with each other by intervening organic molecules. In channel hydrates, the water molecules lie in lattice channels where they are next to other water molecules. In metal-Ion coordinated hydrates, the water molecules are bonded to the metal ion.
When the solvent or water is tightly bound, the complex will have a well-defined stoichlometry independent of humidity. When, however, the solvent or water is weakly bound, as in channel solvates and hygroscopic compounds, the water/solvent content will be dependent on humidity and drying conditions. In such cases, non-stoichiometry will be the norm.
Also included within the scope of the Invention are multi-component complexes (other than salts and solvates) wherein the drug and at least one other component are present in stoichiometric or non-stoichiometric amounts. Complexes of this type include clathrates (drug-host inclusion complexes) and co-crystals. The latter are typically defined as crystalline complexes of neutral molecular constituents which are bound together through non-covalent interactions, but could also be a complex of a neutral molecule with a salt. Co-crystals may be prepared by melt crystallisation, by recrystallisation from solvents, or by physically grinding the components together - see Chem Commun, 17., 1889-1896, by O. Almarsson and M. J. Zaworotko (2004). For a general review of multi-component complexes, see J Pharm Sci, 61 (8), 1269-1288, by Haleblian (August 1975).
The compounds of the invention may also exist in a mesomorphic state (mesophase or liquid crystal) when subjected to suitable conditions. The mesomorphic state Is intermediate between the true crystalline state and the true liquid state (either melt or solution). Mesomorphism arising as the result of a change in temperature is described as 'thermotropic' and that resulting from the addition of a second component, such as water or another solvent, is described as 'lyotropic'. Compounds that have the potential to form lyotropic mesophases are described as 'amphiphilic' and consist of molecules which possess an ionic (such as -COO'Na*, -COO'K*. or -SO3'Na*) or non-ionic (such as -N'N+(CH3)3) polar head group. For more Information, see Crystals and the Polarizing Microscope by N. H. Hartshorne and A. Stuart, 4th Edition (Edward Arnold, 1970).
Hereinafter all references to compounds of formula (I) include references to salts, solvates, multi-component complexes and liquid crystals thereof and to solvates, multi-component complexes and liquid crystals of salts thereof.
The compounds of the invention include compounds of formula (I) as hereinbefore defined, including all polymorphs and crystal habits thereof, prodrugs and isomers thereof (including optical, geometric and tautomeric isomers) as hereinafter defined and isotopically-labeled compounds of formula (I).
As indicated, so-called 'prodrugs' of the compounds of formula (1) are also within the scope of the invention. Thus certain derivatives of compounds of formula (I) which may have little or no pharmacological activity themselves can, when administered into or onto the body, be
converted into compounds of formula (I) having the desired activity, for example, by hydrolytic cleavage. Such derivatives are referred to as 'prodrugs'. Further information on the use of prodrugs may be found in Pro-drugs as Novel Delivery Systems. Vol. 14, ACS Symposium Series (T. Higuchl and W. Stella) and Bloreversible Carriers in Drug Design. Pergamon Press, 1987 (Ed. E. B. Roche, American Pharmaceutical Association).
Prodrugs in accordance with the invention can, for example, be produced by replacing appropriate functionalities present In the compounds of formula (I) with certain moieties known to those skilled in the art as 'pro-moieties' as described, for example, in Design of Prodrugs by H. Bundgaard (Elsevier, 1985).
Some examples of prodrugs in accordance with the invention include
(i) where the compound of formula (I) contains a carboxylic acid functionality
(-COOH), an ester thereof, for example, a compound wherein the hydrogen of the carboxylic acid functionality of the compound of formula.(I) is replaced by (Cr C8)alkyl;
(ii) where the compound of formula (I) contains an alcohol functionality (-OH), an ether thereof, for example, a compound wherein the hydrogen of the alcohol functionality of the compound of formula (I) is replaced by (CVCeJalkanoyloxymethyl; and
(Hi) where the compound of formula (I) contains a primary or secondary amino functionality (-NH2or-NHR where R # H), an amide thereof, for example, a compound wherein, as the case may be, one or both hydrogens of the amino functionality of the compound of formula (I) is/are replaced by (CrC10)alkanoyl.
Further examples of replacement groups in accordance with the foregoing examples and examples of other prodrug types may be found in the aforementioned references.
Moreover, certain compounds of formula (I) may themselves act as prodrugs of other compounds of formula I.
Also included within the scope of the invention are metabolites of compounds of formula I, that is, compounds formed in vivo upon administration of the drug. Some examples of metabolites in accordance with the invention include (i) where the compound of formula (I) contains a methyl group, an hydroxymethyl
derivative thereof {-CH3 -> -CH2OH): .(ii) where the compound of formula (I) contains an alkoxy group, an hydroxy derivative
thereof (-OR->-OH); (iii) where the compound of formula (I) contains a tertiary amino group, a secondary
amino derivative thereof (-NR1R2 -> -NHR1 or -NHR2);
(iv> where the compound of formula (I) contains a secondary amino group, a primary
derivative thereof (-NHR1 -> -NH2); (v) where the compound of formula (I) contains a phenyl moiety, a phenol derivative
thereof (-Ph -> -PhOH); and (vl) where the compound of formula (I) contains an amide group, a carboxylic acid
derivative thereof (-CONH2 -> COOH).
Compounds of formula (I) containing one or more asymmetric carbon atoms can exist as two or more stereoisomers. Where a compound of formula (I) contains an alkenyl or alkenylene group, geometric cisltrans (or Z/E) isomers are possible. Where structural isomers are interconvertible via a low energy barrier, tautomeric Isomerism ('tautomerism') can occur. This can take the form of proton tautomerism in compounds of formula (I) containing, for example, an imino, keto, or oxime group, or so-called valence tautomerism in compounds which contain an aromatic moiety. It follows that a single compound may exhibit more than one type of isomerism.
Included within'the scope of the present invention are all stereoisomers, geometric isomers and tautomeric forms of the compounds of formula I, Including compounds exhibiting more than one type of isomerism, and mixtures of one or more thereof. Also included are acid addition or base salts wherein the counterlon is optically active, for example, of-lactate or /-lysine, or racemic, for example, rfMartrate or cf/-arginine.
Cisltrans isomers may be separated by conventional techniques well known to those skilled in the art, for example, chromatography and fractional crystallisation.
Conventional techniques for the preparation/isolation of individual enantiomers include chiral synthesis from a suitable optically pure precursor or resolution of the racemate (or the racemate of a salt or derivative) using, for example, chiral high pressure liquid chromatography (HPLC).
Alternatively, the racemate (or a racemic precursor) may be reacted with a suitable optically active compound, for example, an alcohol, or, in the case where the compound of formula (I) contains an acidic or basic moiety, a base or acid such as 1-phenylethylamine or tartarlc acid. The resulting diastereomeric mixture may be separated by chromatography and/or fractional crystallization and one or both of the diastereoisomers converted to the corresponding pure enantiomer(s) by means well known to a skilled person.
Chiral compounds of the invention (and chiral precursors thereof) may be obtained in enantiomerically-enrlched form using chromatography, typically HPLC, on an asymmetric resin with a mobile phase consisting of a hydrocarbon, typically heptane or hexane, containing from 0 to 50% by volume of isopropanol, typically from 2% to 20%, and from 0 to
5% by volume of an alkylamine, typically 0.1% diethylamine. Concentration of the eluate affords the enriched mixture.
When any racemate crystallises, crystals of two different types are possible. The first type is the racemic compound (true racemate) referred to above wherein one homogeneous form of crystal is produced containing both enantiomers in equimolar amounts. The second type is the racemic mixture or conglomerate wherein two forms of crystal are produced In equimolar amounts each comprising a single enantiomer.
While both of the crystal forms present in a racemic mixture have identical physical properties, they may have different physical properties compared to the true racemate. Racemic mixtures may be separated by conventional techniques known to those skilled in the art - see, for example, Stereochemistry of Organic Compounds by E. L. Eliel and S. H. Wilen
(Wiley, 1994).
The present invention includes all pharmaceutically acceptable isotopically-labelled compounds of formula (I) wherein one or more atoms are replaced by atoms having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number which predominates In nature.
Examples of isotopes suitable for inclusion in the compounds of the invention include isotopes of hydrogen, such as 2H and 3H, carbon, such as 11C, 13C and 14C, chlorine, such as 36CI, fluorine, such as 18F, iodine, such as 123I and 125I, nitrogen, such as 13N and 16N, oxygen, such as 1SO, 17O and 18O, phosphorus, such as 32P, and sulphur, such as 35S.
Certain isotopically-labelled compounds of formula I, for example, those incorporating a radioactive Isotope, are useful in drug and/or substrate tissue distribution studies. The radioactive isotopes tritium, i.e. 3H, and carbon-14, I.e. 14C, are particularly useful for this purpose in view of their ease of incorporation and ready means of detection.
Substitution with heavier isotopes such as deuterium, i.e. 2H, may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be preferred in some circumstances.
Substitution with positron emitting isotopes, such as "C, 18F, 16O and 13N, can be useful in Positron Emission Topography (PET) studies for examining substrate receptor occupancy.
Isotopically-labeled compounds of formula (I) can' generally be prepared by conventional techniques known to those skilled In the art or by processes analogous to those described in the accompanying Examples and Preparations using an appropriate isotopically-labeled reagent in place of the non-labeled reagent previously employed.
Pharmaceutlcally acceptable solvates in accordance with the invention include those wherein the solvent of crystallization may be isotopically substituted, e.g. D2O, d6-acetone, d6-DMSO.
Also within the scope of the invention are intermediate compounds of formula II as hereinbefore defined, .all salts, solvates and complexes thereof and all solvates and complexes of salts thereof as defined hereinbefore for compounds of formula I. The invention includes all polymorphs of the aforementioned species and crystal habits thereof.
When preparing compounds of formula (I) in accordance with the invention, it is open to a person skilled In the art to routinely select the form of compound of formula II which provides the best combination of features for this purpose. Such features include the melting point, solubility, processability and yield of the intermediate form and the resulting ease with which the product may be purified on isolation.
The compounds of formula (I) should be assessed for their biopharmaceutical properties, such as solubility and solution stability (across pH), permeability, etc., in order to select the most appropriate dosage form and route of administration for treatment of the proposed indication.
Compounds of the invention intended for pharmaceutical use may be administered as crystalline or amorphous products. They may be obtained, for example, as solid plugs, powders, or films by methods such as precipitation, crystallization, freeze drying, spray drying, or evaporative drying. Microwave or radio frequency drying may be used for this purpose.
They may be administered alone or in combination with one or more other compounds of the invention or in combination with one or more other drugs (or as any combination thereof). Generally, they will be administered as a formulation in association with one or more pharmaceutically acceptable excipients. The term 'excipient' Is used herein to describe any ingredient other than the compound(s) of the invention. The choice of excipient will to a large extent depend on factors such as the particular mode of administration, the effect of the excipient on solubility and stability, and the nature of the dosage form.
Pharmaceutical compositions suitable for the delivery of compounds of the present invention and methods for their preparation will be readily apparent to those skilled in the art. Such compositions and methods for their preparation may be found, for example, in Remington's Pharmaceutical Sciences. 19th Edition (Mack Publishing Company, 1995).
The compounds of the invention may be administered orally. Oral administration may involve swallowing, so that the compound enters the gastrointestinal tract, and/or buccal, lingual, or sublingual administration by which the compound enters the blood stream directly from the mouth.
Formulations suitable for oral administration Include solid, semi-solid and liquid systems such as tablets; soft,or hard capsules containing multi- or nano-particulates, liquids, or powders; lozenges (including liquid-filled); chews; gels; fast dispersing dosage forms; films; ovules; sprays; and buccal/mucoadheslve patches.
Liquid formulations include suspensions, solutions, syrups and elixirs. Such formulations may be employed as fillers in soft or hard capsules (made, for example, from gelatin or hydroxypropylmethylcellulose) and typically comprise a carrier, for example, water, ethanol, polyethylene glycol, propylene glycol, methylcellulose, or a suitable oil, and one or more emulsifying agents and/or suspending agents. Liquid formulations'may also be prepared by the reconstitution of a solid, for example, from a sachet.
The compounds of the invention may also be used in fast-dissolving, fast-disintegrating dosage forms such as those described In Expert Opinion in Therapeutic Patents, H (6), 981-986, by Liang and Chen (2001).
For tablet dosage forms, depending on dose, the drug may make up from 1 weight % to 80 weight % of the dosage form, more typically from 5 weight % to 60 weight % of the dosage form. In addition to the drug, tablets generally contain a disintegrant. Examples of disintegrants include sodium starch glycolate, sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, croscarmellose sodium, crospovldone, polyvinylpyrrolidone, methyl cellulose, microcrystalline cellulose, lower alkyl-substituted hydroxypropyl cellulose, starch, pregelatinised starch and sodium aiginate. Generally, the disintegrant will comprise from 1 weight % to 25 weight %, preferably from 5 weight % to 20 weight % of the dosage form.
Binders are generally used to impart cohesive qualities to a tablet formulation. Suitable binders include microcrystalline cellulose, gelatin, sugars, polyethylene glycol, natural and synthetic gums, polyvinylpyrrolidone, pregelatinised starch, hydroxypropyl cellulose and hydroxypropyl methylcellulose. Tablets may also contain diluents, such as lactose (monohydrate, spray-dried monohydrate, anhydrous and the like), mannitol, xylitol, dextrose, sucrose, sorbitol, microcrystalline cellulose, starch and dibasic calcium phosphate dihydrate.
Tablets may also optionally comprise surface active agents, such as sodium lauryl sulfate and polysorbate 80, and glidants such as silicon dioxide and talc. When present, surface active
agents may comprise from 0.2 weight % to 5 weight % of the tablet, and glidants may comprise from 0,2 weight % to 1 weight % of the tablet.
Tablets also generally contain lubricants such as magnesium stearate, calcium stearate, zinc stearate, sodium stearyl fumarate, and mixtures of magnesium stearate with sodium lauryl sulphate. Lubricants generally comprise from 0.25 weight % to 10 weight %, preferably from 0.5 weight % to 3 weight % of the tablet.
Other possible ingredients include anti-oxidants, colourants, flavouring agents, preservatives and taste-masking agents.
Exemplary tablets contain up to about 80% drug, from about 10 weight % to about 90 weight % binder, from about 0 weight % to about 85 weight % diluent, from about 2 weight % to about 10 weight % disintegrant, and from about 0.25 weight % to about 10 weight % lubricant.
Tablet blends may be compressed directly or by roller to form tablets. Tablet blends or portions of blends may alternatively be wet-, dry-, or melt-granulated, melt congealed, or extruded before tabletting. The final formulation may comprise one or more layers and may be coated or uncoated; it may even be encapsulated.
The formulation of tablets is discussed in Pharmaceutical Dosage Forms: Tablets. Vol. 1, by H. Lieberman and L Lachman'(Marcel Dekker, New York, 1980).
Consumable oral films for human or veterinary use are typically pliable water-soluble or water-swellable thin film dosage forms which may be rapidly dissolving or mucoadhesive and typically comprise a compound of formula I, a film-forming polymer, a binder, a solvent, a humectant, a plasticiser, a stabiliser or emulsifier, a viscosity-modifying agent and a solvent. Some components of the formulation may perform more than one function.
The compound of formula (I) may be water-soluble or insoluble. A water-soluble compound typically comprises from 1 weight % to 80 weight %, more typically from 20 weight % to 50 weight %, of the solutes. Less soluble compounds may comprise a greater proportion of the composition, typically up to 88 weight % of the solutes. Alternatively, the compound of formula (I) may be in the form of multiparticulate beads.
The film-forming polymer may be selected from natural polysaccharides, proteins, or synthetic hydrocollolds and is typically present in the range 0.01 to 99 weight %, more typically in the range 30 to 80 weight %.
Other possible ingredients include anti-oxldants, colorants, flavourings and flavour enhancers, preservatives, salivary stimulating agents, cooling agents, co-solvents (including oils), emollients, bulking agents, anti-foaming agents, surfactants and taste-masking agents.
Films in accordance with the invention are typically prepared by evaporative drying of thin aqueous films coated onto a peelable backing support or paper. This may be done in a drying oven or tunnel, typically a combined coaler dryer, or by freeze-drying or vacuuming.
Solid formulations for oral administration may be formulated to be immediate and/or modified release. Modified release formulations Include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.
Suitable modified release formulations for the purposes of the invention are described in US Patent No. 6,106,864. Details of other suitable release technologies such as high energy dispersions and osmotic and coated particles are to be found in Pharmaceutical Technology. On-line. 25(2), 1-14, by Verma et al (2001). The use of chewing gum to achieve controlled release is described in WO 00/35298.
The compounds of the invention may also be administered directly into the blood stream, into muscle, or into an internal organ. Suitable means for parenteral administration include intravenous, intraarterial, intraperitoneal, intrathecal, intraventricular, intraurethral, intrasternal, intracranial, intramuscular, intrasynovial and subcutaneous. Suitable devices for parenteral administration include needle (including microneedle) injectors, needle-free injectors and infusion techniques.
Parenteral formulations are typically aqueous solutions which may contain excipients such as salts, carbohydrates and buffering agents (preferably to a pH of from 3 to 9), but, for some applications, they may be more suitably formulated as a sterile non-aqueous solution or as a dried form to be used in conjunction with a suitable vehicle such as sterile, pyrogen-free water.
The preparation of parenteral formulations under sterile conditions, for example, by lyophilisation, may readily be accomplished using standard pharmaceutical techniques well known to those skilled in the art.
The solubility of compounds of formula (I) used in the preparation of parenteral solutions may be increased by the use of appropriate formulation techniques, such as the incorporation of solubility-enhancing agents.
Formulations for parenteral administration may be formulated to be Immediate and/or modified release. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release. Thus compounds of the invention may be formulated as a suspension or as a solid, semi-solid, or thixotropio liquid for administration as an implanted depot providing modified release of the active compound. Examples of such formulations include drug-coated stents and semi-solids and suspensions comprising drug-loaded poly(o7-lactic-coglycolic)acid (PGLA) microspheres.
i
The compounds of the invention may also be administered topically, (intra)dermally, or transdermally to the skin or mucosa. Typical formulations for this purpose include gels, hydrogels, lotions, solutions, creams, ointments, dusting powders, dressings, foams, films, skin patches, wafers, implants, sponges, fibres, bandages and microemulsions. Liposomes may also be used. Typical carriers include alcohol, water, mineral oil, liquid petrolatum, white petrolatum, glycerin, polyethylene glycol and propylene glycol. Penetration enhancers may be incorporated - see, for example, J Pharm Sci, §8 (10), 955-958, by Finnin and Morgan (October 1999).
Other means of topical administration include delivery by electroporation, iontophoresis, phonophoresis, sonophoresis and microneedle or needle-free (e.g. Powderject™, Bibject™, etc.) injection.
Formulations for topical administration may be formulated to be immediate and/or modified release. Modified release formulations include delayed-,, sustained-, pulsed-, controlled-, targeted and programmed release.
The compounds of the invention can also be administered intranasally or by inhalation, typically in the form of a dry powder (either alone, as a mixture, for example, in a dry blend with lactose, or as a mixed component particle, for example, mixed with phospholipids, such as phosphatidylcholine) from a dry powder inhaler, as an aerosol spray from a pressurised container, pump, spray, atomiser (preferably an atomiser using electrohydrodynamics to produce a fine mist), or nebuliser, with or without the use of a suitable propellant, such as 1,1,1,2-tetrafluoroethane or 1,1,1,2,3,3,3-heptafluoropropane, or as nasal drops. For intranasal use, the powder may comprise a bioadhesive agent, for example, chitosan or cyclodextrin.
The pressurised container, pump,, spray, atomizer, or nebuliser contains a solution or suspension of the compound(s) of the invention comprising, for example, ethanol, aqueous ethanol, or a suitable alternative agent for dispersing, solubilislng, or extending release of the active, a propellant(s) as solvent and an optional surfactant, such as sorbitan trioleate, oleic acid, or an ollgolactic acid.
Prior to use in a dry powder or suspension formulation, the drug product is micronised to a size suitable for delivery by inhalation (typically less than 5 microns). This may be achieved by any appropriate comminuting method, such as spiral jet milling, fluid bed jet milling, supercritical fluid processing to form nanoparticles, high pressure homogenisatlon, or spray drying.
Capsules (made, for example, from gelatin or hydroxypropylmethylcellulose), blisters and cartridges for use in an inhaler or insufflator may be formulated to contain a powder mix of the compound of the invention, a suitable powder base such as lactose or starch and a performance modifier such as /-leucine, mannitol, or magnesium stearate. The lactose may be anhydrous or In the form of the monohydrate, preferably the latter. Other suitable excipients include dextran, glucose, maltose, sorbitol, xylltol, fructose, sucrose and trehalose.
A suitable solution formulation for use in an atomiser using electrohydrodynamics to produce a fine mist may contain from 1(jg to 20mg of the compound of the Invention per actuation and the actuation volume may vary from 1ul to 100ul. A typical formulation may comprise a compound of formula I, propylene glycol, sterile water, ethanol and sodium chloride. Alternative solvents which may be used instead of propylene glycol Include glycerol and polyethylene glycol.
Suitable flavours, such as menthol and levomenthol, or sweeteners, such as saccharin or saccharin sodium, may be added to those formulations of the invention intended for Inhaled/intranasal administration.
Formulations for inhaled/intranasal administration may be formulated to be immediate and/or modified release using, for example, PGLA. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.
In the case of dry powder inhalers and aerosols, the dosage unit is determined by means of a valve which delivers a metered amount. Units in accordance with the Invention are typically arranged to administer a metered dose or "puff1 containing from O.OOImg to 10mg of the compound of formula (I). The overall daily dose will typically be In the range O.OOImg to 40mg which may be administered In a single dose or, more usually, as divided doses throughout the day.The compounds of formula (I) are particularly suitable for an administration by inhalation

The compounds of the invention may be administered rectally or vaginally, for example, in the form of a suppository, pessary, or enema. Cocoa butter is a traditional suppository base, but various alternatives may be used as appropriate.
Formulations for rectal/vaginal administration may be formulated to be Immediate and/or modified release. Modified release formulations Include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.
The compounds of the indention may also be administered directly to the eye or ear, typically in the form of drops of a mlcronised suspension or solution in isotonic, pH-adjusted, sterile saline. Other formulations suitable for ocular and aural administration include ointments, gels, biodegradable (e.g. absorbable gel sponges, collagen) and non-biodegradable (e.g. silicone) Implants, wafers, lenses and particulate or vesicular systems, such as niosomes or liposomes. A polymer such as crossed-linked poiyacrylic acid, polyvinylalcohol, hyaluronic acid, a cellulosic polymer, for example, hydroxypropylmethylcellulose, hydroxyethylcellulose, or methyl cellulose, or a heteropolysaccharide polymer, for
example, gelan gum, may be incorporated together with a preservative, such as benzalkonium chloride. Such formulations may also be delivered by iontophoresis. Formulations for ocular/aural administration may be formulated to be immediate and/or modified release. Modified release formulations Include delayed-, sustained-, pulsed-, controlled-, targeted, or programmed release.
The compounds of the invention may be combined with soluble macromolecular entities, such as cyclodextrin and suitable derivatives thereof or polyethylene glycol-containing polymers, in order to improve their solubility, dissolution rate, taste-masking, bioavailability and/or stability for use in any of the aforementioned modes of administration.
Drug-cyclodextrln complexes, for example, are found to be generally useful for most dosage forms and administration routes. Both inclusion and non-inclusion complexes may be used. As an alternative to direct complexation with the drug, the cyclodextrin may be used as an auxiliary additive, I.e. as a carrier, diluent, or solubiliser. Most commonly used for these purposes are alpha-, beta- and gamma-cyclodextrins, examples of which may be found in International Patent Applications Nos. WO 91/11172, WO 94/02518 and WO 98/55148.
Inasmuch as it may desirable to administer a combination of active compounds, for example, for the purpose of treating a particular disease or condition, it is within the scope of the present invention that two or more pharmaceutical compositions, at least one of which contains a compound in accordance with the invention, may conveniently be combined in the form of a Kit suitable for coadministration of the compositions.
Thus the kit of the invention comprises two or more separate pharmaceutical compositions, at least one of which contains a compound of formula (I) in accordance with the invention, and means for separately retaining said compositions, such as a container, divided bottle, or divided foil packet. An example of such a kit is the familiar blister pack used for the packaging of tablets, capsules and the like.
The kit of the invention is particularly suitable for administering different dosage forms, for example, oral and parenteral, for administering the separate compositions at different dosage intervals, or for titrating the separate compositions against one another. To assist compliance, the kit typically comprises directions for administration and may be provided with a so-called memory aid.
For administration to human patients, the total daily dose of the compounds of the invention is typically in the range 0.001 mg to 5000mg depending, of course, on the mode of administration. For example, oral administration may require a total dally, dose of from 0.1 mg to 1000mg, while an intravenous dose may only require from 0.001 mg to 100mg. The total dally dose may be administered in single or divided doses and may, at the physician's discretion, fall outside of the typical range given herein.
These dosages are based on an average human subject having a weight of about 60kg to 70kg. The physician will readily be able to determine doses for subjects whose weight falls outside this range, such as infants and the elderly:
For the avoidance of doubt, references herein to "treatment" include references to curative,, palliative and prophylactic treatment.
The compounds of formula (I) have the ability to interact with muscarinic receptors and thereby have a wide range of therapeutic applications, as described further below, because of the essential role which muscarinic receptors play in the physiology of all mammals.
Thus the invention relates to the use of the compounds of formula (I) for the manufacture of a medicament for the treatment or the prevention of diseases, disorders, and conditions In which the M3 receptor is involved. The invention further relates to a method of treatment of a mammal, including a human being, with a M3 antagonist including treating said mammal with an effective amount of a compound of the formula (I) or with a pharmaceutically acceptable salt, derived form or composition thereof.
Therefore, a further aspect of the present Invention relates to the compounds of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, for use in the treatment of diseases, disorders, and conditions in which muscarinic receptors are involved. Examples of such diseases, disorders, and conditions are Inflammatory Bowel Disease, Irritable Bowel Disease, divertlcular disease, motion sickness, gastric ulcers,
radiological examination of the bowel, symptomatic treatment of BPH (benign prostatic hyperplasia), NSAID induced gastric ulceration, urinary Incontinence (Including urgency, frequency, urge incontinence, overactive bladder, nocturia and Lower urinary tract symptoms), cycloplegla, mydriatics, parkinsons disease.
More specifically, the present invention also concerns the compounds of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, for use in the treatment of diseases, disorders, and conditions selected from the group consisting of:
• chronic or acute bronchoconstriction, chronic bronchitis, small airways obstruction,
and emphysema,
• obstructive or inflammatory airways diseases of whatever type, etiology, or
pathogenesis, in particular an obstructive or inflammatory airways disease that is a
member selected from the group consisting of chronic eosinophilic pneumonia,
chronic obstructive pulmonary disease (COPD), COPD that includes chronic
bronchitis, pulmonary emphysema or dyspnea associated or not associated with
COPD, COPD that is characterized by irreversible, progressive airways obstruction,
adult respiratory distress syndrome (ARDS), exacerbation of airways hyper-reactivity
consequent to other drug therapy and airways disease that is associated with
pulmonary hypertension,
• bronchitis of whatever type, etiology, or pathogenesis, in particular bronchitis that is a
member selected from the group consisting of acute bronchitis, acute laryngotracheal
bronchitis, arachldic bronchitis, catarrhal bronchitis, croupus bronchitis, dry bronchitis,
infectious asthmatic bronchitis, productive bronchitis, staphylococcus or streptococcal
bronchitis and vesicular bronchitis,
• asthma of whatever type, etiology, or pathogenesis, in particular asthma that is a
member selected from the group consisting of atopic asthma, non-atoplc asthma,
allergic asthma, atopic bronchial IgE-mediated asthma, bronchial asthma, essential
asthma, true asthma, intrinsic asthma caused by pathophysiologic disturbances,
extrinsic asthma caused by environmental factors, essential asthma of unknown or
inapparent cause, non-atopic asthma, bronchitic asthma, emphysematous asthma,
exercise-induced asthma, allergen induced asthma, cold air induced asthma,
occupational asthma, Infective asthma caused by bacterial, fungal, protozoa!, or viral
infection, non-allergic asthma, incipient asthma, wheezy infant syndrome and
bronchfolytis,
• acute lung injury,
• bronchiectasis of whatever type, etiology, or pathogenesis, in particular
bronchiectasis that is a member selected from the group consisting of cylindric
bronchiectasis, sacculated bronchiectasis, fusiform bronchiectasis, capillary
bronchiectasis, cystic bronchiectasis, dry bronchiectasis and follicular bronchiectasis.
More specifically, the present Invention also concerns the compounds of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, for use in the treatment of COPD or asthma.
Suitable examples of other therapeutic agents which may be used in combination with the compound(s) of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, include, but are by no means limited to:
(a) 5-Llpoxygenase (5-LO) Inhibitors or 5-lipoxygenase activating protein (FLAP) antagonists,
(b) Leukotriene antagonists (LTRAs) including antagonists of LTB4, LTC4, LTD4, and LTE4,
(c) Histamine receptor antagonists including H1 and H3 antagonists,
(d) α1 and α2-adrenoceptor agonist vasoconstrictor sympathomimetic agents for
decongestant use,
(e) short or long acting pa agonists,
(f) PDE inhibitors, e.g. PDE3, PDE4 and PDE5 inhibitors,
(g) Theophylline,
(h) Sodium cromoglycate,
(i) COX inhibitors both non-selective and selective COX-1 or COX-2 inhibitors (NSAIDs),
(j) Oral and inhaled glucocorticosteroids,
(k) Monoclonal antibodies active against endogenous inflammatory entities,
(1) Anti-tumor necrosis factor (anti-TNF-a) agents,
(m) Adhesion molecule inhibitors including VLA-4 antagonists,
(n) Kinin-B! - and Bz-receptor antagonists,
(o) Immunosuppressive agents,
(p) Inhibitors of matrix metalloproteases (MMPs),
(q) Tachykinln NK1 NK2 and NK3 receptor antagonists,
(r) Elastase inhibitors,
(s) AdenosineA2a receptor agonists,
(t) Inhibitors of urokinase,
(u) Compounds that act on dopamine receptors, e.g. D2 agonists,
(v) Modulators of the NFKB pathway, e.g. IKK inhibitors,
(w) modulators of cytokine signalling pathyways such as p38 MAP kinase or syk kinase,
(x) Agents that can be classed as mucolytlcs or anti-tussive,
(y) Antibiotics,
(2) HDAC inhibitors, and,
(aa)PI3 kinase inhibitors.
(bb)CXCR2 antagonists.
According to the present invention, combination of the compounds of formula (I) with :
- H3 antagonists,
- p2 agonists,
- PDE4 inhibitors,
- steroids, especially glucocortlcosteroids,
- Adenosine A2a receptor agonists,
- Modulators of cytokine signalling pathyways such as p38 MAP kinase or syk kinase, or,
- Leukotriene antagonists (LTRAs) including antagonists of LTB4, LTC4, LTD4| and LTE4,
are preferred.
According to the present Invention, combination of the compounds of formula (I) with ;
- glucocorticosteroids, In particular inhaled glucocortlcosteroids with reduced
systemic side effects, including prednisone, prednlsolone, flunisolide,
triamcinolone acetonide, beclomethasone dipropionate, budesonide, fluticasone
proplonate, ciclesonide, and mometasone furcate, or
- ß2 agonists including in particular salbutamol, terbutaline, bambuterol, fenoterol,
salmeterol, formoterol, tulobuterol and their salts.
are further preferred.
The following examples illustrate the preparation of the compounds of the formula (I):
Preparation 1
tert-Butvl 4-cvano-4.4-dlPhenvlbutanoate
A suspension of diphenylacetonitrile (38.6g, 200mmol) in tert-butanol (200ml) was warmed to
60°C for 30 minutes. The resulting solution was cooled to 50°C and a solution of potassium
hydroxide (0.6g, 10.69mmol) in methanol (2mL) was added. tert-Butyl acrylate (30mL,
200mmol) was then added dropwise and the mixture was stirred at 50"C for 2 hours and at
room temperature for 18 hours. Further potassium hydroxide (0.6g, 10.69mmol) was added
and the mixture was re-warmed to 50°C for 3 hours. The reaction mixture was then
concentrated in vacuo and the residue was diluted with diethyl ether (300ml), washed with
water (200mL), dried over sodium sulfate and concentrated in vacuo to afford the title
compound as a white solid in 90% yield, 57.95g.
1HNMR(400MHz, CD3OD) 5: 1.41(s, 9H), 2.29(t, 2H), 2.72(t, 2H), 7.29-7.33(m, 1H), 1H),
7.36-7.42(m, 9H); LRMS APCI m/z 322 [M+H]+
Preparation 2
4-Cvano-4,4-diphenvlbutanoic acid
A mixture of the product of preparation 1 (57.5g, 179.13mmol) in hydrochloric acid (4N in
dioxan, 500mL) was stirred at room temperature for 18 hours. The reaction mixture was
concentrated in vacuo and the residue was treated with warm diisopropyl ether (150mL) then
cooled to room temperature. The resulting solid was filtered off, washing through with
diisopropyl ether (2x30mL), and dried under vacuum to afford the title compound as
crystalline white solid In 77% yield, 36.45g.
1HNMR(400MHz, CD3OD) 6: 2.35(t, 2H), 2.76(t, 2H), 7.30-7.44(m, 10H); LRMS APCI m/z 266
Preparations
tert-B'utyl (3S)-3-phenoxvpvrrolldlne-1 -carboxylate
Disopropylazodicarboxylate (5.7mL, 29.38mmol) was added to an ice-cooled solution of (R)-(-)-N-boc-3-pyrroIidinol (5g, 26.71 mmol), phenol (2.51 g, 26.71 mmol) and trlphenyl phosphine (7.71g, 29.38mmol) in tetrahydrofuran (70mL) and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated in vacuo and the residue was twice triturated with diethyl ether and filtered. The filtrate was washed with 1N sodium hydroxide solution (20mL), dried over sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethyl acetate, 90:10 to 83:17, afforded the title compound as a colourless oil in 75% yield, 5.27g. 1HNMR(400MHz, CD3OD) 5: 1.45(m, 9H), 2.10-2.16(m, 2H), 3.40-3.59(m, 4H), 4.95-4.97(m, 1H), 6.88-6.95(m, 3H), 7.24-7.28(m, 2H)
Preparation 4
tert-Butvl (3S)-3-(3-methoxyphenoxv)pyrrolidlne-1-carboxylate
The title compound was prepared from (R)-(-)-N-boc-3-pyrrolidinol and 3-methoxyphenol,
using the same method as that described for preparation 3, as a gum in 81% yield.
1HNMR(400MHz, CD3OD) 5: 1.45(m, 9H), 2.14(bs, 2H), 3.40-3.58(m, 4H), 3.75(s, 3H),
4.95(m, 1H), 6.45-6.54(m, 3H), 7.14-7.18(m, 1H)
Preparation 5
tert-Butvl(3S)-3-(benzyloxv)pvrrolidine-1-carboxvlate
Sodium hydride (60% dispersion In mineral oil, 2.13g, 53.41 mmol) was added portlonwise to an ice-cooled solution of (S)-(-)-N-boc-3-pyrrolidinol (10g, 53.41 mmol) in tetrahydrofuran (100mL) and the mixture was stirred at 0°C for 1 hour. Benzyl bromide (6.4mL, 53.41 mmol) and tetrahydrofuran (50mL) were added and the mixture was stirred for 6 hours allowing the temperature to rise to 25°C. The reaction mixture was then slowly diluted with water (50mL), concentrated in vacuo and the aqueous residue was extracted with ethyl acetate (3x70mL). The combined organic solution was washed with brine (30mL), dried over sodium sulfate and concentrated in vacuo to give an orange oil. This oil was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 90:10:1. The appropriate, fractions were evaporated under reduced pressure and the residue was further purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 66:33, to afford the title compound as a colourless oil in 74% yield, 10.93g.
1HNMR(400MHz, CD3OD) 5: 1.45(s, 9H), 1.91-2.00(m, 1H), 2.02-2.08(m, 1H), 3.35-3.44(m, 4H), 4.13-4.17(m, 1H), 4.51-4.52(m, 2H), 7.24-7.29(m, 1H), 7.30-7.32(m, 4H); LRMS APCI m/z 278 [M+H]+
preparation 6
tert-Butvl (3R)3-(benzvloxvtovrrolidlne-1 -carboxvlate
The title compound was prepared from (R)-(-)-N-boc-3-pyrrolidinol and benzyl bromide, using the same method as that described for preparation 5. The crude compound was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, to afford the desired product in 97% yield.
1HNMR(400MHZ, CD3OD) 5: 1.48(8, 3H), 1.92-2.02(m, 1H), 2.03-2.10(m, 1H), 3.35-3.48(m, 4H), 4.14-4.19(m, 1H), 4.49-4.57(m, 2H), 7.24-7.33(m, 5H)
Preparation 7
(3S)3-PhenoxvDvrrolidinehvdrochloride
A mixture of the product of preparation 3 (5.25g, 19.96mmol) in hydrochloric acid (4N in
dioxan, 50mL) was stirred at room temperature for 2 hours. The reaction mixture was then
concentrated in vacuo to afford the title compound as a white solid in 100% yield.
1HNMR(400MHz, CD3OD) 6: 2.29-2.33(m, 2H), 3.42-3.56(m, 4H), 5.18-5.21(m, 1H), 6.95-
7.01(m, 3H), 7,29-7.32(m, 2H); LRMS APCI m/z 164 [M+H]+
Preparation 8
(3S)3-(3-MBthoxvphenoxvtovrrolidine
A mixture of the product of preparation 4 (3.19g, 10.8mmol) In hydrochloric acid (4N in
dioxan, 27mL) was stirred at room temperature for 3 hours. The reaction mixture was then
concentrated in vacuo and the residue was purified by column chromatography using an
Isolute® SCX-2 cartridge, eluting with methanol followed by 1M ammonia in methanol, to
afford the title compound as a yellow oil in 85% yield, 1 J7g.
1HNMR(400MHz, CD3OD) 5: 1.91-1.98(m, 1H), 2.02-2.11(m, 1H), 2.85-2.91(m, 1H), 3.02-
3.08(m, 3H), 3.75(s, 3H), 4,85-4.89(m, 1H), 6.43-6.51(m, 3H), 7.12-7.16(m, 1H);.LRMS APCI
m/z194[M+H]+
Preparation 9
(3S)-3-(Ben2ylgxy)pvrrolldinehvdrochlorlde
The title compound was prepared from the product of preparation 5, using the same method
as that described for preparation 7, as a solid in 100% yield.
1HNMR(400MHz, CD3OD) 6: 2.02-2.12(m, 1H), 2.22-2.29(m, 1H), 3.26-3.46(m, 4H), 4.35-
4.37(m, 1H), 4.55(s, 2H), 7.25-7.37(m, 5H); LRMS APCI m/z 178 [M+H]+
Preparation 10
(3RV3-(Benzylox\rtpvrrolldinehvdrochloride
The title compound was prepared from the product of preparation 6, using the same method
as that described for preparation 7, as a solid in 100% yield.
1HNMR(400MHz, CDCI3) 6: 1.96-2.05(m, 1H), 2.20-2.15(m, 1H), 3.49-3.32(m, 4H), 4.23-
4.25(m, 1H), 4.44-4.54(m, 2H), 7.26-7.36(m, 5H), 9.74-9.88(m, 2H); LRMS APCI m/z 178
Preparation 1 1
5-Oxo-5-ff3S)-3-phenoxvDvrrolidin-1-yl]-2.2-diphenvlpentanenltrile
A mixture of the products of preparations 2 (2.40g, 9.05mmol) and 7 (1.99g, 9.96mmol), 1-(3-
dimethylaminopropyl)-3-ethylcarbodlimide hydrochloride (1.55g, 9.96mmol), 1-
hydroxybenzotriazole hydrate (1.35g, 9.96mmol) and triethylamine (1.38mL, 9.96mmol) in
dichloromethane (40mL) was stirred at room temperature for 18 hours. The reaction mixture
was then diluted with dichloromethane (100mL), washed with 1M hydrochloric acid (70mL),
1M sodium hydroxide solution (30mL) and brine (30mL), dried over sodium sulfate and
concentrated in vacuo. The residue was re-crystallised from hot ethanol to afford the title
compound as a crystalline solid in 76% yield, 2.83g.
1HNMR(400MHz, CD3OD) 5: 2.07-2.21(m, 2H), 2.33-2.38(m, 1H), 2.43-2.47(m, 1H), 2.69-
2.84(m, 2H), 3.44-3.55(m, 2H), 3.58-3.67(m, 2H), 4.96-5.04(m, 1H), 6.89(d, 2H), 6.93-6.96(m,
1H), 7.24-7 ,46(m, 12H); LRMS APCI m/z 412 [M+H]+
Preparation 12
5-Oxo-5-[(3R)-3-phenoxvpvrrolidin-1-yl]2.2-dlprienvlpentanenitrile
The title compound was prepared from (3R)-3-phenoxypyrrolidine (WO 2005/061457) and the
product of preparation 2, using the same method as that described, for preparation 1 1 , to
afford the title compound in 41% yield.
Preparation 13
5-[(3S)3-(3-Methoxyphenoxy)pyrrolldin-1-yl]-5-oxo-2.2-dlphenvlpentanenitrile The title compound was prepared from the products of preparations 2 and 8, using the same method as that described for preparation 11. The crude compound was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 98:2:0.2 to 95:5:0.5, to afford the desired product as a colourless oil in quantitative yield. 1HNMR(400MHz, CD3OD) 6: 2.03-2.20(m, 2H), 2.32-2.37(m, 1H), 2.43-2.47(m, 1H), 2.66-2.84(m, 2H), 3.44-3.67(m, 4H), 3.74(s, 3H), 4.94-5.00(m, 1H), 6.44-6.55(m, 3H), 7.13-7.1 9(m, 1H), 7.28-7.46(m, 10H); LRMS APCI m/z 412 [M+HJ*
Preparation 14
5-[(3S^3-fBenzvloxv)pvrrolidln-1-vl1-5-oxo-2.g-diphenvlpentanenitrile
The title compound was prepared from the products of preparation 2 and 9, using the same
method as that described for preparation 1 1, as a pale orange solid in 70% yield.
1HNMR(400MHz, CD3OD) 5: 1.86-2.15(m, 2H), 2.32-2.43(m, 2H), 2.75-2.82(m, 2H), 3.35-
3.62(m, 4H), 4.14-4.21(m, 1H), 4.45-4.56(m, 2H), 7.22-7.44(m, 15H);LRMS APCI m/z 412
Preparation 15
5-{3R)-3-(Benzvloxy^pvrrolldirj-1-yl1-5-oxo-2.2-dlphenvlDentanenitrile N.N'-Carbonyldiimldazole (27g, 162mmol) was added to a solution of the product of preparation 2 (38g, 135mmol) in tetrahydrofuran (600mL) and the mixture was stirred for 3 hours at room temperature. A solution of the product of preparation 10 (31g, 141.75mmol) in tetrahydrofuran (300ml) was added and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then filtered, washing through with tetrahydrofuran, and the filtrate was concentrated in vacuo. The residue was partitioned between water (200mL) and ethyl acetate (600mL) and the organic layer was separated, washed with water, 2N hydrochloric acid (2x100mL) and brine, dried over magnesium sulfate and concentrated in vacuo. Trituration of the residue with dlethyl ether then afforded the title compound in 83% yield, 48.2g.
1HNMR(400MHz, CD3OD) 6: 1.87-2.15(m, 2H), 2.32-2.44(m, 2H), 2,74-2.82(m, 2H), 3.35-3.61 (m, 4H), 4.14-4.22(m, 1H), 4.46-4.57(m, 2H), 7.23-7.44(m, 15H); LRMS APCI m/z 425 [M+H]+
Preparation 16
54(3S)-3-Hvdroxvpvrrolldln-1-yl]-5-methvl-2.2-dlphenvlhexanamide
Iron (III) chloride (1.57g, 9.70mmol) was added to a solution of the product of example 11
(385mg, 0.84mmol) in dlchloromethane (10mL) and the mixture was stirred at room
temperature for 3 hours. The reaction was quenched by the addition of 2M hydrochloric acid
(6mL), filtered through Arbocel® and the filtrate was basified with 0.88 ammonia solution
(20mL). The layers of the filtrate were separated and the aqueous solution was extracted with
dichloromethane (2x25mL). The combined organic solution was dried over sodium sulfate,
concentrated in vacuo and purification of the residue by column chromatography on silica gel,
eluting with ethyl acetate:methanol:0.88 ammonia, 95:5:0.5 to 85:15:1.5, afforded the title
compound as a brown gum in 60% yield, 415mg.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 6H), 1.23-1.27(m, 2H), 1.56-1.64(m, 1H), 1.89-1.98(m,
1H), 2.40-2.44(m, 3H), 2.47-2.52(m, 1H), 2.61-2.67(m, 1H), 2.74-2.78(m, 1H), 4.l7-4.22(m,
1H), 7.22-7.26(m, 2H), 7.29-7.33(m, 4H), 7.37(d, 4H); LRMS APCI m/z 367 [M+H]+
Preparation 17
S-K3RV3-HvdrQXVDvrrolidin-1-vl1-S-methvl-2.2-dlphenvlhexanarnide 1N Hydrochloric acid (10.95mL, 10.95mmol) and 20% Pd(OH)2 (1g) were added to a solution of the product of example 9 (5g, 10.95mmol) in ethanol (250mL) and the mixture was stirred at 50°C, under 50 psi of hydrogen gas, for 4 hours. The reaction mixture was then filtered through Arbocel® and the filtrate was concentrated in vacuo to give a white foam. The foam was re-dissolved in ethanol (250mL), 20% Pd(OH)2 (1g) was added and the mixture was stirred at 50°C, under 50psi of hydrogen gas, for 24 hours. The reaction mixture was then filtered.through Arbocel®, washing through with ethanol, and the filtrate was concentrated in vacuo. The residue was suspended in 0.88 ammonia, extracted with ethyl acetate (3 x50mL)
and the combined organic solution was washed with brine (50mL), dried over sodium sulfate and concentrated in vacuo to afford the title compound as a white foam in 90% yield, 3.63g. 1HNMR(400MHz, CD3OD) 5: 0.99(s, 6H), 1.23-1.27(m, 2H), 1.56-1.63(m, 1H), 1.89-1.96(m, 1H), 2.39-2.44(m, 3H), 2.46-2.52(m, 1H), 2.61-2.67(m, 1H), 2.74-2.78(m, 1H), 4.17-4.22(m, 1H), 7.22-7.26(m, 2H), 7.29-7.33(m, 4H), 7.36-7.39(m, 4H); LRMS APCI m/z 367 [M+H]+
Preparation 18
5-[(3S)-3-Hvdroxvpvrrolldin-1-yl]-5-methvl-2.2-diphenvlhexanenitrlle
Iron (III) chloride (1.33g, 8.22mmol) was added to a solution of the product of example 10
(1.2g, 2.74mmol) in dichloromethane (25mL) and the mixture was stirred at room temperature
for 3 hours. The solvent was removed in vacuo and the residue was partitioned between 2M
hydrochloric acid (aq) (20mL) and diethyl ether (30mL). The aqueous layer was separated
and baslfied to pH14 with solid sodium hydroxide. The resulting brown precipitate was
collected by filtration and purified by column chromatography on silica gel, eluting with
dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 85:15:1.5, to afford the title compound
as a colourless gum in 50% yield, 475mg.
1HNMR(400MHz, CD3OD) 5: 1.11(8, 6H), 1.52-1.56(m, 2H), 1.69-1.76(m, 1H), 1.95-2.04(m,
1H), 2.53-2.57(m, 2H), 2.62-2.65(m, 1H), 2.69-2.76(m, 1H), 2.83-2.95(m, 2H), 4.27-4.31 (m,
1H), 7.29-7.33(m, 2H), 7.36-7.45(m, 8H); LRMS APCI m/z 349 [M+H]+
Preparation 19
5-{(3S)-3-[(6-([tert-Butvl(dimethvl)silvnoxv}-2-naDhthvhoxv]Pvrrolidin-1-vft-5-methyl-2.2-diphenvlhexanamide
1,1l-Azobis(N,N'-dimethylformamide) (95mg, 0.553mmol) was added to an ice-cooled solution of triphenyl phosphine (145mg, 0.553mmol), 6-(tert-Butyldimethylsilyloxy)-2-naphthol t(102mg, 0.372mmol) EP625510, p13] and the product from preparation 17 (150mg, 0.41 mmol) in tetrahydrofuran (5mL) and the mixture was heated at 60°C for 18hrs. Additional triphenyl phosphine (145mg, 0.553mmol) and 1,1I-Azobis(N,Nl-dimethylformamide) (95mg, 0.553mmol) were added and heating continued for a further 18hrs. The mixture was concentrated In vacuo and the residue purified using an Isolute® SCX-2 cartridge, eluting with methanol, then with 0.25M ammonia in methanol, Basic fractions were concentrated In vacuo and further purified using a RediSep* silica gel cartridge, eluting with dichloromethane: methanol:0.88 ammonia (100:0:0 to 92:8:0.8) to afford the title compound in 20% yield, 46mg, 1HNMR(400MHz, CD3OD) 5: 0.24(s, 6H), 0.95(s, 3H), 1.04(s, 9H), 1.06(s, 3H) 1.15-1.29(m, 2H), 1.88-1.99(m, 1H), 2.11-2.22(m, 1H), 2.30-2.52(m, 2H), 2.54-2.62(m, 1H), 2.64-2.69(m, 1H), 2.72-2.82(m, 1H), 2.82-2.90(m, 1H), 4.83-4.89(m, 1H), 6.96-7.06(m, 2H), 7.12-7.34(m, 12H), 7.53-7.57(m, 1H), 7.60-7.65(m, 1H); LRMS APCI m/z 623 [M+H]+
Preparation 20 5-[(3R)-3.Hvdroxvovrrolldln-1-yl]-5-methvl-2.2-diPh6nylhexanenitrile
Iron (III) chloride (13.3g, 82.192mmol) was added to a solution of the product of example 8 (9g, 20.548mmol) in diohioromethane (200mL) and the mixture was stirred at room temperature for 1 hour. The reaction, was quenched by addition of 2M hydrochloric acid (150mL) and stirred for 30 minutes. The organic layer was separated and the aqueous re-extracted with a further 100ml dichloromethane. The combined organic layers were dried over sodium sulphate and concentrated In vacuo. Purification by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 90:1:1.0, afforded the title compound as a pale brown foam in 89% yield, 6.37g.
1HNMR(400MHz, CD3OD) 5: 1.18(s, 6H), 1.58-1.62(m, 2H), 1.76-1.84(m, 1H), 1.96-2.05(m, 1H), 2.55-2.59(m, 2H), 2.74-2.81(m, 1H), 2.87-2.93(m, 1H), 2.98-3.06(m, 2H), 4.32-4.36(m, 1H), 7.30-7.34(m, 2H), 7.37-7.46(m, 8H); LRMS APCI m/z 349 [M+H]+
Preparation 21 2-Chloro-3-Methoxyhhenol
3-Chloroperoxybenzoic acid (760mg, 4.396mmol) was added portionwise to a solution of 2-Chloro-3-Methoxybenzaidehyde (500mg, 2.931 mmol) in dichloromethane (12ml) and the mixture was stirred for 3 hours at room temperature. Further 3-chloroperoxybenzolc acid (760mg, 4.396mmol) was added and mixture allowed to stir for 18hrs. The solution was diluted with 12ml dichloromethane and washed with saturated sodium sulphite solution (15ml) and saturated sodium hydrogen carbonate solution (15ml). The organic layer was dried over sodium sulphate and concentrated in vacuo to a yellow gum. The residue was dissolved in methanol (12ml), triethylamine (0.05ml) was added and the mixture stirred for 18 hours at room temperature. The solution was concentrated in vacuo, dissolved In diethyl ether (20ml) and extracted with 1N sodium hydroxide (20ml). The aqueous layer was acidified to pH1 by dropwise addition of 2N hydrochloric acid and extracted with diethyl ether (2x25ml). These combined organic layers were dried over sodium sulphate and concentrated in vacuo to afford the title compound as a brown gum in 70% yield, 325mg. 1HNMR(400MHz, CD3OD) 5δ: 3.83(s, 3H), 6.52-6.54(d, 2H), 7.01-7.06(t, 1H)
Preparation 22
1-Chloro-3-Fluoro-2-Methoxvbenzene
Methyl iodide (850)1.1, 13.646mmol) and potassium carbonate (943mg, 6.824mmol) were
added to 2-chloro-6-fluorophenol (1.0g, 6.824mmol) in tetrahydrofuran (10ml) and the mixture
was stirred at room temperature for 3 hours. The reaction mixture was partitioned between
diethyl ether (50ml) and water (50ml). The organic phase was extracted and further washed
with water (2 x 20ml) then dried over sodium sulphate and concentrated in vacuo to afford the
title compound as a colourless liquid in 94% yield, 1.03g.
1HNMR(400MHz, CD3OD) 6: 3.90-3.91(s, 3H), 7.01-7.12(m, 2H), 7.1
Preparation 23
3-Ftuoro-5-MethoxvphenQl
Boron tribromide (1M in dichloromethane, 9rnL, 89.985mmol) was added drop wise to an ice-
cooled solution of 3,5-dimethoxy fluorobenzene (3ml, 22.496mmol) in dichloromethane
(20mL) and the mixture was stirred at 0°C to room temperature for 4 hours. The solution was
cooled to 0°C, further boron tribromide (4ml, 44.992mmol) was added and stirring continued,
warming to room temperature for an additional 18 hours. The reaction was quenched with
0.88 ammonia solution and stirred at room temperature for 90 minutes. The organic layer was
separated and extracted with 2N sodium hydroxide (30ml), which was then acidified to pH1 by
drop wise addition of concentrated hydrochloric acid. The aqueous layer was then re-
extracted with dichloromethane (3x1 5mL), the combined organic solution was dried over
sodium sulfate and concentrated in vacuo to afford the title compound as a white solid in 54%
yield, 1.72g.
1HNMR(400MHz, CD3OD) 6: 3.72(s, 3H), 6.07-6.15(m, 3H)
Preparation 24
1-Fluoro-3-Methoxv-5-Trifluoromethvl-benzene
The title compound was prepared from 3-fluoro-5-trifluoromethylphenol, using the same
method as that described for preparation 22 to afford a colourless oil in 90% yield.
1HNMR(400MHz, CD3OD) 6: 3.84(s, 3H), 6.92-6.97(m, 2H), 7.00(s,
Preparation 25
4-Fluoro-3-Methoxvphenol
The title compound was prepared from 4-fluoro-3-methoxybenzaldehyde, using the same
method as that described for preparation 21 , to afford a brown oil in 55% yield.
1HNMR(400MHz, CD3OD) 5: 3.79(s, 3H), 6.23-6.27(m, 1H), 6.47-6.50(dd, 1H), 6.81-6.86(m,
1H)
Preparation 26
2-Fluoro-3-ly1ethoxvphenol
The title compound was prepared from 2-fluoro-3-methoxybenzaldehyde, using the same
method as that described for preparation 21, to afford a brown oil in 33% yield.
1HNMR(400MHz, CD3OD) 5: 3.82(s, 3H), 6.47-6.55(m, 2H), 6.82-6.87(t, 1H)
Preparation 27
1-Allvloxv-3-bromomethvl-benzene
To a solution of (3-allyloxy-phenyl)-methanol (Tetrahedron, 2000, 56(13), 1873-1882) (1.07g,
6.49mmol) in THF (7mls) at 3°C was added carbon tetrabromide (2.69g, 8.11 mmol) then
trlphenylphosphine (2.1 3g, 8. 11 mmol) In THF (2mls). The reaction mixture was stirred at 5°C
for 1 hour. The reaction mixture was filtered and concentrated in vacuo. The residue was

washed with pentane to give a yellow solid which was purified by column chromatography on silica gel, eluting with pentaneiethyl acetate, 100:0, to 95:5 to afford the title compound as a pale yellow oil in 24% yield, 350mg.
1HNMR(400MHz, CDCI3) 5: 4.47 (s, 2H),~ 4,51-4.60 (m, 2H), 5.26-5.35 (m, 1H), 5.37-5.47 (m, 1H), 5.99-6.11 (m, 1H), 6.82-6.90 (m, 1H), 6.92-7.01 (m, 2H), 7.21-7.30 (m, 1H).
Preparation 28
5-[(3RV3-(3-Allvloxv-benzvloxv)-Pvrrolidln-1-vl1-5-methvl-2.2-dlphenvl-hexanenitrile The product of preparation 20 (179mg, 0.514mmol) In dimethylformamide (3ml) was added drop wise to an ice-cooled solution of sodium hydride (60% dispersion in mineral oil, 31 mg, 0.770mmol) in dimethylformamide (1ml). After stirring for 1 hour the product of preparation 27 (175mg, 0.514mmol) in dimethylformamide (1ml) was added and the mixture was allowed to warm to room temperature for 18 hours. The reaction mixture was then re-cooled to 0°c and further sodium hydride (60% dispersion in mineral oil, 31 mg, 0.770mmol) added, with stirring at room temperature for an additional 3 hours. The solution was quenched by dropwise addition of water, concentrated in vacuo and partitioned between ethyl acetate (1 Oml) and water (10ml). The organic layer was extracted and washed with water (10ml), then dried over sodium sulphate and concentrated in vacuo. Purification by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 97:3:0.3, afforded the title compound as a pale yellow gum in 43% yield; 108mg.
1HNMR(400MHz, CDaOD) 5: 1.03(8, 3H), 1.05(s, 3H), 1.44-1.51 (m, 2H), 1.78-1.85(m, 1H), 1.93-2.01 (m, 1H), 2.50-2.55(m, 3H), 2.64-2.78(m, 3H), 4.03-4.08(m, 1H), 4.43(s, 2H), 4.50-4.55(m, 2H), 5.20-5.24(m, 1H), 5.34-5.41 (m, 1H), 5.98-6.09(m, 1H), 6.79-6.84(m, 1H), 6.87-6.94(m, 2H), 7.18-7.21(t, 1H), 7.26-7.43(m, 10H); LRMS ESI m/z495 [M+H]+
Preparation 29
S-Methvl-2,2-diphenvl-5-[(3R)-3-(3-propenyloxv-benzvloxv)-pyrrolidin-1-yl]-hexanoicacid
amide
The title compound was prepared from the product of preparation 28, using the same method
as that described for example 2, with the addition of further potassium hydroxide (2eq) after
20 hours and continued heating for an additional 4hrs to afford product as a yellow gum in
88% yield.
1HNMR(400MHz, CD3OD) 6: 0.99(8, 3H), 1.01(8, 3H), 1.23-1.28(m, 2H), 1.67-1.69(d, 3H),
1.74-1 .B2(m, 1H), 1.88-1.95(m, 1H), 2.40-2.44(m, 2H), 2.47-2.53(m, 1H), 2.55-2.74(m, 3H),-
3.99-4.04(m, 1H), 4.42(s, 2H), 4.85-4.87(m, 1H), 6.40-6.42(d, 1H), 6.88-6.90(d, 1H), 6.96-
6.99(m, 2H), 7.21-7.38(m, 11H); LRMS ESI m/z 513 [M+H]+
Preparation 30 3-Allvloxv-4-fluoro-benzolc acid allvl ester
Allyl bromide (3.04ml, 35.2mmol) was added dropwise to a suspension of 4-fluoro-3-.hydroxybenzoic acid (2.5g, 16.0mmol) and potassium carbonate (4.43g, 32.03mmol) In dimethylformamide (50ml) at room temperature and the mixture was stirred for 18hrs. The solvent was removed In vacuo and the residue partitioned between dlethyl ether (30ml) and water (30ml). The aqueous layer was separated and extracted with further diethyl ether (2 x 20ml). The combined organic layers were washed with water (3 x 10ml), dried over sodium sulfate and concentrated in vacuo to afford the title compound as a colourless liquid in 100% yield, 3.82g.
1HNMR(400MHz, CDCI3) 5: 4.65-4.66(d, 2H), 4.80-4.82(d, 2H), 5.28-5.48(m, 4H), 5.98-6.12(m, 2H), 7.10-7.14(dd, 1H), 7.65-7.69(m, 2H); LRMS APCI m/z 237 [M+H]+
Preparation 31
(3-Allvloxv-4-fluoro-prienvft-methanol
A solution of the product of preparation 30 (2.0g, 8.47mmol) in tetrahydrofuran (30ml) was added dropwise over 20 minutes to a solution of lithium aluminium hydride in tetrahydrofuran (1M, 16.9m), 16.9mmol) at 0°C under a nitrogen atmosphere, and the solution allowed to warm to room temperature over 5hrs. The mixture was cooled 19 0°C and quenched by. sequential dropwise addition of water (1ml), aqueous sodium hydroxide solution (2M, 2ml) and water (3ml), and the mixture stirred at room temperature for 18hrs. The mixture was filtered through Celite® and the filter pad washed with ethyl acetate (3 x20ml). The filtrate was separated and the organic layer washed with brine (10ml), dried over sodium sulfate and concentrated In vacuo to afford the title compound as a colourless liquid in 100% yield, 1.75g. 1HNMR(400MHz, CDCI3) 5: 4.61-4.63(m, 4H), 5.29-5.32(d, 1H), 5.41-5.45(d, 1H), 6.02-6.11(m, 1H), 6.85-6.89(m, 1H), 7.00-7.07(m, 2H); LRMS APCI m/z 165 [M-OHf
Preparation 32
2-Allvloxv-4-bromomethvl-1-fluorobenzene
Dibromotriphenylphosphorane (2,3g, 5.43mmol) was added to a solution of the product from
preparation 31 (900mg, 4.94mmol) In acetonitrile (40ml) at room temperature and the solution
stirred for 18hrs. The solvent was removed in vacuo and the residue purified by column
chromatography on silica gel, eluting with pentane:ethyl acetate (80:20) to afford the title
compound as a colourless liquid in 31 % yield, 380mg.
1HNMR(400MHz, CDCI3) 5: 4.44(s, 2H), 4.61-4.63(m, 2H), 5.30-5.34(m, 1H), 5.41-5.47(m,
1H), 6.02-6.11(m, 1H), 6.91-6.94(m, 1H), 6.99-7.05(m, 2H); LRMS APCI m/z 165 [M-Br]+
Preparation 33
5-[(3R)-3-(3-Allvloxv-4-fluoro-benzvloxv)-pvrrolidln-1-yl]-5-methvl-2.2-diphenvlhexanenitrlle Sodium hydride (62mg, 1.55mmol) was added portionwise to an ice-cooled solution of the product of preparation 20 (270mg, 0.775mmol) In dimethylformamide (3ml) under a nitrogen atmosphere. After stirring for 1.5hrs a solution of the product of preparation 32 (380mg,
1.55mmol) in dlmethylformamide (2ml) was added and the mixture was allowed to warm to room temperature and stirred for 18 hours. The solvent was removed In vacua and the residue partitioned between ethyl acetate (10ml) and saturated sodium hydrogen carbonate solution (5ml). The aqueous layer was separated and extracted with further ethyl acetate (10ml). The combined organic layers were washed with water (5ml), brine (5ml), dried over sodium sulphate and concentrated In vacua. The residue was purified by column chromatography on silica gel, eluting with dlchloromethane:methanol:0.88 ammonia (99:1:0.1 to 98:2:0.2 to 95:5:0.5) to afford the title compound as a yellow oil In 38% yield, 150mg. 1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.06(s, 3H), 1.44-1.53(m, 2H), 1.78-1.86(m, 1H), 1.93-2.02(m, 1H), 2.50-2.57(m, 3H), 2.67-2.79(m, 3H), 4.03-4.07(m, 1H), 4.41 (s, 2H), 4.56-4.58(m, 2H), 5.22-5.26(m, 1H), 5.36-5.41(m, 1H), 5.99-6.08(m, 1H), 6.85-6.88(m, 1H), 6.98-7.06(m, 2H), 7,28-7.43(m, 10H); LRMS ESI mfz 513 [M+H]+
Preparation 34
5-[f3R)-3-(4-Fluoro-3-Dropenvloxv-benzvloxvVPvrrolidin-1-yn-5-methvl-2.2-
diphenylhexanamlde
The title compound was prepared from the product of preparation 33, using the same method
as that described for example 2 to afford a colourless oil in 100% yield.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 3H), 1.04(s, 3H), 1.23-1.32(m, 2H), 1.69-1.71 (d, 3H),
1.77-1.86(m, 1H), 189-1.97(m, 1H), 2.40-2.82(m, 6H), 4.02-4.07(m, 1H), 4.39(s, 2H), 4.88-
4.95(m, 1H), 6.37-6.40(m, 1H), 6.95-6.99(m, 1H), 7.04-7.11(m, 2H), 7.22-7.38(m, 10H);
LRMS ESI m/z 531 [M+H]+
Preparation 35
3-Benzvloxv-5-hvdroxv-benzonitrile
Caesium carbonate (2.41 g, 7.4mmol) was added to a solution of 3,5-dihydroxy benzonitrile
(1.0g, 7.4mmol) in dlmethylformamide (5ml) at room temperature and the mixture stirred for
10 minutes. Benzyl bromide (0.880ml, 7.4mmol) was added dropwise and the mixture heated
at 80°C for 30 minutes. The solvent was removed In vacua, the residue treated with water
(10ml), acidified with aqueous hydrochloric acid (2M) and extracted with ethyl acetate (3 x
25ml). The combined organic layers were washed with water (2 x 10ml), brine (10ml), dried
over sodium sulphate and concentrated In vacua. The residue was purified by column
chromatography, eluting with ethyl acetate/pentane (20:80 to 50:50) to afford the title
compound as a white solid in 26% yield, 445mg.
1HNMR(400MHz, CD3OD) 5: 5.07(s, 2H), 6.67-6.70(m, 2H), 6.80(d, 1H), 7.29-7.43(m, 5H);
LRMS ESI m/z 224 [M]'
Preparation 36 5-[(3S)3-f3-Benzvloxv-5-cvano-Phenoxy_-pvrrolldin-1-yl]-5-methvl-2.2-diphenvlhexanamidB
Diisopropyl azodlcarboxylate (215µL, 1.09mmol) was added dropwlse to an ice-cooled solution of triphenyl phosphine (286mg, 1.09mmol), the product from preparation 35 (369mg, 1.64mmol) and the product from preparation 17 (200mg, 0.546mmol) in tetrahydrofuran (10mL), and the mixture was stirred at room temperature for 18 hours. The mixture was concentrated In vacua and purified using an Isolute® SCX-2 cartridge, eluting with methanol, then with 1M ammonia In methanol. Basic fractions were concentrated in vacua and further purified by column chromatography on silica gel, eluting with dichloromethane:methanol: 0.88ammonla (98:2:0.2 to 97:3:0.3) to afford the title compound as an orange foam In 25% yield, 80mg.
1HNMR(400MHz, CD3OD) 5: 0.98(s, 3H), 1.02(s, 3H), 1.20-1.28(m, 3H), 1.81-1.87(m, 1H), 2.07-2.16(m, 1H), 2.34-2.83(m, 5H), 4.74-4.79(m, 1H), 5.10(s, 2H), 6.72-6.74(m, 2H), 6.93(s, 1H), 7.20-7.43(m, 15H); LRMS ESI m/z 574 [M+H]+
Preparation 37
5-((3S)3-r(7-fftert-Butvl(dimethvl)sllyl'|oxy}-2-naphthyl)oxy]pyrrolidJn-1-vl>-5-methvl-2.2-diPhenvlhexanamlde
A solution of 1,1'-Azobis(.NlN'-dimethylformamide) (109mg, 0.630mmol) in.tetrahydrofuran (2ml) was added dropwise to an Ice-cooled solution of triphenyl phosphine (165mg, 0.630mmol), 7-[[dimethyl(1,1-dimethylethyl)silyl]oxy]naphthalen-2-ol [(115mg, 0.420mmol), Journal of Medicinal Chemistry, 1993, Vol. 36, No. 22, p3316] and the product from preparation 17 (171mg, 0.467mmol) In tetrahydrofuran (3mL), and the mixture was stirred at room temperature for 72 hours, then 60°C for 18hrs. The mixture was concentrated in vacua and the residue purified using an Isolute® SCX-2 cartridge, eluting with methanol, then with 0.5M ammonia in methanol. Basic fractions were concentrated in vacua and further purified using a RediSep® silica gel cartridge, eluting with dichloromethane:methanol:0.88 ammonia (100:0:0 to 92:8:0.8) to afford the title compound as a colourless gum in 34% yield, 90mg. 1HNMR(400MHz, CD3OD) 5: 0.25(s, 6H), 0.95-1.10(m, 15H), 1.19-1.33(m, 2H), 1.95(m, 1H), 2.18(m, 1H), 2.34-2.52(m, 2H), 2.56-2.75(m, 2H), 2.76-2.86(m, 1H), 2.87-2.94(m, 1H), 4.90(m, 1H), 6.83-6.96(m, 3H), 7.12(m, 1H), 7.13-7.36(m, 10H), 7.58-7.66(m, 2H); LRMS APCI m/z 623 [M+H]+
Preparation 38
3-Methoxv-4-chloro-benzoic acid allvl ester
Potassium carbonate (4.44g, 32.156mmol) and allyl bromide (2.78ml, 32.156mmol) were added to a stirred solution of 4-chloro-3-methoxybenzoic acid (3g, 16.078mmol) in N,N-dimethylformamide (30ml) and allowed to stir at room temperature for 18 hours. The reaction mixture was partitioned between diethyl ether (200ml) and water (150ml), the organic phase extracted and further washed with water (150ml), dried over sodium sulfate and concentrated in vacua to afford the title compound as an orange oil in 98% yield, 3.57g.
1HNMR(400MHz, CD3OD) 5: 3.92(s, 3H), 4.79-4.82(d,2H), 5.26-5.29(d,1H), 5.37-5.42(d, 1H), 6.00-6.1 0(m, 1H), 7.44-7.46(d, 1H), 7.56-7.59(dd, 1H), 7.62-7.63(d, 1H); LRMS ESI m/Z 227
Preparation 39
3-Hvdroxy-4-chloro-benzolc acid
Boron tribromlde (1 M In dichioromethane, 31 ml, 31 .504mmol) was added to an ice-cooled solution of the product of preparation 38 (3.56g, 15.752mmol) In dichioromethane (30mL) and the mixture was stirred at 0°C to room temperature for 18 hours. The reaction was quenched with 0.88 ammonia solution and stirred at room temperature for 90 minutes. The reaction mixture was acidified to pH 1 by dropwise addition of 2N hydrochloric acid (aq) and extracted with diethyl ether (2x50mL). The combined organic layers were dried over sodium sulfate and concentrated In vacua to afford the title compound as a pale yellow solid in 90% yield, 2.45g. 1HNMR(400MHz, CD3OD) 5: 7.36-7.38(d, 1H), 7.44-7.47(dd, 1H), 7.54-7.55(d, 1H); LRMS APCI m/z 171 [M-H]
Preparation 40
3-Allyloxy-4-chloro-benzolc acid allvl ester
Potassium carbonate (4.9g, 35.057mmol) and ally! bromide (3.07ml, 35.507mmol) were added to a stirred solution of the product of preparation 39 (2.45g, 14.203mmol) in N,N-dimethylformamide (30ml) and allowed to stir at room temperature for 18 hours. The reaction mixture was partitioned between diethyl ether (70ml) and water (70ml), the organic phase was then extracted and further washed with water (50ml), dried over sodium sulfate and concentrated in vacua. The residue was purified by column chromatography on silica gel, eluting with pentane-.ethyl acetate, 100:0 to 90:10, to afford the title compound as a pale orange oil in 74% yield, 2.65g.
1HNMR(400MHz, CD3OD) 5: 4.66-4.68(d, 2H), 4.79-4.81 (d, 2H), 5.25-5. 31 (t,2H), 5.36-5.49(q, 2H), 6.00-6.12(m, 2H), 7.45-7.47(d, 1H), 7.56-7.59(dd, 1H), 7.62(d, 1H)
Preparation 41
(3-Allvloxy-4-chloro-phenvn-methanol
A solution of the product of preparation 40 (2.6g, 10.30mmol) in tetrahydrofuran (40ml) was added dropwise to a stirred solution of lithium aluminium hydride (1M in tetrahydrofuran, 21ml, 20.60mmol) over 30 minutes at room temperature and allowed to stir for 18 hours. The reaction mixture was quenched by dropwise addition of water (1ml), 2M sodium hydroxide (2ml) and water (3ml) and allowed to stir for 3 hours. The mixture was then filtered, washing with diethyl ether (2x20ml) and water (10ml). The organic phase was extracted, dried over sodium sulfate and concentrated in vacua to afford the title compound as a colourless oil in 69% yield, 1.4g.
'HNMR^OOMHz, CD3OD) 5: 4.50(s, 2H), 4.60-4.62(d, 2H), 5.24-5.28(d, 1H), 5.42-5.48(d, 1H), 6.03-6.12(m, 1H), 6.87-6.90(d, 1H), 7.05(s, 1H), 7.29-7.31(d, 1H); LRMS ESI m/z 198 [M+H]+
Preparation 42
2-Allvloxv-4-bromomethvl-1-chlorobenzene
Dibromotriphenylphosphorane (3.27g, 7.75Bmmol) was added to a stirred solution of the product of preparation 41 (1.4g, 7.053mmol) In acetonitrile (50ml) and allowed to stir at room temperature for 18 hours. Further dibromotriphenylphosphorane (3.27g, 7.758mmol) was added and the reaction mixture stirred at room temperature for a further 6 hours. The solution was then concentrated In vacua and recrystallised from hot ethyl acetate (25ml) and diethyl ether (25ml). The solid was filtered from solution and the filtrate concentrated In vacua. The residue was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 100:0 to 80:20, to afford the title compound as a colourless oil in 48% yield, 890mg. 1HNMR(400MHz, CD3OD) 5: 4.52(s, 2H), 4.61-4.63(d, 2H), 5.25-5.29(d, 1H), 5.42-5.48(d, 1H), 6.02-6.11(m, 1H), 6.95-6.98(d, 1H), 7.10(d, 1H), 7.30-7.32(d, 1H)
Preparation 43
5-[(3R)-3-(3-Allvloxv-4-chloro-benzvloxy)-pvrrolld!n-1-yl]-5-methvl-2.2-diphenvlhexanenitrile A solution of the product of preparation 20 (180mg, 0.515mmol) in N,N-dimethylformamlde (3ml) was added to an Ice-cooled solution of sodium hydride (60% dispersion In mineral oil, 41 mg, 1.032mmol) in N,N-dlmethylformamide (2mL) and the mixture was stirred at 0°C for 30 minutes. The product of preparation 42 (270mg, 1.032mmol) was added and the mixture was stirred for 18 hours at 0°C to room temperature. The reaction was ice-cooled, further sodium hydride (41 mg, 1.032mmol) was added and the mixture was stirred for a further 3 hours at room temperature. The reaction mixture was then quenched with water (3mL), concentrated In vacua and the aqueous residue was partitioned between ethyl acetate (30mL) and water (20mL). The organic layer was separated and washed with water (2x20mL), then concentrated in vacua. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, to afford the title compound as a brown gum In 62% yield, 170mg.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 3H), 1.05(s, 3H), 1.43-1.52(m, 2H), 1.78-1.86(m, 1H), 1.93-2.02(m, 1H), 2.49-2.56(m, 3H), 2.65-2.79(m, 3H), 4.03-4.08(m, 1H), 4.43(s, 2H), 4.56-4.58(d, 2H), 5.22-5.26(d, 1H), 5.39-5.45(d, 1H), 5.99-6.08(m, 1H), 6.85-6.88(dd, 1H), 7.01-7.02(d, 1H), 7.26-7.42(m, 11H); LRMS APCI m/z 529 [M+H]+
Preparation 44
5-[(3R)-3-(4-Chloro-3-propenvloxv-benzvloxy)-pvrrolldin-1-yl]-6-methvl-2.2-
diphenvlhexanamide
Potassium hydroxide (340mg, 6,055mmol) was added to a solution of the product of preparation 43 (160mg, 0.303mmol) in 3-methyl-3-pentanol (7mL) and the mixture was heated under reflux for 24 hours. The reaction mixture was then cooled to room temperature, concentrated In vacua and the residue was partitioned between ethyl acetate (25mL) and water (25mL). The aqueous layer was separated, extracted with further ethyl acetate (25mL) and the combined organic layers were dried over sodium sulfate and concentrated In vacua to afford the title compound as a yellow gum in 97% yield, 161mg.
1HNMR(400MHz, CD3OD) 8: 0.97(s, 3H), 0.99(s, 3H), 1.21-1.27(m, 2H),1.70-1.72(d, 3H), 1.74-1.80(m, 1H), 1.87-1.93(m, 1H), 2.39-2.44(m, 2H), 2.45-2.50(m, 1H), 2.53-2.57(dd, 1H), 2.59-2.65(q, 1H), 2.68-2.72(m, 1H), 3.98-4.02(m, 1H), 4.39(s, 2H), 4.93-5.00(m, 1H), 6.38-6.40(m, 1H), 6.94-6.97(dd, 1H), 7.04(d, 1H), 7.20-7.39(m, 11H); LRMS APCI m/z 547 [M+H]+
Preparation 45
5-[(3R)-3-(3-benzvloxv-4-cvanQ-phenoxv)Dvrrolidln-1-yl]-5-methvl-2.2-dlphenvlhexanamlde Sodium hydride (60% dispersion in mineral oil, 26mg', 0.656mmol) was added to an Ice-cooled solution of the product of preparation 17. (200mg, 0.546mmol) in N,N-dimethylformatnide (5mL) and the mixture was stirred for 60 minutes. 2-Benzyloxy-4-fluoro-benzonitrile (136mg, 0.601 mmol) was added and the mixture was stirred for 18 hours at room temperature. The reaction mixture was quenched with water (3mL), concentrated in vacua and the aqueous residue was partitioned between ethyl acetate (20mL) and water (15mL). The aqueous layer was separated and extracted with further ethyl acetate (2x10mL). The combined organic layers were concentrated In vacua and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88ammonia, 95:5:0.5, to afford the title compound as a white foam in 33% yield, 105mg.
1HNMR(400MHz, CD3OD.) 6: 0.95(s, 3H), 1.02(s, 3H), 1.19-1.25(m, 2H), 1.79-1.88(m, 1H), 2.07-2.16(m, 1H), 2.33-2.49(m, 2H), 2.51-2.58(m, 2H), 2.67-2.74(m, 1H), 2.79-2.83(m, 1H), 4.80-4.84(m, 1H), 5.20(s, 2H), 6.49-6.52(dd, 1H), 6.57-6.58(d, 1H), 7.20-7.38(m, 13H), 7.44-7.46(m, 2H), 7.48-7.50(d, 1 H); LRMS APCI m/z 574 [M+H]+
Preparation 46
(3-Allvloxy-2-chloro-phenvn-methanol
Sodium borohydride (185mg, 4.883mmol) was added to a solution of the product of preparation 99 (SOOmg, 4.07mmol) in ethanol (30ml) and the mixture stirred at room temperature for 18 hours. The mixture was quenched by addition of water (30ml) followed by dropwise addition of glacial acetic acid until effervescence ceased. The mixture was then extracted with diethyl ether (2 x 50ml) and the combined organic layers were washed with saturated aqueous sodium hydrogen carbonate solution (40ml), dried over sodium sulfate and concentrated In vacua to afford the title compound as a colourless gum in 100% yield, 805mg.
1HNMR(400MHz, CD3OD) 5: 4.60-4,62(m, 2H), 4.66-4.69(d, 2H), 5.24-5.28(d, 1H), 5.43-5.47(d, 1H), 6.0l-6.12(m, 1H), 6.82-6.84(d, 1H), 7.09-7.12(m, 1H), 7.22-7.26(m, 1H); LRMS ESI m/z 198 [M+H]+
Preparation 47
3-Allyloxv-2-chloro-benzvl bromide
Dibromotrlphenylphosphorane (1.87g, 4.431 mmol) was added to a solution of the product of preparation 46 (SOOmg, 4.028mmol) in acetonitrile (30ml) and the mixture allowed to stir at room temperature for 18 hours. Additional dibromotriphenylphosphorane (1.87g, 4.431mmol) was added and the mixture stirred at room temperature for a further 6 hours. The solution was concentrated in vacua and the residue recrystallised from hot ethyl acetate (15ml) and diethyl ether (15ml). The solid was filtered from solution and the filtrate concentrated in vacua. The residue was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 100:0 to 90:10, to afford the title compound as a colourless oil in 27% yield, 285mg. 1HNMR(400MHz, CD3OD) 5: 4.61-4.63(m, 2H), 4,65(s, 2H), 5.26-5.29(d, 1H), 5.43-5.49(d, 1H), 6.00-6.11(m, 1H), 7.01-7.03(d, 1H), 7.08-7.10(d, 1H), 7.20-7.24(1, 1H); LRMS APCl m/z 262 [M+H]+
Preparation 48
5-[(3RV3-(3-Allvloxv-2-chloro-benzvloxv)-Pvrrolldin-1-vl1-5-methvl-2.2-diphenvlhexanenitrile The title compound was prepared from the product of preparation 47 and the product of preparation 20, using the same method as that described for preparation 43, to afford a brown gum in 46% yield.
1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.06(8, 3H), 1.45-l'.51(m, 2H), 1.81-1.90(m, 1H), 1.95-2.04(m, 1H), 2.50-2.58(m, 3H), 2.65-2.79(m, 3H), 4.07-4.12(m, 1H), 4.49-4.54(m, 2H), 4.59-4.61(m, 2H), 5.24-5.27(d, 1H), 5.41-5.47(d, 1H), 6.02-6.11(m, 1H), 6.96-6.98(d, 1H), 7.06-7.08(d, 1H), 7.17-7.42(m, 11H); LRMS APCl m/z 529 [M+H]+
Preparation 49
5-[(3RV3-(2-Chloro-3-Dropenvloxv-benzvloxv)-Dvrrolldin-1-yl]-5-methvl-2.2-
diphenvlhexanamide
The title compound was prepared from the product of preparation 48, using the same method
as that described for preparation 44, to afford a yellow gum in 100% yield.
1HNMR(400MHz, CD3OD) 5: 0.98(s, 3H), 1.01(s, 3H), 1.23-1.27(m, 2H), 1.71-1.73(d, 3H),
1.78-1.85(m, 1H), 1.90-1.97(m, 1H), 2.40-2.44(m, 2H), 2.46-2.58(m, 2H), 2.61-2.67(q, 1H),
2.71-2.75(m, 1H), 4.03-4.09(m, 1H), 4.52-4.53(d, 2H), 4.93-5.00(m, 1H), 6.40-6.42(m, 1H),
7.00-7.02(d, 1H), 7.11-7.40(m, 12H); LRMS APCl m/z 547 [M+H]+
Preparation 50 5-Oxo-S-(4-phenoxvplperidin-1-yl)-2.2-dlphenylpentanenitrile
1-Hydroxybenzotriazole hydrate (5.67g, 42mmol) and triethytamine (14.88mL, 107mmol) were added to 4-cyano-4,4-diphenylbutanoic acid (W097/24325) (10.39g, 39mmol) and 4-phenoxy-piperidine hydrochloride (6.32g, 36mmol) in .N.N-dimethylformamlde (150mL). The mixture was stirred for 10 minutes. 1-(3-Dlmethylamlnopropyl)-3-ethylcarbodiimlde hydrochloride (8.20g, 42mmol) was then added and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated in vacuo and the residue was partitioned between ethyl acetate (100mL) and water (100mL). The organic layer was separated, washed with water (100mL) and brine (30mL), dried over magnesium sulfate and concentrated in vacuo. The residue was triturated with diethyl ether, filtered off, washed through with diethyl ether and purified by column chromatography on silica gel, eluting with pentaneiethyl acetate, 75:25 to 50:50, to afford the title compound as a white solid (14.4g) in a 95% yield.
1HNMR(400MHz, CDCI3) 5: 1.74-1.90(m, 4H), 2.45-2.49(m, 2H), 2.79-2.83(m, 2H), 3.27-3.33(m, 1H), 3.54-3.61 (m, 1H), 3.62-3.74(m, 2H), 4.49-4.53(m, 1H), 6.87-6.91 (m, 2H), 6.93-6.98(m, 1H), 7.26-7.43(m, 12H); LRMS APCI m/z426 [M+H]+
Preparation 51'
tert-Butyl4-r(3-bromobenzvnoxvlpiperidine-1-carboxvlate
Sodium hydride (60% dispersion in mineral oil, 3.31 g, 83mmol) was added to an ice-cooled solution of 1-tert-butoxycarbonyl-4-hydroxy-piperidine (16.64g, 83mmol) in tetrahydrofuran (200mL) and the mixture was stirred at 0°C for 30 minutes. 3-Bromobenzyl bromide (20.66g, 83mmol) was added and the mixture was stirred at room temperature for 18 hours. The reaction was then quenched with water (50ml) and concentrated in vacuo. The aqueous residue was extracted with ethyl acetate (2x100ml) and the combined organic phases were washed with brine (100ml), dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethyl acetate, 90:10 to 80:20, to afford the title compound as a colourless oil in 61% yield, 18.64g. 1HNMR(400MHz, CDCI3) 5: 1.45(s, 9H), 1.54-1.62(m, 2H), 1.81-1.88(m, 2H), 3.08-3.14(m, 2H), 3.52-3.58(m, 1H), 3.73-3.79(m, 2H), 4.51 (s, 2H), 7.18-7.26(m, 2H), 7.38-7.41 (m, 1H), 7.49(m, 1H); LRMS APCI m/z 372 [M+H]+
Preparation 52
4-[(3-Bromobenzvnoxv]plperidlne
Hydrochloric acid (4M In dioxan, 340ml) was added to a solution of the product of preparation 51 (18.64g, SOmmol) in dioxan (50ml) and the mixture was stirred at room temperature for 2.5 hours. The reaction mixture was concentrated In vacuo and the residue was dissolved in 2M aqueous hydrochloric acid (200mL) and washed with diethyl ether (2x100mL). The aqueous layer was adjusted to pH10 with 2M aqueous sodium hydroxide solution, extracted with diethyl ether (3x200mL). The combined organic phases were dried over sodium sulfate
and concentrated in vacuo -to afford the title compound as a colourless oil in 98% yield,
13.39g.
1HNMR(400MHz, CDCI3) 6: 1.45-1.55(m, 2H), 1.92-1.97(m, 2H), 2.58-2.64(m, 2H), 3.07-
3.13(m, 2H), 3.42-3.49(m, 1H), 4.51(s, 2H), 7.17-7.27(m, 2H), 7.37-7.40(m, 1H), 7.50(m, 1H);
LRMS APCI m/z 270 [M+H]+
• i
Preparation 53
5-f4-r(3-Bromobenzvnoxvlp|perldin-1-yll-S-oxo-2.2-diphenylpentanenitrile
The title compound was prepared from 4-cyano-4,4-diphenylbutanoic acid (W09724325) and
the product of preparation 52 using the same method as that described for preparation 50, in
95% yield.
1HNMR(400MHz, CDCI3) 5:1.63{m, 2H), 1.82(m, 2H), 2.46(m, 2H), 2.80(m, 2H), 3.17(m, 1H),
3.35(m, 1H), 3.51-3.64(m, 2H), 3.88(m, 1H), 4.44-4.53(m, 2H), 7.17-7.42(m, .14H); LRMS
APCI m/z 519 [M+H]+
Preparation 54
S-{4-Hvdroxv-plperidln-1 •vl)-5-methyl-2,2-dlphenvl-hexanoic acid amide
A 1M HCI aqueous solution (9.43mL, 9.43mmol) was added to a stirred solution of example
91 in ethanol (250ml). 20% Palladium (II) hydroxide on carbon (1g) was added and the
resulting mixture stirred under an atmosphere of hydrogen gas (50psi) at 50°C for 18 hours.
The reaction mixture was filtered through arbocel and then concentrated In vacuo. The
residue was dissolved in water (100mL), the solution adjusted to pH 12 with 2M aqueous
sodium hydroxide solution and extracted with ethyl acetate (3x100mL). The combined organic
layers were dried over magnesium sulfate and concentrated in vacuo to yield a white foam in
95% yield, 3.39g.
1HNMR(400MHz, CD3OD) 6: 0.97(s, 6H), 1.23-1.27(m, 2H), 1.39-1.48(m, 2H), 1.74-1.78(m,
2H), 2.06-2.11 (m, 2H), 2.40-2.44(m, 2H), 2.65-2.68(m, 2H), 3.47(m, 1H), 7.23-7.39(m, 10H);
LRMS ESI m/z 381 [M+H]+
Preparation 55
5-Amino-5-methyl-2.2-diphenvlhexanenitrile
Potassium tert-butoxide'(203mg, 1.81mmol) and tert-butyl 4,4-dlmethyl-1l2,3-oxathlazinane-3-carboxylate 2,2-dioxide [(400mg, 1.51mmol), W02003037327, p83] were added to a solution of diphenylacetonitrile (349mg, 1.81mmol) in N,N-dimethyiformamide (5mL) and the mixture was stirred for 18 hours at room temperature. The reaction mixture was then concentrated in vacuo and the residue was treated with hydrochloric acid (4M in dioxane, 10mL) and heated at40°C for 2.5 hours. The reaction mixture was concentrated In vacuo and the residue was basified with saturated sodium hydrogen carbonate solution and extracted with ethyl acetate (2x30mL). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on
silica gel, eluting with dichloromethane:methanoi:0.88 ammonia, 90:10:1, to afford the title compound as a colourless oil in 77% yield, 324mg.
1HNMR(400MHz, CDCI3) 6: 1.17(m, 6H), 1.48-1.57(m, 2H), 2.20-2.40(brs, 2H), 2.42-2.53(m, 2H), 7.22-7.43(m, 10H); LRMS APCI m/z 279 [M+H]+
Preparation 56
5-(3-Hvdroxvazetldin-1-yl)-S-methvl-2.2-dlphenvlhexanenitriie
A mixture of (+/-)-epichlorohydrin (1.47mL, 18.76mmol) and the product of preparation 55 (4.74g, 17mmol) in methanol (50mL) was heated at 60°C for 48 hours. The reaction mixture was then concentrated in vacuo and the residue was partitioned between ethyl acetate (50mL) and sodium hydrogen carbonate solution (30mL). The aqueous layer was separated and extracted with ethyl acetate (2x50mL). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 95:5:0.5, to afford the title compound as a pale yellow oil in 50%.yield, 2.86g. 1HNMR(400MHz, CDCI3) 5: 0.93(s, 6H), 1.29-1.39(m, 2H), 2.38-2.50(m, 2H), 2.90-3.00(m, 2H), 3.29-3.39(rh, 2H), 4.29-4.39(m, 1H), 7.24-7.45(m, 10H); LRMS APCI m/z 335 [M+H]+
Preparation 57
1-(4-Cvano-1.1 -dimethvl-4.4-diphenylbutyl^azetldin-3-vl methanesulfonate
Methane sulfonyl chloride (3.3mL, 43mmol) was added to a solution of the product of
preparation 56 (4.82g, 14.4mmol) in pyridine (50mL) cooled to -15°C. The mixture was stirred
for 2 hours, allowing the temperature to warm to 0°C, then concentrated in vacuo. The residue
was partitioned between ethyl acetate (100mL) and sodium hydrogen carbonate solution
(100mL) and the organic layer was separated, dried over magnesium sulfate and
concentrated in vacuo. Purification of the residue by column chromatography on silica gel,
eluting with pentane:ethylacetate/methanol/0.88 ammonia (90/10/1) 2:1, afforded the title
compound as a yellow oil in 81% yield, 4.80g.
1HNMR(400MHz, CDCI3) 5: 0.95(s, 6H), 1.30-1.41(m, 2H), 2.42-2.55(m, 2H), 2.98(s, 3H).
3.25-3.37(m, 2H), 3.44-3.56(m, 2H), 5.00-5.06(m, 1H), 7.23-7.44(m, 10H); LRMS APCI m/z
413 [M+H]+
Preparation 58
Azetldln-3-yl methanesulfonate hvdrochloride
A mixture of 1-(diphenylmethyl)azetidin-3-yl methanesulfonate (WO9725322, p64), (20g,
63mmol) and chloroethylchloroformate (10mL, 95mmol) in dichloromethane (100mL) was
heated under reflux for 2.5 hours. The reaction mixture was then concentrated in vacuo and
the residue was re-dissolved in methanol (100mL) and heated under reflux for a further 2.5
hours. The mixture was then cooled to room temperature and concentrated in vacuo to afford
the title compound as a white solid in quantitative yield, 9.6g.
1HNMR(400MHz, DMSO-d8) 5: 3.28(s, 3H), 4.00-4.15(m, 2H), 4.31(m, 2H), 5.28-5.38(m, 1H); LRMS APCI m/z 152 [M+H]+
Preparation 59
4-Cvano-4.4-diphenvlbutanovl chloride
N,N-Dimethylformamide (1 drop) was added to a suspension of 4-cyano-4,4-dlphenylbutanoic acid [(7.8g, 29mmol), W097/24325] and oxalyl chloride (5.2mL, 60mmol) in dichloromethane (40mL) and the mixture was stirred at room temperature for 2 hours. The reaction mixture was then concentrated in vacuo and the residue was azeotroped with toluene (3x50mL) to afford the crude title compound. The material was used in preparation 60 without further purification.
Preparation 60
1 -(4-Cvano-4.4-diphenylbutanovnazejldln-3-vl methanesulfonate
Triethylamine (12.3mL, 87mmol) and a solution of the product of preparation 59 (8.23g,
29mmol) In dichloromethane were added dropwise to a solution of preparation 58 ,(5.53g,
29mmol) In dichloromethane (50mL), cooled to -78°C, and the mixture was stirred at this
temperature for 1 hour. The reaction mixture was quenched with 2N hydrochloric acid (50mL)
and the organic layer was separated, dried over magnesium sulfate and concentrated in
vacuo . Purification of the residue by column chromatography on silica gel, eluting with ethyl
acetaterpentane, 50:50 to 100:0, afforded the title compound as a yellow oil in 97% yield,
11.4g.
1HNMR(400MHz, CDCI3) 5: 2.17-2.29(m, 2H), 2.71-2.80(m, 2H), 3.05(s, 3H), 4.03-4.20(m,
2H), 4.26-4.38(m, 2H), 5.18-5.22(m, 1H), 7.24-7.45(m, 10H); LRMS APCI m/z 399 [M+H]+
Preparation 61
5-(3-[2-(Benzvloxvlphenoxy1azetidln-1-vll}-5-oxo-2.2-diphenvlDentanenitrile
The title compound was prepared from the product of .preparation 60 and 2-
(benzyloxy)phenol, using the same method as that described for example 99, as a yellow oil
in 77% yield.
1HNMR(400MHz, CDCI3) 8: 2.18-2.24(m, 2H), 2.75-2.80(m, 2H), 4.02-4.10(m, 2H), 4.23-
4.33(m, 2H), 4.82-4.91 (m, 1H), 5.08(s, 2H), 6.62-6.65(m, 1H), 6.84-6.99(m, 3H), 7.24-7.43(m,
15H); LRMS APCI m/z 503 [M+H]+
Preparation 62
5-{3-[2-(Benzyloxv)phenoxy1azetidln-1-yl}-5-methvl-2.2-diphenvlhexanenitrlle
A solution of the product of preparation 61 (700mg, 1.39mmol) in tetrahydrofuran (10mL) was
cooled to -35°C. Zirconium chloride (650g, 2.78mmo!) was added and the reaction mixture
was stirred at -35°C for 1 hour. Methyl magnesium chloride (3M in tetrahydrofuran, 4.2mL,
12.6mmol) was then added dropwise and the mixture was stirred for 3 hours, with the
temperature maintained below -20°C. The reaction was quenched with 1N sodium hydroxide solution (10mL) and the mixture was filtered through Arbocel®, washing through with ethyl acetate. The organic layer of the filtrate was separated, washed with brine (20mL), dried over magnesium sulfate and concentrated In vacuo. Purification of the residue by 'column chromatography on silica gel, eluting with pentane:ethyl acetate, 85:15 to 50:50 afforded the title compound as a yellow oil in 10% yield, 69mg.
1HNMR(400MHz, CDCI3) 6: 0.98(s, 6H), 1.35-1.42(m, 2H), 2.45-2.58(m, 2H), 3.20-3.32(m, 2H), 3.40-3.55(m, 2H), 4.68-4.78(m, 1H), 5.13(s, 2H), 6.64-6.72(d, 1H), 6.85-6.99(m, 3H), 7.24-7.48(m, 15H); LRMS ESI m/z 517 [M+H]+
Preparation 63
S-(3.f2-(Benzvloxv^Phenoxvlazetldin-1-yl]-5-methvl-2,2-diphenvlhexanamlde
The title compound was prepared from the product of preparation 62, using the same method
as that described for example 100, as a colourless gum in 55% yield.
1HNMR(400MHz, CDCI3) 5: 0.90(s, 6H), 1.15-1.22(m, 2H), 2.42-2.52(m, 2H), 3.18-3.32(m,
2H), 3.40-3.58(m, 2H), 4.65-4.78(m, 1H), 5.13(s, 2H), 5.40-5.60 (m, 2H), 6.62:6.70(m, 1H),
6.82-6.97(m, 3H), 7.23-7.44(m, 15H); LRMS APCI m/z 535 [M+H]+
Preparation 64
3-Phenoxvazetidlne hvdrochloride
10% Pd/C (2.5g) was added to a solution of 1-(diphenylmethyl)-3-phenoxy-azetid!ne (27 7g, 88mmol) in ethanol (100mL) and acetic acid (100mL) and the mixture was stirred at room temperature, under SOpsi of hydrogen, for 24 hours. The reaction mixture was then filtered through Arbocel® and the filtrate was concentrated in vacuo. The residue was dissolved in diethyl ether (200mL), cooled to 0°C and treated with hydrochloric acid (1M in diethyl ether, 120ml). The solvent was then evaporated under reduced pressure and the residue was azeotroped with toluene and triturated with ethyl acetate to afford the title compound as a white solid in 86% yield, 13.99g. LRMS APCI m/z 160 [M+H]+
Preparation 65
5-Oxo-5-(3-phenoxvazetidin-1-vl)-2.2-diPhenvlpentanenitrile
A mixture of the product of preparation 64 (1.13g, 7.6mmol), 4-cyano-4,4-diphenylbutanoic acid [(2.4g, 9.12mmol), W097/24325], 1-(3-dimethylaminopropyl)-3-ethylcarbodllmide hydrochloride (1.76g, 9.12mmol), 1-hydroxybenzotriazole hydrate (1.30g, 9.12mmol) and N.N-dilsopropylethylamine (5.3ml, 19mmol) in dlchloromethane (50mL) was stirred at room temperature for 18 hours. The reaction mixture was then diluted with ethyl acetate (50ml), washed with 2M hydrochloric acid (30ml), and sodium hydrogen carbonate solution (30ml), dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by
column chromatography on silica gel, eluting with pentane:ethyl acetate, 100:0 to 0:100, then afforded the title compound as a colourless oil in 75% yield, 2.28g.
1HNMR(400MHz, CDCI3) 6: 2.20-2.25(m, 2H), 2.75-2.82(m, 2H), 3.97-4.08(m, 2H), 4.28-4.40(m, 2H), 4,85-4.90(m, 1H), 6.65-6.74(m, 2H), 6.98-7.04(m, 1H), 7.24-7.43(m, 12H); LRMS APC) m/z 397 [M+H]+
Preparation 66
tert-ButvP-flodomethvnphenoxvldimethvlsllane
TriphenyJ phosphine (1.32g, 5.03mmol), imidazole (370mg, 5.47mmol) and iodine (1.16g,
4.61 mmol) were added to an Ice-cooled solution of 4-(tert-butyldimethylsilyloxy)benzyl alcohol
[(1g, 4.19mmol), Tet. Lett. (2004), 45, 9617] in tetrahydrofuran (50mL) and the mixture was
stirred at 0°C for 10 minutes and room temperature for 30 minutes. The reaction mixture was
then concentrated in vacuo and the residue was partitioned between ethyl acetate and water.
The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo.
Purification of the residue by column chromatography on silica gel, eluting with pentane,
afforded the title compound in 41 % yield, 600mg.
1HNMR(400MHz, CDCI3) 6: 0.00 (s, 6H), 0.78 (s, 9H), 4.26 (s, 2H), 6.72-6.98 (m, 2H), 7.22-
7.28 (m, 2H)
Preparation 67
5-Allvioxy-2.4-dichloro-phenol
4,6-dichlororesorcinol (3.80g, 21 mmol), aliyl bromide (1.82mL, 21 mmol) and potassium
carbonate (2.24g, 21 mmol) were combined in DMF and stirred at room temperature for 18
hours. The DMF was removed in vacuo and the residue acidified with 2M hydrochloric acid
(50mL)' and extracted with ethyl acetate (2x50mL). The combined organic solution was dried
over magnesium sulphate and concentrated in vacuo. The residue was purified by column
chromatography on silica gel, eluting with pentane:ethyl acetate 9:1 to 4:1 to afford the title
compound as a yellow oil in 27% yield, 1.24g.
1HNMR(400MHz, CDCI3) 5: 4.55-4.60 (m, 2H), 5.33-5.52 (m, 2H), 5.95-6.10 (m, 1H), 6.62 (s,
1H), 7.3 (s, 1H); LRMS ESI m/z 217 [M-H]
Preparation 68
5-[3-(5-Allvloxv-2,4-dlchloro-phenoxy)-azetldin-1-yl]-5-methvl-2,2-diphenvl-hexanenitrlle The title compound was prepared from the products of preparation 67 and preparation 57, using the same method as that described for example 99, as a colourless gum in 93% yield. 1HNMR(400MHz, CDCI3) 5: 0.98 (s, 6H), 1.31-1.40 (m, 2H), 2.41-2.55 (m, 2H), 3.20-3.25 (m, 2H), 3.48-3.58 (m, 2H), 4.55-4.58 (m, 2H), 4.62-4.75 (m, 1H), 5.32-5.38 (m, 1H), 5.40-5.48 (m, 1H), 5.95-6.10 (m, 1H), 6.28 (s, 1H), 7-25-7.45 (m, 11H); LRMS APCI m/z 535 [M+H]+
Preparation 69
2-Allvloxv-4,5-dichloro-phenol
The title compound was prepared from 4,5-dlchlorocatechol using the same method as that
described for preparation 67, as a pink solid In 62% yield.
1HNMR(400MHz, CDCI3) δ: 4.55-4.60 (m, 2H), 5.35-5.46 (m, 2H), 5.81 (1H, S), 5.95-6.10 (m,
1H), 6.90 (s, 1H), 7.03 (s, 1H); LRMS APCI m/z 217 [M-H]
Preparation 70
S-f3-(2-Allvloxv-4.5-dichloro-phenoxy)-azetldin-1-yl]-5-methvl-2.2-diphenvl-hexanenitrile The title compound was prepared from the products of preparation 69 and preparation 57, using the same method as that described for example 99, as a colourless gum in 75% yield. 1HNMR(400MHz, CDCI3) B: 0.98 (s, 6H), 1.31-1.40 (m, 2H), 2.41-2.55 (m, 2H), 3.15-3.25 (m, 2H), 3.36-3.50 (m, 2H), 4.50-4.58 (m, 2H), 4.60-4.66 (m, 1H), 5.28-5.42 (m, 2H), 5.95-6.10 (m, 1H), 6.65 (s, 1H), 6.95 (s, 1H), 7-25-7.45 (m, 10H); LRMS APCI m/z 535 [M+H]+
Preparation 71
1-Allvloxy-3-bromomethyl-benzene
To a solution of (3-allyloxy-phenyl)-methanol (Tetrahedron (2000), 56(13), 1873-1882)
(1.07g, 6.49mmol) in THF (7mis) at 3°C was added carbon tetrabromide (2.69g, 8.11mmol)
then trlphenylphosphine (2.13g, 8.11mmol) in THF (2mls). The reaction mixture was stirred at
5°C for 1 hour. The reaction mixture was filtered and concentrated in vacuo. The residue was
washed with pentane to give a yellow solid which was purified by column chromatography on
silica gel, eluting with pentaneiethyl acetate, 100:0, to 95:5 to afford the title compound as a
pale yellow oil in 24% yield, 350mg.
1HNMR(400MHz, CDCIg) 6: 4.47 (s, 2H), 4.51-4.60 (m, 2H), 5.26-5.35 (m, 1H), 5.37-5.47 (m,
1H), 5.99-6.11 (m, 1H), 6.82-6.90 (m, 1H), 6.92-7.01 (m, 2H), 7.21-7.30 (m, 1H).
Preparation 72
S-[3-(3-Allvloxy-benzyloxy)-azetidin-1-yl]-5-methvl-2.2-dlphenvl-hexanenltrlle Sodium hydride (60% dispersion in mineral oil) 24mg, 0.596mmol) was added portionwise to an ice-cooled solution of the product of preparation 56 (166mg, 0.496mmoi) in N,N-dimethylformamide (2mL) and the mixture was stirred at 0°C for 15 mins. The product of preparation 71 (169mg, 0.746mmol) was added and the mixture was stirred for 0.5 hour at 0°C. The reaction mixture was then quenched with 2N hydrochloric acid (2mL) then basified with saturated sodium hydrogen carbonate solution. The resulting mixture was then partitioned between ethyl acetate (50mL) and water (10mL). The aqueous layer was separated and extracted with ethyl acetate (1x50mL). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 98:2:0.2 to afford the title compound as a colourless gum in 54% yield, 130mg.
1HNMR(400MHZ, CDCI3) 6: 0.93(s, 6H), 1.26-1.38 (m, 2H), 2.38-2.50 (m, 2H), 2.96-3.10 (m, 2H), 3.18-3.36 (m, 2H), 4.06-4.18 (m, 1H), 4.39 (s, 2H), 4.52-4.58 (m, 2H), 5.25-5.33 (m, 1H), 5.37-5.47 (m, 1H), 8.00-6.11 (m, 1H), 6.81-6.93(m, 3H), 7.20-7.45(m, 11H); LRMS APCI m/z 481 [M+H]+
Preparation 73
5-Methvl-2.2-dlphenvl-5-[3-((3-proDenvloxv-benzvloxy)-azetldin-1-yl]-hexanolcacid amide Potassium hydroxide (303mg, 5.42mmol) was added to a solution of preparation 72 (130mg, 0.271 mmol) in 3-methyl-3-pentanol (5mL) and the mixture was heated under reflux for 24 hours. The reaction mixture was then cooled to room temperature, concentrated in vacub and the residue was partitioned between ethyl acetate (50mL) and water (10mL). The aqueous layer was separated, extracted with ethyl acetate (2x30mL) and the combined organic solution was dried over magnesium sulfate and concentrated In vacuo to give a colourless gum in 96% yield, 130mg.
1HNMR(400MHz, CDCI3) 6; 0.87(s, 6H), 1.07-1.19(m, 2H), 1.64-1.76 (m, 3H), 2.37-2.47(m, 2H), 2.94-3.10 (m, 2H), 3.20-3.40(m, 2H), 4.08-4.20(m, 1H), 4.35 (s, 2H), 4.83-4.93(m, 1H), 5.35-5.65 (d, 2H), 6.34-6.40 (d, 1H), 6.88-6.98(m, 3H), 7.20-7.40 (m, 11H); LRMS APCI m/z 499[M+H]+
Preparation 74
3-Allvloxy-2.6-dlchloro-ben2aldehvde
2,6-dichloro-3-hydroxybenzaldehyde (960mg, 5.03mmol) (Synthesis, 2004, 12, 2062), allyl bromide (431 (iL, 5.03mmol) and potassium carbonate (563mg, 10.06mmol) were combined in DMF (5mL) and stirred at room temperature for 18 hours. The DMF was removed in vacuo and the residue partitioned between diethyl ether (50mL) and water (30mL). The layers were separated and the aqueous extracted with diethyl ether (2x30mL). The combined organic solution was dried over magnesium sulphate and concentrated in vacuo to afford the title compound as a yellow solid which was used without further purification in preparation 75. 1HNMR(400MHz, CDCI3) 5: 4.62-4.65 (m, 2H), 5.35-5.38 (m, 1H), 5.45-5.52 (m, 1H), 6.00-6.13. (m, 1H), 7.00-7.04 (m, 1H), 7.27-7.35 (m, 1H), 10.46 (s, 1H); LRMS APCI m/z 232 [M+H]+
Preparation 75
(3-Allvloxy-2.6-dlchloro-phenyl)-methanol
The product of preparation 74 (~5.03mmol) was dissolved in ethanol (30mL) and sodium
borohydrlde (284mg, "7.79mmol) was added. The reaction mixture was stirred at room
temperature for 30 minutes. The reaction was diluted with water (30mL) and glacial acetic
acid was added dropwise until no further effervescence was observed. The mixture was
extracted with diethyl ether (2x50mL). The combined organic extracts were washed with
65
brine, dried over magnesium sulphate and concentrated in vacuo to afford the title compound as a colourless solid which was used without further purification in preparation 76. 1HNMR(400MHz, CDC13) 6:4.54-4.64 (m, 2H), 4.98 (s, 2H), 5.33-5.38 (m, 1H), 5.43-5.52 (m, 1H), 5.99-6.11 (m, 1H), 6.83-6.88 (m, 1H), 7.24-7.28 (m, 1H).
Preparation 76
1-Allvloxv-2.4-dichloro-3-chloromethvl-benzene
The product of preparation 75 (400mg, 1.72mmol) was dissolved in dichloromethane (20mL)
and thionyl chloride (312^1, 4.29mmol) was added over 1 minute. The reaction mixture was
stirred at room temperature for 10 minutes. The reaction was quenched with water (2x1 OmL).
The organic layer was dried over magnesium sulphate and concentrated in vacuo to afford
the title compound as a yellow solid in 91% yield (390mg)
1HNMR(400MHz, CDCI3) 5: 4.54-4.64 (m, 2H), 4.88 (s, 2H), 5.28-5.37 (m, 1H), 5.42-5.50 (m,
1H), 5.99-6.11 (m, 1H), 6.83-6.91 (m, 1H), 7.24-7.33 (m, 1H).
Preparation 77
5-[3-((3-Allvloxy-2.6-dlchloro-benzvloxy)-azetjdin-1-vl]-S-methvl-2,2-dlphenvl-hexanenitrlle Sodium hydride (60% dispersion in mineral oil, 25mg, 0.629mmol) was added portionwise to an ice-cooled solution of the product of preparation 56 (140mg, 0.419mmol) in N,N-dimethylformamide (2mL) and the mixture was stirred at 0°C for 30 mins. The product of preparation 76 (137mg, 0.546mmol) was added In DMF (1mL) and the mixture was stirred for 18 hour at room temperature. The reaction mixture was then quenched saturated sodium hydrogen carbonate solution (10mL) and the resulting mixture was extracted with diethyl ether (3x50mL). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 98:2:0.2 to afford the title compound as a colourless gum in 87% yield, 200mg.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.28-1.38 (m, 2H), 2.40-2.48 (m, 2H), 3.00-3.10 (m, 2H), 3.20-3.38 (m, 2H), 4.15-4.25 (m, 1H), 4.58-4.62 (m, 2H), 4.68 (s, 2H), 5.26-5.35 (m, 1H), 5.42-5.48 (m, 1H), 6.00-6.08 (m, 1H), 6.82-6.85 (m, 1H), 7.21-7.44 (m, 11H); LRMS APCl m/z 549 [M+H]+
Preparation 78
5-(3-{2.6-Dichloro-3-f((E)-prQDenvnoxv1-benzvloxy}-azetldln-1-yl]-5-methvl-2.2-dlphenvl-hexanolc acid amide
Potassium hydroxide (400mg, 7.14mmol) was added to a solution of preparation 77 (200mg, 0.364mmol) in 3-methyl-3-pentanol (3mL) and the mixture was heated at 120°C for 24 hours. The reaction mixture was then cooled to room temperature, concentrated In vacuo and the residue was partitioned between ethyl acetate (50mL) and water (30mL). The aqueous layer was separated, extracted with ethyl acetate (2x50mL) and the combined organic solution was
Iried over magnesium sulfate and concentrated in vacuo. Recrystallisatlon from liisopropylether gave the title compound as a colourless solid In 73% yield, 150mg. HNMR(400MHz, CDCI3) 5: 0.90 (s, 6H), 1.12-1.20 (m, 2H), 1.72-1.78 (m, 3H), 2.40-2.52 (m, >H), 3.02-3.15 (m, 2H), 3.24-3.40 (m, 2H), 4.15-4.25 (m, 1H), 4.68 (s, 2H), 4.98-5.07 (m, 1H), 5.35-5.63 (brm, 2H), 6.25-6.28 (m, 1H), 6.92-6.95 (m, 1H), 7.21-7.38 (m, 11H); LRWIS ESI n/z 567 [M+H]+
3reparatlon'79
Sulfamlc acid 2-cvclopentvl-ethvl ester
To chlorosulfonyl isocyanate (275mL, 3.15 mol) at 0°C was added formic acid (119mL, 3.15 mol), dropwise. The resulting solid was allowed to stir at 0°C for a further 20 minutes. The residue was diluted with diohloromethane (B75mL) and warmed to room temperature for one hour. The reaction mixture was cooled in an ice/salt bath and a solution of 2-cyclopentyl ethanol (240g, 2.1 mol) in pyridine (255mL, 3.15 mol) and dichloromethane (2.1L) was added, keeping the temperature below 7°C. After 2 hours, the reaction was concentrated in vacuo, diluted with ethyl acetate, washed with saturated sodium bicarbonate solution and brine. The organic layer was dried over sodium sulfate, filtered and concentrated In vacuo to give a colourless oil. The residue was purified by column chromatography on silica gel, eluting with 90:10 to 50:50 heptane:ethyl acetate, to afford the title compound as a colourless oil In 95% yield (276g).
Preparation 80
8-Oxa-7-thla-6-aza-spiror4.51decan67.7-dioxlde
To the product of preparation 79 (276g, 1.43mol) in dichloromethane (7.1 L) at room
temperature were added magnesium oxide (132.5g, 3.29mol), lodobenzene diacetate (507g,
1.57mol) and rhodium acetate dirrier (12.6g, 0.028mol). The reaction mixture was stirred at
room temperature for 18 hours. The residue was filtered through a bed of celite and the
solvent was removed In vacuo. The residue was purified by column chromatography on silica
gel, eluting with 90:10 to 50:50 heptane:ethyl acetate, to afford the title compound as a white
crystalline solid in 75% yield (205g).
1HNMR(400MHz, CDCI3) 5: 1.63-1.78 (m, 4H), 1.79-2.00 (m, 4H), 2.00-2.11 (m, 2H), 4.64-
4.67 (m, 2H), 4.71 (s, 1H); LRMS APCI m/z 214 [M+Na]+
Preparation 81
7.7-Dioxo-8-oxa-7lambda*6*-thia-6-aza-splror4.51decane-6-carboxyllcacldtert-butvlester The product of preparation 80 (1.0g, 5.23mmol), dl-ferf-butyl dicarbonate (1.36g, 6.24mmol), triethyamine (1.06g, 10.5mmol) and 4-dimethylaminepyridine (126mg, 1.03mmol) were combined at room temperature in dichloromethane (50mL). After 3 hours, the reaction was washed with ammonium chloride (50mL, sat. aq.) and the organic solution was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column
chromatography on silica gel, eluting with 100:0 to 80:20 pentane:ethyl acetate, to afford the title compound as a colourless oil in 46% yield (700mg).
'HNMR(400MHz, CDCI3) 5: 1.48 (s, 9H), 1.48-1.66 (m, 2H), 1.82-1.96 (m, 4H), 2.17-2.33 (m, 4H), 4.57-4.63 (m, 2H).
Preparation 82
4-(1-Amlno-cvclopentvl)-2.2-diphenvl-butvrQnitrile
The title compound was prepared from the product of preparation 81 using a similar method
to that described for preparation 55, in 67% yield.
1HNMR(400MHz, CDCI3) 5: 1.43-1.58 (m, 4H), 1.58-1.67 (m, 4H), 1.72-1.80 (m, 2H), 2.49-
2.60 (m, 2H), 7.25-7.46 (m, 10H); LRMS APCI m/z 305[M+H]+
Preparation 83
4-[1-(3-Hvdroxv-azetldin-1-vl)-cvcloDentyn-2.2;diphenvl-butvronitrlle
The title compound was prepared from the product of preparation 82 using a similar method
to that described for preparation 56, in 52% yield.
1HNMR(400MHz, CDCI3) 5: 1.25-1.38 (m, 2H), 1.39-1.64 (m, 6H), 1.65-1.78 (m, 2H), 2.42-
2.55 (m, 2H), 2.86-2.97 (m, 2H), 3.36-3.40 (m, 2H), 4.29-4.40 (m, 1H), 7.25-7.48 (m, 10H);
LRMS APCI m/z 361 [M+H]+
Preparation 84
Methanesulfonic acid 1-ri-(3-cvano-3.3-dlphenvl-propvl)-cvclopentvn-azetidln-3-yl ester
The title compound was prepared from the product of preparation 83 using a similar method
to that described for preparation 57, in 59% yield.
1HNMR(400MHz, CDC13) 5: 1.25-1.67 (m, 10H), 2.42-2.52 (m, 2H), 3.00 (s, 3H), 3.15-3.26
(m, 2H), 3.40-3.55 (m, 2H), 4.95-5.05 (m, 1H), 7.27-7.45 (m, 10H); LRMS APCI m/z 439
[M+H]+
Preparation 85
5-[3-(3-Allvlqxv-4-chloro-benzvloxv)-azetidln-1-yl]-5-methvl-2.2-dlphenvl-hexanenitrlle The title compound was prepared from the product of preparation 56 and the product of preparation 42 using a similar method to that described for example 101, in 83% yield. 1HNMR(400MHz, CDCI3) 6: 0.92 (s, 6H), 1.32-1.38 (m, 2H), 2.40-2.48 (m, 2H), 2.97-3.06 (m, 2H), 3.23-3.32 (m, 2H), 4.05-4.16 (m, 1H), 4.36 (s, 2H), 4.58-4.65 (m, 2H), 5.28-5.35 (m, 1H), 5.43-5.63 (m, 1H), 6.02-6.16 (m, 1H), 6.80-6.85 (m, 1H), 6.92.(s, 1H), 7.23-7.42 (m, 11H); LRMS APCI m/z 515 [M+H]+
Preparation 86
5-(3-l4-Chloro-3-r((EVDropenvnoxv1-benzvloxy}-azetidln-1-yl]-5-methvl-2.2-dlphenvl-hexanoic acid amide
The title compound was prepared from the product of preparation 85 using a similar method to that described for preparation 73, in 75% yield. LRMS APC! m/z 533 [M+H]+
Preparation 87
4-{1-r3-f3-Allvloxv-4-chloro-phenoxy)-azetldln-1-yl]-cvclopenttl}-2.2-dlPhenvl-butvronitrile The title compound was prepared from the product of preparation 84 and 3-allyloxy-4-chlorophenol (EP78099) using a similar method to that described for example 99, in 82% yield.
1HNMR(400MHz, CDCI3) 5: 1,25-140 (m, 2H), 1.40-1.65 (m, 6H), 1.66-1.77 (m, 2H), 2.46-2.58 (m, 2H), 3.07-3.16 (m, 2H), 3.46-3.58 (m, 2H), 4.55-4.59 (m, 2H), 4.60-4.73 (m, 1H), 5.26-5.35 (m, 1H), 5.43-5.53 (m, 1H), 6.00-6.13 (m, 1H), 6.20-6.28 (m, 1H), 6.42 (s, 1H), 7.19-7.23 (m, 1H), 7.23-7.46 (m, 10H); LRMS APCI m/z 527 [M+H]+
Preparation 88
4-[1-(3-{4-Chloro-3-f((E)-proDenvnoxv]-phenoxv}-azetldin-1-yn-cvclopentyn-2.2-dlphenvl-
butvramide
The title compound was prepared from the product of preparation 87 using a similar method
to that described for preparation 73, In 49% yield,
LRMS APCI m/z 545 [M+H]+
Preparation 89
3-Bromo-S-methoxv-phenol
1-bromo-3,5-dlmethyoxybenzene (3.0g, 13.8mmol) was dissolved in dichloromethane (45mL)
and the solution was cooled to -78°C. Boron tribromide (1M in dichloromethane, 41 mL,
41mmol) was added and the solution was warmed gradually to room temperature over 18
hours. After cooling to -78°C, the reaction was quenched with water (100mL). The organics
were separated and washed with sodium thiosulphate solution then water, then dried over
magnesium sulfate and concentrated in vacuo. The residue was purified by column
chrpmatography on silica gel, eluting with pentane:ethyl acetate 100:0 to 80:20, to afford the
title compound in 16% yield (470mg).
1HNMR(400MHz, MeOD) 5: 3.76 (s, 3H), 6.28 (s, 1H), 6.53-6.57 (m, 2H).
Preparation 90 4-Allvloxv-3-chloro-benzaldehyde
The title compound was prepared from 3-chloro-4-hydroxybenzaldehyde using a similar method to that described for preparation 74, in 96% yield. The material was used without further purification in preparation 91.
1HNMR(400MHz, CDCI3) 6: 4.68-4.76 (m, 2H), 5.35-5.39 (m, 1H), 5.44-5.56 (m, 1H), 6.02-6.15 (m, 1H), 7.01-7.05 (m, 1H), 7.76-7.79 (m, 1H), 7.93 (s, 1H), 9.86 (s, 1H); LRMS APCI . m/z197[M+H]+
Preparation 91
(4-Allvloxv-3-chloro-phenvh-methanol
The title compound was prepared from the product of preparation 90 using a similar method
to that described for preparation 76, In 100% yield. The material was used without further
purification in preparation 92.
1HNMR(400MHz, CDCI3) S: 4.61-4.65 (m, 4H), 5.28-5.36 (m, 1H), 5.44-5.52 (m, 1H), 6.02-
6.13 (m, 1H), 6.88-6.94 (m, 1H), 7.17-7.20 (m, 1H), 7.40 (s, 1H).
Preparation 92
1-Allvloxv-2-chloro-4-chloromethvl-benzene
The title compound was prepared from the product of preparation 91 using a similar method
to that described for preparation 76, in 70% yield. The material was used without further
purification'in preparation 94.
1HNMR(400MHz, CDCI3) 5: 4.52 (s, 2H), 4.60-4.63 (m, 2H), 5.28-5.35 (m, 1H), 5.43-5.54 (m,
1H), 6.01-6.12 (m, 1H), 6.86-6.94 (m, 1H), 7.20-7.24 (m, 1H), 7.42 (s, 1H).
Preparation 93
5-( 3-Hydroxy-azetidln-1 -yl)-5-methvl-2.2-dlphenvl-hexanoic acid arnlde
The product from example 102 (5.2g, 12.2mmol), ammonium formate (4.25g, 92mmol) and
palladium hydroxide 20 wt % Pd on carbon (1.7g) were combined in ethanol (150mL) and
stirred at reflux for one hour. After cooling, the residue was filtered through Arbocel0, washing
with MeOH (50mL). The filtrate was concentrated in vacuo. The residue was diluted with
ethyl acetate (100mL) and washed with sodium hydrogen carbonate solution (30mL, sat. aq.).
The organic extract was dried over magnesium sulfate and concentrated in vacuo. The title
compound was isolated as a colourless foam in 97% yield, 4.2g.
1HNMR(400MHz, CDCI3) 8: 0.94 (s, 6H), 1.08-1.18 (m, 2H), 2.35-2.45 (m, 2H), 2.85-2.95 (m,
2H), 3.26-3.35 (m, 2H), 4.25-4.35 (m, 1H), 5.56-5.80 ( br m, 2H), 7.15-7.40 (m, 10H); LRMS
ESI m/z 353 [M+H]+
Preparation 94
5-[3-(4-Allvloxv-3-chloro-benzyloxyVazetldln-1-vl]-S-methvl-2.2-diphenvl-hexanolc acid amide The product of preparation 93 (300mg, 0.85mmol) was dissolved in DMF at 0°C (5mL) and sodium hydride (60% dispersion in oil, 62mg, 1.6mmol) added. After 30 minutes, a solution of the product of preparation 92 (210mg, 1.15mmol) in DMF (1mL) was added. After 30 minutes, the reaction was quenched with 2N HCI (20ml), basifled with saturated sodium hydrogen carbonate and the product extracted with ethyl acetate (20mL). The organic extract
was dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:meth'anol:0.88 ammonia, 100:0:0 to 90:10:1, afforded the title compound as a colourless oil in 22% yield, 100mg. 1HNMR(400MHz, CDCI3) 6: 0.92 (s, 6H), 1.11-1.20 (m, 2H), 2.39-2.47 (m, 2H), 2.98-3.08 (m, 2H), 3.23-3.39 (m, 2H), 4.08-4.17 (m, 1H), 4.28 (s, 2H), 4.58-4.63 (m, 2H), 5.27-5.35 (m, 1H), 5.45r5.50 (m/IH), 5.40-5.60 (br m, 2H), 6.01-6.13 (m, 1H), 6.85-6.92 (m, 1H), 7.07-7.15 (m, 1H), 7.20-7.37 (m, 11H); LRMS ESI m/z 533
Preparation 95
2^-Allvloxy-4-chloro-benzaldehvde
The title compound was prepared from 4-chloro-2-hydroxybenzaldehyde using a similar
method to that described for preparation 74, in 85% yield. The material was used without
further purification In preparation 96.
1HNMR(400MHz, CDCI3) 6: 4.62-4.66 (m, 2H), 5.35-5.39 (m, 1H), 5.40-5.46 (m, 1H), 6.02-
6.13 (m, 1H), 6.92-6.96 (m, 1H), 7.45-7.51 (m, 1H), 7.80 (s, 1H), 10.45 (s, 1H); LRMS APCI
m/z 1_97 [M+H]+
Preparation 96
(2-Allyloxy-4-chloro-phenvh-methano!
The title compound was prepared from the product of preparation 95 using a similar method
to that described for preparation 75, in 100% yield. The material was used without further
purification in preparation 97.
1HNMR(400MHz, CDCI3) 6: 4.55-4.60 (m, 2H), 4.67 (s, 2H), 5.28-5.35 (m, 1H), 5.38-5.45 (m,
1H), 5.98-6.08 (m, 1H), 6.76-6.83 (m, 1H), 7.17-7.21 (m, 1H), 7.33 (s, 1H).
Preparation 97
2-Allvloxy-4-chloro-1-chloromethvl-benzene
The title compound was prepared from the product of preparation 96 using a similar method
to that described for preparation 76, in 77% yield. The material was used without further
purification in preparation 98
1HNMR(400MHz, CDCI3) 6: 4.57-4.60 (m, 2H), 4.62 (s, 2H), 5.28-5.35 (m, 1H), 5.40-5.47 (m,
1H), 6.00-6.09 (m, 1H), 6.78-6.83 (m, 1H), 7.20-7.25 (m, 1H), 7.37 (s, 1H).
Preparation 98 5-[3-((2-Allvloxv-4-chloro-benzvloxy)-azetidin-1-yl]-5-methvl-2.2-diphenvl-hexanoic acid amide
The title compound was prepared from the products of preparation 97 and 93 using a similar method to that described for preparation 94, in 16% yield.
1HNMR(400MHz, CDCI3) 5: 0.92 (s, 6H), 1.10-1.98 (m, 2H), 2.38-2.45 (m, 2H), 2.98-3.08 (m, 2H), 3.28-3.39 (m, 2H), 4.10-4.20 (m, 1H), 4.40 (s, 2H), 4.47-4.55 (m, 2H), 5.23-5.32 (m, 1H),
5.35-5.41 (m, 1H), 5.53-5.86 (br m, 2H), 5.97-6.08 (m, 1H), 6.73-6.78 (m, 1H), 7.14-7.20 (m, 1H), 7.20-7.39 (m, 11H); LRMS ESI m/z 533 [M+H]+
Preparation 99
3-Allyloxy-2-chloro-benzaldehvde
The title compound was prepared from 2-chloro-3-hydroxybenzaldehyde using a similar
method to that described for preparation 74, En 100% yield. The material was used without
further purification in preparation 100. Preparation 100
(3-Allvloxv-2-chloro-phenvlV-methanol
The title compound was prepared from the product of preparation 99 using a similar method
to that described for preparation 31, in 92% yield. The material was used without further
purification in preparation 101.
1HNMR(400MHz, CDCl3) 5:4.62-4.66 (m, 2H), 4.78 (s, 2H), 5.32-5.37 (m, 1H), 5.46-5.52 (m,
1H), 6.02-6.15 (m, 1H), 6.86-6.94 (m, 1H), 7.07-7.14 (m, 1H), 7.20-7.28 (m, 1H).
Preparation 101
1-Allvloxy-2-chloro-3-chloromethyl-benzene
The product of preparation 100 (740mg, 3.73mmol) was dissolved in dichloromethane (20mL)
and thionyl chloride (678)11, 9.32mmol) was added over 1 minute. The reaction mixture was
stirred at room temperature for 2 hours. A further 600µl thionyl chloride was added and the
reaction stirred for 1 hour. The reaction was quenched with water (10mL). The organic layer
was washed with saturated sodium hydrogen carbonate solution (20mL) and water (10mL.),
dried over magnesium sulphate and concentrated in vacuo. Purification of the residue by
column chramatography on silica gel, eluting with pentane:ethyl acetate 100:0 to 99:1
afforded the title compound as a colourless oil in 21% yield, 168mg.
1HNWlR(400MHz, CDCI3) 6: 4.59-4.68 (m, 2H), 4.75 (s, 2H), 5.28-5.37 (m, 1H), 5.44-5.55 (m,
1H), 6.00-6.15 (m, 1H), 6.86-6.95 (m, 1H), 7.06-7.13 (m, 1H), 7.17-7.26 (m, 1H).
Preparation 102
5-[3-(3-Allvloxv-2-chloro-benzvloxy)-azetidln-1-yl]-5-methvl-2.2-dlphenvl-hexanenltrlle
The title compound was prepared from the products of preparations 101 and 56 using a
similar method to that described for example 101, in 69% yield.
1HNMR(400MHz, CDCI3) 6: 0.95 (s, 6H), 1.29-1.38 (m, 2H), 2.40-2.52 (m, 2H), 3.02-3.15 (m,
2H), 3.24-3.39 (m, 2H), 4.15-4.22 (m, 1H), 4.53 (s, 2H), 4.60-4.64 (m, 2H), 5.28-5.35 (m, 1H),
5.45-5.50 (m, 1H), 6.03-6.15 (m, 1H), 6.86-6.90 (m, 1H), 7.05-7.08 (m, 1H), 7.16-7.23 (m,
1H), 7.23-7.45 (m, 10H); LRMS APCI m/z 515 [M+H]+
Preparation 103 5-[3-{2-Chloro-3.r((E)-propenvl)oxy]-1-benzvlQxv\-azetidln-1-yl]-5-methvl-2.2-diphenvl-h6xanolc
acid amide
The title compound was prepared from the product of preparation 102 using a similar method
to that described for preparation 78, in 61 % yield.
1HNMR(400MHz, CDCI3) 6: 0.95 (s, 6H), 1.19-1.20 (m, 2H), 1.72-1.78 (m, 3H), 2.40-2.48 (m,
2H), 3.02-3.15 (m, 2H), 3.20-3.42 (m, 2H), 4/13-4.25 (m, 1H), 4.53 (s, 2H), 4.95-5.03 (m, 1H),
5.32-5.60 (brm, 2H), 6.30-6.45 (m, 1H), 6.93-6.97 (m, 1H), 7.12-7.40 (m, 12H); LRMS ESI
m/z 533 [M+H]+
Preparation 104
Methanesulfonlc acid 1-(4-carbamovl-1.1-dimethvl-4.4-diphenvl-butvll-azetidln-3-yl ester Methane sulfonyl chloride (102uL, 1.33mmol) was added dropwise to a solution of the product of preparation 93 (158mg, 0.44mmol) in pyridine (5mL), cooled to -20°C. The mixture was warmed gradually to 5°C over.2.hours. Saturated sodium hydrogen carbonate solution (10mL) was added and the reaction mixture stirred at room temperature for 10 minutes. The residue was extracted with ethyl acetate (3x30mL) and the combined organlcs were dried over magnesium sulphate, filtered and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethylacetate/methanol/0.88 ammonia (90/10/1) 8:1 to 1:2, afforded the title compound as a colourless oil in 74% yield, 142mg.
1HNMR(400MHz, CDCI3) 5: 0.88 (s, 6H), 1.08-1.15 (m, 2H), 2.38-2.45 (m, 2H), 2.98 (s, 3H), 3.07-3.22 (m, 2H), 3.36-3.52 (m, 2H), 4.95-5.00 (rti, 1H), 5.42-5.53 (br m, 1H), 5.71-5.80 (br m, 1H), 7.23-7.38 (m, 10H); LRMS ESI m/z 431 [M+H]+
Preparation 105
5-[3-(3-Ben2Vloxv-phenoxy)-azetldin-1-yl]-S-methvl-2.2-diphenvl-hexanenitrilB
The title compound was prepared from the product of preparation 57 and 3-
(benzyloxy)phenol, using the same method as that described in example 99, as a yellow oil in
95% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.35-1.42 (m, 2H), 2.40-2.52 (m, 2H), 3.09-3.20 (m,
2H), 3.40-3.52 (m, 2H), 4.61-4.72 (m, 1H), 5.06 (s, 2H), 6.36-6.40 (m, 2H), 6.57-6.62 (m, 1H),
7.10-7.18 (m, 1H), 7.15-7.47 (m, 15H); LRMS APCI m/z 517 [M+H]+
Preparation 106
(4-Allvloxy-Phenyn-methanol
The title compound was prepared from the 4-hydroxybenzyl alcohol using a similar method to
that described for preparation 74, In 57% yield.
1HNMR(400MHz, CDCI3) 5: 4.52-4.94 (m, 2H), 4.63 (s, 2H), 5.28-5.35 (m, 1H), 5.38-5.45 (m,
1H), 6.00-6.12 (m, 1H), 6.86-6.94 (m, 2H), 7.24-7.33 (m, 2H).
Preparation 107
1-Allvloxy-4-chloromethvl-benzene
The title compound was prepared from the product of preparation 106 using a similar method
to that described for preparation 76 in 43% yield.
1HNMR(400MHz, CDCI3) 6: 4.53-4.58 (m, 4H), 5.25-5.32 (m, 1H), 5.36-5.43 (m, 1H), 6.00-
6.12 (m, 1H), 6.86-6.94 (m, 2H), 7.28-7.35 (m, 2H)
Preparation 108
5-[3-((4-Allvloxv-ben2Vloxv)-azetldln-1-yl]-5-methvl-2.2-diphenvl-hexanolc acid amide
The title compound was prepared from the products of preparations 107 and 93 using a
similar method to that described for preparation 94, in 25% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.24-1.28 (m, 2H), 2.35-2.45 (m, 2H), 2.94-3.00 (m,
2H), 3.20-3.28 (m, 2H), 4.06-4.15 (m, 1H), 4.35 (s, 2H), 4.52-4.55 (m, 2H), 5.25-5.28 (m, 1H),
5.36-5.43 (m, 1H), 5.40-5.60 (br m, 2H), 6.00, 6.12 (m, 1H), 6.84-6.89 (m, 2H), 7.20-7.38 (m,
12H); LRMS APCI m/z 499 [M+H]+
Example 1 5-Methvl-5-[f3SV3-phenoxvpvrrolidin-1-yl]-2.2-diphenvlhexanenitrile
(Formula Removed)
A solution of the product of preparation 11 (3.31 g, 8.07mmol) in tetrahydrofuran (90mL) was cooled to -20°C. Zirconium chloride (3.76g, 16.15mmol) was added and the reaction mixture was stirred at -20°C for 1 hour. Methyl magnesium chloride (3M in tetrahydrofuran,- 24mL, 72mmol) was then added dropwise and the mixture was stirred for 2 hours, with the temperature maintained below-10°C. The reaction was quenched with 1M aqueous sodium hydroxide solution (25mL) and then filtered through Celite* washing through with ethyl acetate (2x50mL). The filtrate was washed with brine (70mL), concentrated in vacuo and the residue was re-crystallised from hexane/ethyl acetate to afford the title compound as a pale orange crystalline solid in 59% yield, 2g.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.04(S, 3H), 1.23-1.27(m, 2H), 1.85-1.93(m, 1H), 2.07-2.16(m, 1H), 2.40-2.45(m, 2H), 2.58-2.67(m, 2H), 2.72-2.78(m, 1H), 2.87-2.91(m, 1H), 4.75-4.79(m, 1H), 6.80(d, 2H), 6.88-6.92(m, 1H), 7.21-7.36(m, 12H); LRMS APCI m/z 425 [M+H]+
(Formula Removed)
Example 2 5-MIethyl-5-[(3S)-3-phenpxvpyrrolidin-1-vl]-2.2-diphenvlhexanamide
Potassium hydroxide (5.10g, 91.98mmol) was added to a solution of the product of example 1 (1.95g, 4.60mmol) in 3-methyl-3-pentanol (40mL) and the mixture was heated under reflux for 24 hours. The reaction mixture was then cooled to room temperature, concentrated in vacuo and the residue was partitioned between ethyl acetate (70mL) and water (40mL). The aqueous layer was separated, extracted with ethyl acetate (50mL) and the combined organic solution was dried over sodium sulfate and concentrated in vacuo. The residue was then re-crystallised from hexane/ethyl acetate and dried under vacuum for 18 hours to afford the title compound as a white solid in 82% yield, 1.66g.
1HNMR(400MHz, CD3OD) 5: 0.97(3, 3H), 1.02(s, 3H), 1.19-1.33(m, 2H), 1.82-1.91 (m, 1H), 2.02-2.17(m, 1H), 2.37-2.47(m, 2H), 2.48-2.64(m, 2H), 2.65-2.75(m, 1H), 2.81-2.89(m, 1H), 4.75(m, 1H), 6.76-6.83(m, 2H), 6.86-6.92(m, 1H), 7.17-7.38(m, 12H); LRMS APCI m/z 425 [M+H]+*
Example 3 5-Methvl-5-[(3RV3-phenoxvpvrrolidin-1-yl]-2.2-diphenvlhexanenitrilB
(Formula Removed)
A solution of the product of preparation 12 (0.84g, 2.05mmol) in tetrahydrofuran (15mL) was cooled to -10°C. Titanium (IV) chloride (0.23mL, 2.05mmol) was added and the reaction mixture was stirred at-10°C for 15 minutes. Methyl magnesium bromide (3M, in diethyl ether, 4.1mL, 12,3mmol) was then added dropwise and the mixture was stirred for 10 minutes at temperatures below -5°C and at room temperature for 18 hours. The reaction mixture was slowly quenched with water (4mL), diluted with ethyl acetate (20mL) and then decanted off. The residual solid was extracted with ethyl acetate (3x 20mL) and the combined organic
solution was dried over sodium sulphate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with ethyl acetate:hexane, 60:40, afforded the title compound in 54% yield, 0.47g. LRMSAPCIm/z425[M+H]+
Exampje 4 5-Methvl-5-[f3RV3-phenoxvpvrrolidin-1-yl]-2.2-dlphenvlhexanamlde
(Formula Removed)
The title compound was prepared from the product of example 3, using the same method as that described for example 2, in 62% yield. LRMS APCI m/z 443 [M+H]+
Example 5 5-[(3S)3-(3-Methoxvphejoxv^pvrrolidin-1-yl]-5-methvl-2.2-diphenvlhexanenitrile
(Formula Removed)
The title compound was prepared from the product of preparation 13, using the same method as that described for example 1. The. crude compound was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 97.5:2.5:0.25 to 95:5:0.5, to afford the desired product as a brown oil in 78% yield. 1HNMR(400MHz, CD3OD) 6: 1.01(s, 3H), 1.07(s, 3H), 1.43-1.47(m, 2H), 1.86-1.93(m, 1H), 2.08-2.19(m, 1H), 2.47-2.59(m, 3H), 2.65-2.69(m, 1H), 2.73-2.86(m, 2H), 3.73(s, 3H), 4.74-4.79(m, 1H), 6.38-6.43(m, 2H), 6.47-6.50(m, 1H), 7.11-7.15(m, 1H), 7.24-7.42(m, 10H); LRMS APCI m/z 456 [M+H]+
Example 6
5-[{3S)-3-(3-methoxvphenoxy)avrrolidln-l-yl]-6-methvl-2,2-dlphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 5, using the same method as that described for example 2, as a pale yellow gum in 96% yield.
1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.08(s, 3H), 1 .24-1 .30(m, 2H), 1.89-1.98(m, 1H), 2.08-2.16(m, 1H), 2.40-2.46(m, 2H), 2.65-2.76(m, 2H), 2.79-2.88(m, 1H), 2.91-2.98(m, 1H), 3.74(3, 3H), 4.77-4.82(m, 1H), 6.37-6.42(m, 2H), 6.51(dd, 1H), 7.12-7.16(m, 1H), 7.22-7.36(m, 10H); LRMS APCI m/z 474 [M+H]+
Example? 5-[(3S)-3-(3-HvdroxvPhenoxv)pvrrolldin-1-vl1-5-methvl-2.2-diPhenvlhexanamide
(Formula Removed)
Boron trlbromlde (1M in dichloromethane, 20.7mL, 20.7mmol) was added to an ice-cooled solution of the product of example 6 (2.45g, 5.18mmo!) in dichloromethane (25mL) and the mixture was stirred at 0°C for 20 minutes. The reaction was then quenched with 0.88 ammonia solution and stirred at room temperature for 20 minutes. The reaction mixture was extracted with dichloromethane (3x25mL) and the combined organic solution was dried over sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentaneiethyl acetate/methanol/0.88 ammonia (90:10:1), 50:50 to 33:66, afforded the title compound as a white foam in 60% yield, 1.42g. 1HNMR(400MHz, CD3OD) 5: 1.06(s, 3H), 1.11(8, 3H), 1.30-1.34(m, 2H), 1.94-2.01(m, 1H), 2.08-2.17(m, 1H), 2.42-2.46(m, 2H), 2.77-2.93(m, 3H), 2.99-3.05(m, 1H), 4.79(m, 1H), 6.30(d, 2H), 6.37-6.40(d, 1H), 7.02-7.06(m, 1H), 7.23-7.36(m, 10H); LRMS APCI m/z459 [M+H]+
Example 8 5-[(3R)-3-(Benzvloxy)pvrrolldin-1-yl]-5-methvl-2.2-dlphenvlhexanenitrile
(Formula Removed)
A solution of the product of preparation 15 (40g, 93mmol) in tetrahydrofuran (1L) was cooled to -30°C. Zirconium chloride (44g, 186mmol) was added and the reaction mixture was stirred at -30°C for 1 hour. Methyl magnesium chloride (3M in tetrahydrofuran, (500mL, 900mmol) was then added dropwise and the mixture was stirred for 2 hours, with the temperature maintained below -10°C. The reaction was quenched with 1M aqueous sodium hydroxide solution ((300mL) and the mixture was then decanted off. The residual solid was extracted with ethyl acetate (2x (500mL) and the combined organic solution was evaporated under reduced pressure. The residue was then dissolved in dichloromethane (1L), washed with water (200mL) and concentrated in vacuo. The crude material was purified by column chromatography on silica gel, eluting with dichloromethane:methanol, 97.5:2.5, and the subsequent residue azeotroped with pentane (2x 250mL), diethyl ether (2x 250mL) and pentane (2x 250mL) to afford the title compound as a solid.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 3H), 1.04(8, 3H), 1.42-1.54(m, 2H), 1,78-1.86(m, 1H), 1.93-2.02(m, 1H), 2.47-2.60(m, 3H), 2.63-2.77(m, 3H), 4.04-4.08(m, 1H), 4.43-4.49(s, 2H), 7.23-7.43(m, 15H); LRMS APCI m/z 439 [M+H]+
Example 9 5-[(3R)3-(Ben2vloxvbvrrolidln-1-vl1-5-methvl-2.2-dlPhenvlhexanarnide
(Formula Removed)
The title compound was prepared from the product of example 8, using the same method as that described for example 2, as a solid In 89% yield.
1HNMR(400MHz, CD3OD) 5: 0.99-1. 01 (m, 6H), 1.24-1.28(m, 2H), 1.75-1.82(m, 1H), 1.88-•1.97(m, 1H), 2.40-2.44(m, 2H), 2.49-2.68(m, 2H), 2.71-2.76(m, 1H), 4.00-4.05(m, 1H), 4.39-4.46(m, 2H), 7.22-7.38(m, 15H); LRMS APCI m/z 425 [M+H]+
Example 10 5-[(3S)-3-menzvloxvtovrrolidin-1-yl]-5-methvl-2.2-dlphenvlhexanenltrile
(Formula Removed)
The title compound was prepared from the product of preparation 14, using the same method as that described for example 1. The crude compound was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 99:1:0.1 to 92:8:0.8, to afford the desired product as a brown oil in 76% yield. 1HNMR(400MHz, CD3OD) 5: 1.02(s, 3H), 1.04(8, 3H), 1.4l-1.55(rn, 2H), 1.77-1.85(m, 1H), 1.93-2.01(m, 1H), 2.50-2.55(m, 3H), 2.63:2.77(m, 3H), 4.03-4.08(m, 1H), 4.45(s, 2H), 7.22-7.42(m, 15H); LRMS APCI m/z 439 [M+H]+
Example 11 5-K3SV3-(Benzvloxvtovrrolidln-1-vl1-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 10, using the same method as that described for example 2. The crude compound was purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:0.88 ammonia, 98:2:0.2 to afford the desired product as a colourless gum in 78% yield.
1HNMR(400MHz, CD3OD) 6: 0.98(s, 3H), 1.00(s, 3H), 1.23-1.27(m, 2H), i.73-1.80(m, 1H), 1.87-1.96(11), 1H), 2.40-2.65(m, 5H), 2.69-2.73(m, 1H), 3.98-4.03(m, 1H), 4.42(m, 2H), 7.22-7.32(m, 11H)', 7.35-7.38(m, 4H); LRMS APCI m/z 458 [M+H]+
Example 12 5-[(3RV3-f3-Methoxvphenoxvbvrrolidln-1-yl]-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
A solution of triphanyl phosphine (272mg, 1.04mmol) In tetrahydrofuran (3mL) and dl-Isopropylazodicarboxylate (0.20mL, 1.04mmol) were added to a solution of the product of preparation 16 (190mg, 0.52mmol) in tetrahydrofuran (2mL) and the mixture was stirred at room temperature for 15 minutes. A solution of 3-methoxyphenol (129mg, 1.04mmol) in tetrahydrofuran (2mL) was added and the mixture was stirred at room temperature for 2.5 hours. The reaction mixture was then concentrated In vacuo and the residue was purified by •column chromatography on silica gel, elutlng with dichloromethane:methanol, 95:5 to 90:10, to afford the title compound as a colourless oil In 7% yield, 20mg.
1HNMR(400MHz, CD3OD) 6: 1.05(8, 3H), 1.10(s, 3H), 1.18-1.37(m, 2H), 1.92-2.00(m, 1H), 2.10-2.16(m, 1H), 2.40-2.45(m, 2H), 2.72-2.95(m, 3H), 2.97-3.05(m, 1H), 3.74(s, 3H), 4.80-4.14(m, 1H), 6.38-6.40(m, 2HJ, 6.51(d, 1H), 7.12-7.16(m, 2H), 7.22-7.37(m, 9H); LRMS APCI m/z472[Wl+Hf
Example 13 5-[(3RW3-(3-Hvdroxvphenoxv)pvrrolidln-1-yl]-S-methvl-2.2-diphenvlhexanamide
(Formula Removed)
Boron tribromide (1M In dichloromethane, 0.17mL, 169mmol) was added to a solution of the product of example 12 (20mg, 42mmol) in dichloromethane (2mL) and the mixture was stirred at room temperature. The reaction was monitored by tic analysis and portions of boron tribromide (1M in dichloromethane, 0.17mL, 42mmol) were added at regular Intervals until all of the starting material had been consumed. After a period of 8 days, the reaction mixture was quenched with 0.88 ammonia solution, stirred at room temperature for 1 hour then extracted with dichloromethane (3x5mL). The combined organic solution was dried over sodium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 92:8:0.8. The appropriate fractions were evaporated under reduced pressure and the residue was dissolved in ethanol. Ammonium formate (12mg, 0.19mmol) and 20% Pd(OH)z/C (2mg) were added and the mixture was heated under reflux for 4 hours. The reaction mixture was then cooled to room temperature, filtered through Arbocel®and the filtrate was concentrated in vacuo. The filtrate was partitioned between ethyl acetate (8mL) and aqueous ammonia solution (2mL) and the aqueous layer was separated and extracted with further ethyl acetate (2x3mL). The combined organic solution was dried over sodium sulfate, concentrated In vacuo and the residue was purified by column chromatography on silica gel, eluting with dlchloromethane:methanol:0.88 ammonia, 95:5:0.5, to afford the title compound as a colourless gum in 68% yield, 5.8mg.
1HNMR(400MHz, CD3OD) 5: 0.99(s, 3H), 1.05(s, 3H), 1.23-1.28(m, 2H), 1.85-1.90(m, 1H), 2.06-2.1 2(m, 1H), 2.40-2.45(m, 2H), 2.57-2.69(m, 2H), 2.72-2.79(m, 1H), 2.85-2.90(m, 1H), 4.70-4.73(m, 1H), 6.26-6.30(m, 2H), 6.36(d, 1H), 7.00-7.04(m, 1H), 7.21-7.25(m, 2H), 7.27-7.31 (m, 4H), 7.33-7.36(m, 4H); LRMS ESI m/z 459 [M+H]+
Example 14 5-M6thvl-5-[/3SV3-r3-methvlphenoxvtovrrolldln-1-yl]-2.2-dlphenvlhexanamlde

(Formula Removed)
Di-isopropylazodicarboxylate (65µL, 0.34mmol) and the product of preparation 17 (62mg, 0.17mmol) were added to a solution of triphenyl phosphine (89mg, 0.34mmol) in tetrahydrofuran (5mL) and the mixture was stirred at room temperature for 15 minutes. A solution of 3-methylphenol (27mg, 0.25mmol) in tetrahydrofuran (1mL) was added and the mixture was stirred at room temperature for 2 hours. The reaction mixture was then concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethana:methanol, 100:0 to 93:7, to afford the title compound as a colourless gum in 43% yield, 33mg.
1HNMR(400MHz, CD3OD) 5: 0.97(s, 3H), 1.03(s, 3H), 1.21-1.26(m, 2H), 1.82-1.90(m, 1H), 2.05-2.13(01, 1H), 2.27(s, 3H), 2.40-2.45(m, 2H), 2.51-2.61(m, 2H), 2.68-2.74(m, 1H), 2.81-2.85(m, 1H), 4.71-4.75(m, 1H), 6.57-6.62(m, 2H), 6.72(d, 1H), 7.08-7.12(m, 1H), 7.35-7.20(m, 10H); LRMS APCI m/z 457 [M+H]+
Example 15
5-[(3RV3-(1.3-Benzoxazol-6-vloxv^Dvrrolldln-1-yl]-5-methvl-2,2-dlphenvlhexanamide
(Formula Removed)
Diethyl azodicarboxylate (125µL, 0.74mmol) and a solution of 6-benzoxazolol [(100mg, 0.74mmol), US 613027, p56] in tetrahydrofuran (2mL) were added to an ice-cooled solution of triphenyl phosphine (195mg, 0.74mmol) in tetrahydrofuran (2mL) and the mixture was stirred at 0°C for 10 minutes and at room temperature for 90 minutes. A solution of the product of
preparation 16 (238mg, 0.65mmol) in tetrahydrofuran (2mL) was then added and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then partitioned between ethyl acetate and dilute sodium carbonate solution and the aqueous layer was separated and extracted with ethyl acetate (x2). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with d!chloromethane:methanol, 90:10 to afford the title compound In 29% yield, 90mg. LRMS APCI m/z 484 [M+H]+
Examples 16 and 17
The following compounds, of the general formula shown below, were prepared using the same method to that described for example 15, using the product of preparation 17 and commercially available phenols. The reactions were monitored by tic analysis and were stirred at room temperature for 18-96 hours.

(Table Removed)
Example 18 5-[(3S)3-f(3'-Hvdroxvbiphenvl-4-vnoxvlDvrrolidln-1-yl)-S-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
Di-lsopropylazodicarboxylate (0.21 mL, 1.09mmol) and the product of preparation 17 (218mg, 1.09mmol) were added to a solution of triphenyl phosphine (286mg, 1.09mmol) In tetrahydrofuran (5mL) and the mixture was stirred at room temperature for 15 minutes. A solution "of 3-methoxy-1,1'-biphenyl-4-ol [(200mg, 0.55mmol) Bioinorganic and Medicinal Chemistry, 2003, 11, 2347] in tetrahydrofuran (2mL) was added and the mixture was stirred at room temperature for 4 hours. The reaction mixture was then concentrated in vacuo and the residue was purified by column chromatography on silica gel, elutlng with dichloromethaneimethanol, 100:0 to 93:7. The appropriate fractions were evaporated under reduced pressure and the residue was further purified by column chromatography on silica gel, eluting with pentane:ethyl acetate/methanol/0.88 ammonia (90:10:1), 100:0 to 50:50. The appropriate fractions were concentrated in vacuo and the residue was dissolved in dichloromethane (2mL). Boron tribromide (1M In dichloromethane, 0.58mL, 0.58mmol) was added and the mixture as stirred at room temperature for 90 minutes. The reaction was then quenched by the dropwise addition of 0.88 ammonia solution and the mixture was stirred at room temperature for a further 30 minutes. The reaction mixture was then extracted with dichloromethane (3x20mL) and the combined organic solution was concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethyl acetate/methanol/0.88 ammonia (90:10:1), 100:0 to 50:50, to afford the title compound as a foam in 5% yield, 14mg.
1HNMR(400MHz, CD3OD) 5: 0.96(s, 3H), 1.04(s, 3H), 1.21-1.26(m, 2H), 1.86-1.93(m, 1H), 2.10-2.15(m, 1H), 2.39-2.46(m, 2H), 2.52-2.57(m, 1H), 2.62(dd, 1H), 2.70-2.76(m, 1H), 2.83(dd, 1H), 4.73-4.79(m, 1H), 6.70-6.72(dd, 1H), 6.84-6.87(m, 2H), 6.97-7.02(m, 2H), 7.18-7.57(m, 13H); LRMS APCI m/z 535 [M+H]+
Example 19 5-((3S)3-r(3'-Hvdroxvbiphenvl-3-vnoxvlPvrrolidln-1-yl)-5-methvl-2.2-dlphenvlhexanamtde
(Formula Removed)
The title compound was prepared from the product of preparation 17 and 3-methoxy-1,1'-biphenyl-3-ol [WO 2003 006437, p45], using the same method as that described for example 18, as a colourless gum in 16% yield.
1HNMR(400MHz, CD3OD) 6: 0.98(s, 3H), 1.03(s, 3H), 1.21-1.25(m, 2H), 1.87-1.94(m, 1H), 2.09-2.18(m, 1H), 2.40-2.45(m, 2H), 2.53-2.58(m, 1H), 2.61-2.64(dd, 1H), 2.71-2.76(m, 1H), 2.82-2.87(dd, 1H), 4.80-4.83(m, 1H), 6.76-6.76(m, 2H), 6.97-7.04(m, 3H), 7.12(d, 1H), 7.16-7.35(m, 12H); LRMS APCI m/z 535 [M+H]+
Example 20 5-tf3SV3-r(6-Hvdroxv-2-naDhthvl)oxvlPvrrolldln-1-vl)-S-m6thvl-2.2-dlphenvlhexanamlde
(Formula Removed)
Ammonium fluoride (27mg, 0.738mmol) was added to a solution of the product of preparation 19 (46mg, 0.0738mmol) in methanol (3mL) and water (O.SmL) and the mixture stirred at room temperature for 18 hours. The mixture was concentrated in vacuo and the residue purified using a RediSep® silica gel cartridge eluting with dichloromethane:methanol:0.88 ammonia (100:0:0 to 92:8:0.8). Appropriate fractions were concentrated In vacuo and the residue was dissolved in diethyl ether (30ml), washed with water (2 x 10ml), dried over magnesium sulphate and concentrated In vacuo to afford the title compound as an off-white foam in 35% yield, 14mg.
1HNMR(400MHz, CD3OD) 5: 0.97(s, 3H>, 1.06(s, 3H), 1.17-1.26(m, 2H), 1.88-1.98(m, 1H), 2.09-2.25(m, 1H), 2.33-2.51(m, 2H), 2.54-2.62(m, 1H), 2.63-2.68(m, 1H), 2.71-2.80(m, 1H), 2.81-2.91(m, 1H), 4.80-4.95(m, 1H), 6.89-7.00(m, 2H), 7.00-7.06(m, 2H), 7.10-7.26(m, 6H), 7.26-7.35(m, 4H), 7.47-7.54(m, 1H), 7.66-7.62(m, 1H); LRMS APCI m/z 509 [M+H]+
Example 21 5-K3S^3-f2-Hvdroxvphenoxv)Dvrrolldin-1-yl]-S-methvl-2.2-diphenvlhexanamide
(Formula Removed)
Dl-isopropylazodicarboxylate (0.22mL, 1.12mmol) was added to an ice-cooled solution of the product of preparation 17 (205mg, 0.56mmol), triphenyl phosphine (293mg, 1.12mmol), and 2-hydroxyphenol (616mg, 5.59mmoi) in tetrahydrofuran (4mL) the solution was stirred with Ice cooling for 2 hours. Triphenyl phosphine (293mg, 1.12mmol) and dl-isopropylazodlcarboxylate (0.22mL, 1.12mmol) were added and the resulting solution was stirred at room temperature for 16 hours. Di-isopropylazodicarboxylate (0.22mL, 1.12mmol) was added and the solution was stirred at room temperature for 4 hours. Tic analysis Indicated complete reaction: The reaction mixture was then concentrated In vacuo and the residue was purified using an (solute® SCX-2 cartridge, eluting with methanol followed by 1M ammonia in methanol. The basic fractions were evaporated under reduced pressure and the residue was purified by column chromatography on silica gel, eluting with pentane:(ethyl acetate:methanol:0.88 ammonia, 90:10:1) 1:0 to 1:1, to afford the title compound as a brown gum in 38% yield, 98mg.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 3H), 1.06(s, 3H), 1.25-1.29(m, 2H), 1.87-1.94(m, 1H), 2.03-2.11(m, 1H), 2.41-2.45(m, 2H), 2.51-2.57(m, 1H), 2.66-2.70(dd, 1H), 2.75-2.84(m, 2H), 4.80-4.85(m, 1H), 6.71-6.84(m, 4H), 7.21-7.37(m, 10H); LRMS APCI m/z459 [M+H]458 [M-
11
Example 22 5-[f3S)-3-f4-methoxvphenoxvbvrrolidin-1-yl]-5-methvl-2.2-diPhenvlhexanamlde
(Formula Removed)
Dl-isopropylazodicarboxylate (0.21 mL, 1.09mmol) was added to a solution of the product of preparation 17 (200mg, 0.546mmol), triphenyl phosphine (286mg, 1.09mmol), and 4-methoxyphenol (135mg, 1.09mmol) in tetrahydrofuran (3mL) the solution was stirred at room temperature for 16 hours. The reaction mixture was then concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 100:0 to 50:50 The product containing fractions were evaporated under reduced pressure and the residue was further purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:O.B8 ammonia, 100:0:0 to 95:5:0.5 to afford the title compound as a white foam in 14% yield, 36mg.
1HNMR(400MHz, CD3OD) 6: 0.96(s, 3H), 1.02(s, 3H), 1,19-1.25(m, 2H), 1.81-1.91(m, 1H), 2.00-2.11(m, 1H), 2.35-2.60(m, 4H), 2.66-2.72(m, 1H), 2.77-2.81(m, 1H), 3.73(s, 3H), 4.64-4.69(m, 1H), 6.72-6.81(m, 4H), 7.20-7.39(m, 10H); LRMS APCI m/z473 [M+H]+
\ Example 23
(Formula Removed)
5-[(3S)-3-(4-hvdroxvphenoxv)pvrrolid!n-1-vl-5-methvl-2.2-diphenvlhexanamide
Boron tribromide (1M in dlchloromethane, 0.76mL, 0.761mmol) was added to a solution of the product of example 22 (36mg, 0.076 1mmol) in dichloromethane (3mL) and the mixture was stirred at room temperature for 1 hour. Tic analysis indicated complete reaction. The reaction mixture was quenched via dropwlse addition of 0.88 ammonia (2mL) and stirred for 30 minutes to allow gas evolution. The reaction mixture was partitioned and aqueous was extracted with dichloromethane (2 x 5mL). Combined organic fractions were concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with ethyl acetate to 95:5:0.5 ethyl acetate:methanol:0.88 ammonia to afford the title compound as a white foam in 46% yield, 1 6mg.
1HNMR(400MHz, CD3OD) 5: 0.97(s, 3H), 1.03(s, 3H), 1.2Q-1.25(m, 2H), 1.81-1 .89(m, 1H), 2.01-2.09(m, 1H), 2.39-2.44(m, 2H), 2.51-2.61(m, 2H), 2.67-2.73(m, 1H), 2.77-2.81(m, 1H), 4.62-4.66(m, 1H), 6.63-6.69(m, 4H), 7.21-7.37(m, 10H); LRMS APCI m/z458 [M-1]'
Example 24 5-[(3S)3-(4-trifluromethvl-phenoxyl)pvrrolidin-1-vl]-5-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
Dl-isopropylazodlcarboxylate (0.11 ml, 0.546mmol) was added to a solution of the product of preparation 17 (100mg, 0.273mmol), trlphenyl phosphine (143mg, 0.546mmol), and 4-trifluromethylphenol (88mg, 0.546mmol) in tetrahydrofuran (3mL) the solution was stirred at room temperature for 4 hours. The reaction mixture was then concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with pentane:(ethyl acetate:methanol:0.88 ammonia, 90:10:1), 1:0 to 1:1 to afford the title compound as a white foam in 34% yield, 4Bmg.
1HNMR(400MHz, CD3OD) 5: 0.97(s, 3H), 1.03(s,,3H), 1.21-1.26(m, 2(H), 1.84-1.92(m, 1H), 2.11-2.20(m, 1H), 2i35-2.50(m, 2H), 2.52-2.62(m, 2H), 2.69-2.75(m, 1H), 2.85-2.89(m, 1H), 4.81-4.86(m, 1H), 6.93-6.96(d, 2H), 7.20-7.35(m, 10H), 7.52-7.54(d, 2H); LRMS APCI m/z ' 511[M+H]+510[M-1]
Example 25
(Formula Removed)
5-[(3m-3-(4-Trifluoromethvl-ph6noxy)pyrfoiidin-1-yl]-5-m6thvl-2.2dlahenvlhexanenltrlle
Sodium hydride (60% dispersion in mineral oil, 23mg, 0.574mmol) was added to an Ice-cooled solution of the product of preparation 20 (100mg, 0.287mmol) in N,N-dimethylformamide (1.5mL) and the mixture was stirred at 0°C for 30 minutes. 4-fluorobenzotrifluoride (71 mg, 0.431 mmol) in N,N-dimethylformamide (0.5mL) was added and the mixture was stirred for 16 hours, allowing the temperature to rise to 25°C. The solution was stirred at 50°C for 24 hours and then stirred at 25°C for 48 hours. Sodium hydride (60% dispersion in mineral oil, 23mg, 0.574mmol) was added and the solution was stirred for 1.25 hours at 50°C. The reaction mixture was then cooled to 25°C and quenched with water (8mL), concentrated in vacuo and the aqueous residue was partitioned between ethyl acetate (10mL) and water (10mL). The aqueous layer was separated and extracted with ethyl acetate (2x15mL). The combined organic solution was washed with brine (5mL), concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with pentane: ethyl acetate, 3:1 to 0:1, to afford the title compound as a colourless gum in 70% yield, 10mg.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 3H), 1.07(s, 3H), 1.44-1.48(m, 2H), 1.88-1.95(m, 1H), 2.16-2.25(m, 1H), 2.49-2.53(m, 2H), 2.56-2.62(m, 1H), 2.67-2.70(m, 1H), 2.75-2.80(q, 1H), 2.89-2.93(dd, 1H), 4.85-4.89(m, 1H), 6.96-6.98(d, 2H), 7.42-7.45(m, 10H), 7.53-7.55(d, 2H); LRMS APCI mlz 493 [M+H]+
Example 26 5-[(3R)-3-(4-trifluromethvl-phenoxvbvrrolldln-1-yl]-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
Potassium hydroxide (23mg, 0.406mmol) was added to a solution of example 25 (10mg, 0.0203mmol) in 3-methyl-3-pentanoI (2mL) and the mixture was heated under reflux for 16 hours. The solution was cooled to 25°C and potassium hydroxide (23mg, 0.406mmol) was added and the solution was heated under reflux for an additional 24 hours. The reaction mixture was then cooled to room temperature, concentrated in vacuo and the residue was
purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:0.88 ammonia, 95:5:0.5. to afford the title compound as a colourless gum in 68% yield, 7mg. 'HNMR)400MHz, CD3OD) 6: 0.97(s, 3H), 1.03(s, 3H), 1.20-1.25(m, 2H), 1.84-1.91 (m, 1H), 2.10-2.20(m, 1H), 2.34-2.49(m, 2H), 2.52-2.61(m, 2H), 2.69-2.74(m, 1H), 2.84-2.88(dd, 1H), 4.81-4.85(m, 1H), 6.94-6.96(d, 2H), 7.20-7.35(m, 10H), 7.53-7.55(d, 2H); LRMS APCI m/z 511 [M+H]+510[M-ir
Example 27 5-[(3m-3-(3-chlDro-4-methoxv-phenoxv)Pvrrolidin-1-yl]-5-methvl-2.2-dlphBnvlhexanenitrile
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 31 mg, 0.776mmol) was added to an ice-cooled solution of the product of preparation 20 (135mg, 0.388mmol) in N,N-dimethylformamide (4mL) and the mixture was stirred at 0°C for 15 minutes. 2-chloro-4-fluoro-anisole (93mg, 0.582mmol) in N,N-dimethylformamide (1mL) was added and the mixture was stirred for 16 hours, at 50°C. The solution was cooled to 25°C and sodium hydride (60% dispersion in mineral oil, 62mg, 1.55mmol) was added and the solution was stirred for 16 hours at 80°C. The reaction mixture was then cooled to 25°C and quenched with water (3mL), concentrated in vacuo and the aqueous residue was partitioned between ethyl acetate (20mL) and water (5mL). The aqueous layer was separated and extracted with ethyl acetate (2x20mL). The combined organic solution was washed with brine (10mL), concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with pentane:(ethyl acetate:methanol;0.88ammonia, 90:10:1), 3:1 to 1:1. The product containing fractions were evaporated under reduced pressure and the residue was further purified using an lsolute® SCX-2 cartridge, eluting with methanol followed by 1M ammonia in methanol. The basic fractions were evaporated to afford the title compound as a yellow gum in 32% yield, 61mg.
1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.08(s, 3H), 1.28-1.31(m, 2H), 1.76-1.80(m, 1H), 1.86-1.93(m, 1H), 2.09-2.18(m, 1H), 2.49-2.63(m, 2H), 2.67-2.70(m, 1H), 2.76-2.87(m, 2H), 3.80(s, 3H), 4.71-4.75(m, 1H), 6.74-6.77(dd, 1H), 6,89-6.95(dd, 1H), 7.24-7.46(m, 10H), 8.45-8.59(m, 1H); LRMS APCI m/z 489 [M+H]+
Example 28 5-[(3R)-3-(3-chloro-4-methoxy-phenoxv)pvrrolldin-1-yl]-5-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
Potassium hydroxide (140mg, 2.49mmol) was added to a solution of the product of example 27 (61mg, 0.125mmol) in 3-methyl-3-pentanol (5mL) and the mixture was heated under reflux for 16 hours. The solution was cooled to room temperature, concentrated in vacuo and the residue was partitioned between dichloromethane (10mL) and water (5mL), aqueous was extracted with dichloromethane (3 x 10mL): Combined organlcs were concentrated under reduced pressure and the residue purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:0.88 ammonia, 90:10:1. The product containing fractions were evaporated under reduced pressure to afford the title compound as a colourless gum In 33% yield, 21mg.
1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.09(s, 3H), 1.26-1.30(m, 2H), 1.88-1.96(m, 1H), 2.05-2.14(m, 1H), 2.35-2.49(m, 2H), 2.70-2.75(m, 2H), 2.82-2.88(m, 1H), 2.91-2.96(m, 1H), 3.81(s, 3H), 4.72-4.76(m, 1H), 6.73-6.76(dd, 1H), 6.88-6.89(d, 1H), 6.94-6.96(d, 1H), 7.24-7.36(m, 10H); LRMS APCI m/z 507 [M+H]+505 [M-1]
gxample 29
5-[(3S)-3-(3-Hvdroxv-5-methvl-phenoxv)-pvrrolidin-1-vl1-5-methvl-2.2-diphenvl-hexanoic acid amide
(Formula Removed)
Diisopropyl azodlcarboxylate (212µL, 1.093mmol) was added in three portions to an ice-cooled solution of triphenyl phosphine (287mg, 1.093mmol), 5-methylresorcinoI (678mg, 5.464mmol) and product from preparation 17 (200mg, 0.546mmol) in tetrahydrofuran (8mL) and the mixture was stirred at 0°C to room temperature for 2 hours. The reaction mixture was concentrated in vacuo and residue purified using an (solute® SCX-2 cartridge, eluting with methanol followed by 1M ammonia in methanol. Basic fractions were concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:0.88 ammonia, 98:2:0.2 to 94:6:0.6 to afford the title compound as a white foam in 27% yield. 70mg.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.06(8, 3H), 1.24-1.27(m, 2H), 1.87-1.93(m, 1H), 2.05-2.13(m, 1H), 2.19(s, 3H), 2.39-2.45(m, 2H), 2.61-2.69(m, 2H), 2.75-2.81(m, 1H), 2.85-
2.90(m, 1H), 4.69-4.73(m, 1H), 6.07(s, 1H), 6.13(s, 1H), 6.21(s, 1H), 7.21-7.35(m, 10H); LRMS ESI mlz 473 [M+H]+

Example30
5-[(3S)3-(3-Hydroxv-2-methvl-phenoxvVpvrrolldln-1-yl]-5-n
amide

liphenvl-hexanoic acid



(Formula Removed)
The title compound was prepared from the product of preparation 17 and 2-methylresorcinol,
using the same method as that described for example 29, to afford an off-white foam in 68%
yield.
1HNMR(400MHz, CD3OD) 5: 0.99(s, 3H), 1.04(s, 3H), 1.23-1.28(m, 2H), 1.86-1.93(m, 1H),
1.98(s, 3H), 2.02-2.11(m, 1H), 2.41-2.45(m, 2H), 2.57-2.67(m, 2H), 2.71-2.78(m, 1H), 2.88-
2.92(m, 1H), 4.69-4.72(m, 1H), 6.26-6.28(d, 1H), 6.38-6.40(d, 1H), 6.87-6.91(t, 1H), 7.21-
7.24(m, 2H), 7.27-7.30(t, 4H), 7.34-7.36(m, 4H); LRMS ESI mlz 473 [M+H]+
Example 31
S-[(3S)-3-f2.4-Dlchloro-5-Hvdroxy-phenoxv)-pvrrolidin-1-yl]-5-methyl^2.2-dlphenvl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 17 and 4,6-dichlororesorcinol using the same method as that described for example 29, with the addition of further triphenyl phosphine (2eq) and diisopropyl azodicarboxylate (2eq) after both 18hrs and 24hrs, and subsequent stirring for an additional 24hrs, to afford an off-white foam In 21% yield.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.06(s, 3H), 1.24-1.280m, 2H), 1.89-1.96(m, 1H), 2.05-2.14(m, 1H), 2.38-2.49(m, 2H), 2.59-2.70(m, 2H), 2.75-2.81(m, 1H), 2.89-2.93(m, 1H), 4.71-4.74(m, 1H), 6.48 (s, 1H), 7.21-7.24(m, 3H), 7.26-7.31(t, 4H), 7.34-7.37(m, 4H); LRMS APCI m/z 527 [M+H]+

Example 32 6-[(3S)--3-(4.5-Dlchloro-2-Hvdroxv-phenoxy)-pvrrolidln-1-vl]-5-methvl-2.2-diphenvl-hexanoic
acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 17 and 4,5-
dlchlorocatechol, using the same method as that described for example 29, with the addition
of further triphenyl phosphine (2eq) and dfisopropyl azodicarboxylate (2eq) after both 18hrs
and 24hrs, and subsequent stirring for an additional 24hrs, to afford an off-white foam in 18%
yield. . .
1HNMR(400MHz, CD3OD) 6: 1.03(s, 3H), 1.09(8, 3H), 1.19-1.31(m, 2H), 1.90-1.97(m, 1H), 2.05-2.14(m, 1H), 2.34-2.49(m, 2H), 2.61-2.67(m, 1H), 2.69-2.73(m, 1H) 2.76-2.79(m, 1H), 2.86-2.92(m, 1H), 4.78-4.83(m, 1H), 6.85 (s, 1H), 6.94(s, 1H), 7.21-7.40(m, 10H); LRMS ESI m/z
Example 33
5-[(3S)-3-(3-Chloro-5-methoxy-phenoxy)-pvrrolidin-1-vl]-5-methvl-2.2-dlphenvl-hexanolc acid amide
(Formula Removed)
Diisopropyl azodicarboxylate (160µL, 0.820mmol) was added In three portions to an ice-cooled solution of triphenyl phosphine (215mg, 0.820mmol), 3-chloro-5-methoxyphenol (325mg, 2.049mmol) and the product from preparation 17 (150mg , 0.410mmol) in tetrahydrofuran (8mL) and the mixture was stirred at 0°C to room temperature for 18 hours. The reaction mixture was concentrated in vacuo and purified using an (solute® SCX-2 cartridge, eluting with methanol, then with 2M ammonia in methanol. Basic fractions were concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88ammonla, 98:2:0.2 to 94:6:0.6 to afford the title compound as a green gum In 97% yield, 200mg.
1HNMR(400MHz, CD3OD) 5: 0.97(s, 3H), 1.03(s, 3H), 1.20-1.25(m, 2H), 1.81-1.89(m, 1H), 2.06-2.14(m, 1H), 2.35-2.49(m, 2H), 2.51-2.60(m, 2H), 2.67-2.73(m, 1H), 2.79-2.83(m, 1H),
3.75(3, 3H), 4.70-4.74(m, 1H), 6.29-6.30(t, 1H), 6.41-6.42(t, 1H), 6.51-6.52(t, 1H), 7.20-7.24(m, 2H), 7.26-7.30(t, 4H), 7.33-7.35(m, 4H); LRMS ESI m/z 507 [M+H]+
Example 34
5-[(3S)-3-(3-ChlorQ-5-hvdroxv-phenoxv)-pvrrolidln-1-yl]-5-methvl-2.2-dlphenvl-hexanolc acid amide
(Formula Removed)
Boron tribromlde (1M In dichloromethane, 1.97mL, 1.976mmol) was added to an ice-cooled solution of the product of example 33 (200mg, 0.395mmol) in dichloromethane (10mL) and the mixture was stirred at 0°C to room temperature for 18 hours. The reaction was quenched with 0.88 ammonia solution and stirred at room temperature for 90 minutes. The reaction mixture was extracted with dichloromethane (3x10mL) and the combined organic solution was dried over sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, afforded the title compound as a white foam in 45% yield, 88mg.
1HNMR(400MHz, CD3OD) 5: 1.01(s, 3H), 1.06(s, 3H), 1.24-1.28(m, 2H), 1.85-1.93(m, 1H), 2.06-2.15(m, 1H), 2.38-2.46(m, 2H), 2.61-2.69(m, 2H), 2.74-2.81(m, 1H), 2.87-2.92(m, 1H),' 4.70-4.74(m, 1H), 6.18-6.19(t, 1H), 6.30-6.31(t, 1.H), 6.38-6.39(t, 1H), 7.22-7.26(m, 2H), 7.28-7.31 (t, 4H), 7.33-7.36(m, 4H); LRMS ESI m/z 493 [M+H]+
Example 35
5-[(3S)3-[4-Chloro-2-Methoxv-phenoxv)-Pvrrolidln-1-vl1-5-methyl-2.2-diphenvl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product, of preparation 17 and 4-chloro-2-methoxyphenol, using the same method as that described for example 33, with stirring for 2hrs and Isolate® SCX cartridge purification to afford a colourless gum in 100% yield. 1HNMR(400MHz, CD3OD) 5: 0.96(s, 3H), 1.02(s, 3H), 1.21-1.25(m, 2H), 1.83-1.90(m, 1H), 2.02-2.11(m, 1H), 2.42-2.46(m, 2H), 2.48-2.54(m, 1H), 2.62-2.66(dd, 1H), 2.69-2.80(m, 2H),
3.73(s, 3H), 4.68-4.73(m, 1H), 6.75-6.77(d, 1H), 6.82-6.8S(dd, 1H), 6.91-6.92(d, 1H), 7.20-7.23(m, 2H), 7.26-7.29(t, 4H), 7.33-7.37(m, 4H); LRMS ESI m/z 473 [M+H]+
Example 36 5-ff3SV3-(4-Chloro-2-Hvdroxv-phenoxvVpvrroHdln-1-yl]-S-methvl-2.2-diphenvl-hexanolc acid
(Formula Removed)
The title compound was prepared from the product of example 35, using the same method as that described for example 34, with stirring for 3 hours and purification by column chromatography on silica gel, eluting with ethyl acetate:methanol:ammonia, 98:2:0.2 to 94:6:0.6 to afford a white foam In 72% yield.
1HNMR(400MHz, CD3OD) 5: 0.96(s, 3H), 1.02(s, 3H), 1.21-1.25(m,2H), 1.83-1.90(m, 1H), 2.02-2.11(m, 1H), 2.42-2.46(m, 2H), 2.48-2.54(m, 1H), 2.62-2.66(dd, 1H), 2.69-2.80(m, 2H), 4.68-4.73(m, 1H), 6.75-6.77(d, 1H), 6.82-6.85(dd, 1H), 6.91-6.92(d, 1H), 7.20-7.23(m, 2H), 7.26-7.29(t, 4H), 7.33-7.37(m, 4H); LRMS ESI m/z 473 [M+H]+
Example 37
5-[(3S)-3-(2-Chloro-3-Methoxv-phenoxv)-Pvrrolldln-1-vl]-6-rnethyl-2.2-dlphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 17 and the product of preparation 21, using the same method as that described for example 33, with Isolate® SCX cartridge purification to afford a white foam in 100% yield.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.04(s, 3H), 1.23-1.28(m, 2H), 1.88-1.95(m, 1H), 2.04-2.13(m, 1H), 2.42-2.46(m, 2H), 2.56-2.63(m, 1H), 2.65-2.70(m, 1H), 2.72-2.79(m, 1H), .2.88-2.93(m, 1H), 3.85(s, 3H), 4.79-4.81(m, 1H), 6.54-6.57(dd, 1H), 6.67-6.69(dd, 1H), 7.14-7.18(t, 1H) 7.20-7.24(m, 2H), 7.27-7.30(t, 4H), 7.33-7.37(m, 4H); LRMS ESI m/z 507 [M+H]+
Example 38
5-[(3S)-3-(2-Chloro-3-Hvdroxv-phenoxy)-pyrrolidin-1-yl]-5-methvl-2,2-dlphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 37, using the same method as that described for example 34, to afford a white foam in 37% yield.
1HNMR(400MHz, CD3OD) 6: 1.08(s, 3H), 1.12(s, 3H), 1.31-1.36(m, 2H), 1.97-2.05(m, 1H), 2.07-2.16(m, 1H), 2.44-2.48(m, 2H), 2.77-2.96(m, 3H), 3.05-3.10(q, 1H), 4.82-4.87(m, 1H), 6.43-6.45(dd, 1H), 6.54-6.57(dd, 1H), 7.01-7.05{t, 1H), 7.22-7.26(m, 2H), 7.29-7.33(t, 4H), 7.36-7.39(m, 4H); LRMS ESI m/z 493 [M+H]+
Example 39 & 40
The following compounds were prepared from the product of preparation 17 and 2-chlororesorcinol, using the same method as that described for example 33, with the addition of further triphenyl phosphine (2eq) and diisopropyl azodicarboxylate (2eq) after 18hrs,-and subsequent stirring for an additional 3hrs. Crude material was purified by column chromatography on silica gel, eluting with ethyl acetate: methanol:0.88ammonia, 98:2:0.2 to 94:6:0.6, to yield a mixture of regioisomers that were separated by HPLC on a Luna C8(2) acidic column, eluting with acetonitrile:water:diethylamine, 1:1:0.05 to afford the title compounds as white solids in 12% and 1% yield respectively.
Example 39
5.rf3S)-3-(4-Chloro-3-Hvdroxv-phenoxy)-pvrrolidln-1-yl]-5-methvl-2.2-dlphenyl-hexanoic acid amide
(Formula Removed)
1HNMR(400MHz, CD3OD) 5: 0.98(s, 3H), 1.04(s, 3H), 1.23-1.27(q, 2H), 1.87-1.95(m, 1H), 2.05-2.13(m, 1H), 2.41-2.47(m, 2H), 2.54-2.60(m, 1H), 2.62-2.66(dd, 1H), 2.71-2.77(q, 1H), 2.86-2.90(q, 1H), 4.69-4.74(m, 1H), 6.32-6.36(m, 2H), 7.07-7.09(d, 1H), 7.20-7.24(m 2H), 7.27-7.30(t, 4H), 7.35-7.37(m, 4H); LRMS ESI m/z 493 [M+H]+
Example 40
5-[(3S)3-(2-Chloro-5-Hvdroxv-phenoxvVDvrrolldln-l-yl]-5.methvl-2.2-diDhBnvl-liexanoio acid amide
(Formula Removed)
1HNMR(400MHz, CD3OD) 5: 0.99(3, 3H), 1.04(s, 3H), 1.21-1.26(m, 2H), 1.82-1.90(01, 1H), 2.05-2.15(m, 1H), 2.35-2.46(m, 2H), 2.53-2.62(m, 2H), 2.69-2.75(q, 1H), 2.81-2.86(q, 1H), 4.66-4.71(m, 1H), 6.27-6.30(dd, 1H), 6.39-6.40(d, 1H), 7.09-7.11(d, 1H), 7.21-7.3B(m, 10H); LRMS ESI m/z 493 [M+H]+
Example 41 5-K3RV3-(3-Chloro-2-Methoxv-phenoxvVpvrrolidin-1-yl]-5-methvl-2.2-dlphenvl-hexanenltrile
(Formula Removed)
The product of preparation 20 (150mg, 0.431 mmol) In dimethylformamide (3ml) was added drop wise to an Ice-cooled solution of sodium hydride (60% dispersion in mineral oil, 52mg, 1.293mmol) In dimethylformamide (1ml). After stirring for 1 hour the product of preparation 22 (103mg, 0.646mmol) In dimethylformamide (1ml) was added and the mixture was heated to 60°c for 96 hours. The solution was concentrated In vacuo and partitioned between ethyl acetate (10ml) and water (10ml). The organic layer was extracted and washed again with water (10ml), then dried over sodium sulphate and concentrated in vacuo, to afford the title compound as a brown oil in 74% yield, 156mg.
1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.08(s, 3H), 1.44-1.49(m, 2H), 1.90-1.97(01, 1H), 2.12-2.21 (m, 1H), 2.50-2.62(m, 3H), 2.74-2.83(m, 2H), 2.87-2.91 (m, 1H), 3.74(s, 3H), 4.81-4.84(m, 1H), 6.83-6.85(dd, 1H), 6.93-7.00(m, 2H), 7.25-7.42(m, 10H); LEWIS ESI m/z 489
Example 42
5-[(3R^-3-f3-Chloro-2-Methoxv-PhenoxvVpvrrolldln-1-yl]-5-methvl-2.2-diphenvl-h6xanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 41, using the same method as that described for example 2. The crude compound was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, to afford a white foam, in 50% yield.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.05(s, 3H), 1.23-1.27(q, 2H), 1.88-1.96(m, 1H), 2.07-2.16(m, 1H), 2.41-2.46(m, 2H), 2.56-2.61(m, 1H), 2.64-2.77(m, 2H), 2.86-2.92(m, 1H), 3.75(s, 3H), 4.77-4.82(m, 1H), 6.80-6.83(dd, 1H), 6.96-6.99(m, 2H), 7.21-7.25(m, 2H), 7.27-7.31 (t, 4H), 7.34-7.36(m, 4H); LRMS ESI m/z 507 [M+H]+*
Example 43
5-[(3R)-3-f3-Chlpro-2-Hvdroxv-phenoxyVDvrrolldin-1-yl]-5-methvl-2,2-diphenyl-hexanolc acid amide
(Formula Removed)
The title compound was-prepared from the product of example 42, using the same method as that described for example 34, to afford a white foam in 65% yield.
1HNMR(400MHz, CD3OD) 6: 1.05(s, 3H), 1.09(s, 3H), 1.28-1.32(m, 2H), 1:89-1.98(m, 1H), 2.03-2.13(m, 1H), 2.42-2.46(m, 2H), 2.59-2.67(m, 1H), 2.70-2.75(m, 1H), 2.81-2.93(m, 2H), 4.84-4.88(m, 1H), 6.66-6.70(1, 1H), 6.77-6.79(d, 1H), 6.88-6.91 (d, 1H), 7.21-7.25(m, 2H), 7.28-7.32(t, 4H), 7.35-7.37(m, 4H); LRMS ESI m/z 493 [M+H]+
Example 44
5-[(3S)3-(3-Hydroxv-2.5-dimethvl-PhenoxyVpvrrolidin-1-yl]-5-methvl-2.2-diphenvl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 17 and 2,5-dimethylresorcinol, using the same method as that described for example 29, with the addition of further triphenyl phosphine (2eq) and diisopropyl azodicarboxylate (2eq) after 18hrs, and subsequent stirring for 1 hour to afford a pale brown foam in 58% yield. 1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.04(s, 3H), 1.24-1,28(m, 2H), 1.85-1.92(m, 1H), 1.93(s, 3H), 2.0l-2.10(m, 1H), 2.20(s, 3H), 2.41-2.45(m, 2H), 2.56-2.66(m, 2H), 2.70-2.78(m, 1H), 2.86-2.93(m, 1H), 4.67-4.873(m, 1H), 6.11(s, 1H), 6.24(s, 1H), 7.20-7.24(m, 2H), 7.26-7.30(t, 4H), 7.33-7.37(m, 4H); LRMS APCI m/z487 [M+H]+
Example 45 5-[(3S)3-(3-Fluoro-5-Methoxv-PhenoxvVpvrrolidln-1-yl]-S-methvl-2.2-diphenvl-hexanoic acid
(Formula Removed)
The title compound was prepared from the product of preparation 17 and the product of preparation 23, using the same method as that described for example 33, to afford the product as a colourless gum In 100% yield. LRMS ESI m/z 491 [M+H]+
Example 46
5-[(3S)-3-(3-Fluoro-5-Hvdroxy-phenoxv^-Pvrrolidin-1-yl]-5-methvl-2.2-diphenvl-hexanoic acjd amide
(Formula Removed)
The title compound was prepared from the product of example 45, using the same method as that described for example 34, with the addition of further boron tribromide (1M in dichloromethane, 4eq) after 3 hours, and subsequent stirring for 2hrs. Crude material was purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:0.88 ammonia, 98:2:0.2 to 94:6:0.6 to afford a white foam in 35% yield.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.04(s, 3H), 1.21-1.26(m, 2H), 1.82-1.90(m, 1H), 2.05-2.14(m, 1H), 2.39-2.45(m, 2H), 2.54-2.63(m, 2H), 2.69-2.75(m, 1H), 2.82-2.87(q, 1H),
4.66-4.71(m, 1H), 6.02-6.11(m, 3H), 7.21-7.26(m, 2H), 7.27-7.31(t, 4H), 7.33-7.36(m, 4H); LRMS APCI m/z 477 [M+H]+
Example 47
5-[phenoxvVpvrrolidin-1-yl]-5-methvl-2.2-diphenvl-
hexanenitrile

(Formula Removed)
The title compound was prepared from the product of preparation 20 and the product of preparation 24, using the same method as that described for example 41. The residue was purified by column chromatography on silica gel, elutlng with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, to afford a pale brown gum in 32% yield.
1HNMR(400MHz, CD3OD) 5: 1.03(s, 3H), 1.08(s, 3H), 1.44-1.48(m, 2H), 1.87-1.90(m, 1H), 2.14-2.22(m, 1H), 2.49-2.54(m, 2H), 2.56-2.62(m, 1H), 2.67-2.70(d, 1H), 2.75-2.81(q, 1H), 2.87-2.91(m, 1H), 3.80(s, 3H), 4.82-4.85(m, 1H), 6.61(s, 1H), 8.67(s, 1H), 6.74 (s, 1H), 7.24-7.42(m, 10H); LRMS APCI m/z 523 [M+H]+
Example 48
5-[f3R)-3-f3-Methoxv-5-trlfluoromethvl-phenoxv)-pvrrolidln-1-yl]-5-methvl-2.2-dlphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 47, using the same method as that described for example 2, to afford product a colourless gum in 83% yield. 1HNMR(400MHz, CD3OD) 5: 0.98(s, 3H), 1.02(s, 3H), 1.20-1.25(m, 2H), 1.82-1.89(m, 1H), 2.08-2.17(m, 1H), 2.39-2.46(m, 2H), 2.49-2.59(m, 2H), 2.66-2.72(q, 1H), 2.81-2.86(m, 1H), 3.80(s, 3H), 4.76-4.81{m, 1H), 6.58-6.60(q, 1H), 6.64(s, 1H), 6.74(s, '1H), 7.18-7.36(m, 10H); LRMS APCI m/z 541 [M+H]+
Example 49 5-[(3RV3-(3-Hvdroxv-5-trifluoromethvl-phenoxv)-DvrrQlidin-1-yl]-5-methvl-2.2-diphenvl-
hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 48, using the same method as that described for example 34, to afford a colourless gum in 40% yield. 1HNMR(400MHz, CD3OD) 5: 0.99(s, 3H), 1.04(s, 3H), 1.22-1.27(m, 2H), 1.84-1.91 (m, 1H), 2.08-2.16(m, 1H), 2.38-2.47(m, 2H), 2.54-2.63(m, 2H), 2.69-2.75(q, 1H), 2.85-2.89(m, 1H), 4.73-4.78(m, 1H), 6.45-6.47(t, 1H), 6.52-6.53(8, 1H), 6.60-6.61(8, 1H), 7.21-7.24(m, 2H), 7.27-7.30(t, 4H), 7.34-7.36(m, 4H); LRMS APCI mlz 527 [M+H]+*
Example 50
5-[(3S)-3-f4-Fluoro-3-Methoxv-Phenoxy)-PViTolldin-1-vl1-S-methvl-2.2-dlphenvl-hexanolc acid
amide •
(Formula Removed)
The title compound was prepared from the product of preparation 17 and the product of preparation 25, using the same method as that described for example 33, with the addition of further triphenyl phosphine (2eq) and diisopropyl azodicarboxylate (2eq) after both 16hrs and 17hrs, with subsequent stirring for an additional 1hr and Isolute® SCX cartridge purification to afford a pale brown foam In 86% yield.
1HNMR(400MHz, CD3OD) 6: 0.98(s, 3H), 1.03(s, 3H), 1.21-1.26(m, 2H), 1.82-1.89(m, 1H), 2.04-2.13(m, 1H), 2.37-2.47(m, 2H), 2.52-2.62(m, 2H), 2!68-2.74(q, 1H), 2.81-2.85(m, 1H), 3.79(8, 3H), 4.69-4.73(m, 1H), 6.28-6.32(m, 1H), 6.52-6.56(dd, 1H), 6.90-6.95(dd, 1H), 7.20-7.24(m, 2H), 7.26-7.30(t, 4H), 7.33-7.36(m, 4H); LRMS APCI mlz 491 [M+H]+
Example 51
5-[(3S)3-(2-Fluoro-3-Methoxv-phenoxy)-pvrrolldln-1-yl]-5-methvl-2.2-diphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 17 and the product of preparation 26, using the same method as that described for example 33, with the addition of further triphenyl phosphine (2eq) and diisopropyl azodicarboxylate (2eq) after both 16hrs and 17hrs, with subsequent stirring for an additional 1hr and (solute0 SCX cartridge purification to afford a pale yellow foam in 86% yield.
1HNMR(400MHz, CD3OD) 6: 0.98(s, 3H), 1.02(s, 3H), 1 .22-1 .26(m, 2H), 1.85-1.93(m, 1H), 2.04-2. 12(m, 1H), 2.40-2.45{m, 2H), 2.51-2.56(m, 1H), 2.62-2.65(m, 1H), 2.68-2.74(q, 1H), 2.82-2.86(m, 1H), 3.83(s, 3H), 4.74-4.78(m, 1H), 6.53-6.57(t, 1H), 6.66-6.70(t, 1H), 6.93-6.98(td, 1H), 7.20-7.24(m, 2H), 7.27-7.30(t, 4H), 7.33-7.36(m, 4H); LRMS APCI m/z 491
Example 52
5-[f3S)-3-(4-Fluoro-3-Hvdroxv-phenoxvVpvrrolidln-1-Yn-5-methvl-2.2-diphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 50, using the same method as that described for example 34, with stirring for 3 hours and purification by column chromatography on silica gel, elutlng with ethyl acetate:methanol:0.88 ammonia, 98:2:0.2 to 94:6:0.6. to afford a white foam in 52% yield.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.04(s, 3H), 1.22-1.27(m, 2H), 1.82-1.90(m, 1H), 2.03-2.12(m, 1H), 2.38-2.46(m, 2H), 2.55-2.64(m, 2H), 2.70-2.76(q, 1H), 2.83-2.87(m, 1H), 4.6-4.69(m, 1H), 6.19-6.23(dt, 1H), 6.38-6.40(dd, 1H), 6.85-6.90(dd, 1H), 7.21-7.25(m, 2H), 7.27-7.31 (t, 4H), 7.33-7.36(m, 4H); LRMS APCI m/z 477 [M+H]+
Example 53
S-K3S)-3-(2-Fluoro-3-Hvdroxv-phenoxv)-pyrrolldln-1-yl]-5-methvl-2.2-diphenvl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product of example 51 , using the same method as that described for example 34, with stirring for 3 hours and purification by column chromatography on silica gel, eluting with ethyl acetate:methanol:ammonia, 98:2:0.2 to 94:6:0.6 to afford a white foam in 26% yield.
1HNMR(400MHz, CD3OD) 5: 1.00 (s, 3H), 1.04(s, 3H), 1 .24-1 .28(m, 2H), 1.88-1.95(m, 1H), 2.04-2.13(m, 1H), 2.41-2.47(m, 2H), 2.55-2.63(rh, 1H), 2.66-2.71(m, 1H), 2.72-2.78(q, 1H), 2.86-2.91 (m, 1H), 4.73-4.77(m, 1H), 6.38-6.42(t, 1H), 6.48-6.53(t, 1H), 6.80-6.85(td, 1H), 7.21-7.25(m, 2H), 7.27-7.31(4, 4H), 7.34-7.37(m, 4H); LRMS ESI m/z 477 [M+H]+
Example 54 5-[f3RV3-(3-Hvdroxv-benzvloxv)-Pvrrolidin-1-vl1-5-methvl-2.2-dlphenvl-hexanolc acid amide
(Formula Removed)
4M Hydrochloric acid in dioxane (3ml) and water (0.3ml) were added to the product of preparation 29 (95mg, 0.186mmol) and the resulting solution was stirred at 60°c for 20 minutes. The reaction was cooled to room temperature and partitioned between ethyl acetate (20ml) and saturated sodium hydrogen carbonate solution (10ml). The aqueous layer was extracted and washed with ethyl acetate (2x1 Oml) and the combined organic layers dried over sodium sulphate and concentrated In vacuo. The residue was purified by column chromatography, eluting with ethyl acetate:methanol:0.88 ammonia, 97:3:0.2 to 95:5:0.5, to afford the title compound as a colourless gum in 51% yield, 44mg.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.00(s, 3H), 1.24-1.28(m, 2H), 1.74-1.81 (m, 1H), 1.87-1.94(111, 1H), 2.40-2.44(m, 2H), 2.49-2.58(m, 2H), 2.61-2.67(m, 1H), 2.71-2.76(m, 1H), 3.98-4.03(m, 1H), 4.36(s, 2H), 6.67-6.69(d, 1H), 6.74-6.76(m, 2H), 7.09-7.13(t, 1H), 7.22-7.26(m, 2H), 7.29-7.32(1,4H), 7.35-7.38(m, 4H); LRMS ESI m/z 473 [M+H]+*
Example 55 5-l(3S)-3-f(3-Bromobenzvnoxvlpyrrolidin-1-vl>-5-methv-2.2-dlphenvlhexanenitrile
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 150mg, 3.74mmoi) was added portionwise to an ice-cooled solution of the product of preparation 18 (1.3g, 3.74mmol) in N,N-dimethylformamide (20mL) and the mixture was stirred at 0°C for 1 hour. 3-Bromobenzylbromide (935mg, 3.74mmol) was added and the mixture was stirred for 4 hours, allowing the temperature to rise to 25°C. The reaction mixture was then quenched with water, concentrated in vacuo and the aqueous residue was partitioned between ethyl acetate (50mL) and water (30mL). The aqueous layer was separated and extracted with ethyl acetate (4x30mL). The combined organic solution was dried over sodium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with pentaneiethyl acetate, 50:50 to 100:0, to afford the title compound as a pale brown oil in 70% yield.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 3H), 1.04(s, 3H), 1.41-1.54('m, 2H), 1.77-1.85(m, 1H), 1.93-2.02(tn, 1H), 2.49-2.54(m, 3H), 2.62-2.76(m, 3H), 4.02-4.07(m, 1H), 4.43(m, 2H), 7.18-7.50(m, 14H); LRMS APCI m/z 518 [M+H]+
Example 56
5-ff3SV3-r(3'-Hydroxvbiphenyl-3-vnmethoxv1pvrrolldln-1-vl)-5-methyl-2.2-
dlphenvlhexanenltrile
(Formula Removed)
[1,1'-Bis(diphenylphosphino)ferrocene]palladium(ll) chloride (16mg, 19ymol) was added to a solution of the product of example 55 (205mg, 0.38mmol), 3-hydroxyphenylboronic acid (106mg, 0.77mmol) and sodium carbonate (81 mg, 0.77mmol) in tetrahydrofuran (5mL) and water (1mL) and the mixture was heated under reflux for 16 hours. The cooled reaction mixture was then concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with ethyl acetate:methanol, 98:2 to 96:4, to afford the title compound In 25% yield, 51 mg.
1HNMR(CD3OD, 400MHz) 5: 1.04(s, 3H), 1.06(s, 3H), 1.46-1.52(m, 2H), 1.82-1.90(m, 1H), 1.96-2.03(m, 1H), 2.50-2.55(m, 3H), 2.67-2.80(m, 3H), 4.08-4.13(m, 1H), 4.52(s, 2H),
6.76(dd, 1H), 7.01(m, 1H), 7.05(d, 1H), 7.20-7.24(m, 1H), 7.27-7.42(m, 12H), 7.48(d, 7.54(s, 1H); LRMS ESI m/z 529[M-H]'
Example 57 5-[(3S)3-(Biphenvl-3-vlmethQxv^pvrrolidin-1-yl]-5-methvl-2.2-diphenvlhexanenitrile
(Formula Removed)
The title compound was prepared from the product of example 55 and benzeneboronic acid, using the same method as that described for example 56, as a green gum. in 54% yield. 1HNMR(400MHz, CD3OD) 6: 1.11(s, 3H), 1.13(s, 3H), 1.51-1.68(m, 2H), 1.94-2.03(m, 2H), 2.52-2.56(m, 2H), 2.70-2.77(m, 1H), 2.82-2.93(m, 3H), 4.08-4.13 & 4.13-4.18(2xm, 1H), 4.45 & 4.54 (2xm, 2H), 7.26-7.43(m, 19H); LRMSAPCI m/z 516 [M+H]+
Example 58
5-(3S)3-[(2'-Hvdroxvbiphenvl-3-vnmethoxv1pvrrolidin-1-vl}-5-methvl-2.2-
diphenvlhexanenltrile
(Formula Removed)
The title compound was prepared from the product of example 55 and 2-hydroxyphenylboronic acid, using the same method as that described for example 56. The crude compound was purified by column chromatography on silica gel, eluting with ethyl acetate followed by dichloromethaneimethanol, 95:5, to afford the desired product as pale brown foam in 61 % yield.
1HNMR(CD3OD, 400MHz) 5: 1.03(s, 3H), 1.07(s, 3H), 1.47-1.53(m, 2H), 1.83-1.90(m, 1H), 1.94-2.03(m, 1H), 2.50-2.55(m, 2H), 2.57-2.64(m, 1H), 2.69-2.83(m, 3H), 4.09-4.14(m, 1H), 4.51(s, 2H), 6.85-6.89{m, 2H), 7.14(m, 1H), 7.20-7.46(m, 14H), 7.51 (s, 1H); LRMS ESI m/z 529[M-Hr
Example 59 5-((3S)3-rf4-Bromobenzvnoxvlpvrrolidln-1-vl}-S-methvl-2.2-diphenvlhexanenitrile
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 35mg, O.88mmol) was added portionwise to an ice-cooled solution of the product of preparation 18 (205mg, 0.59mmol) in N,N-dimethylformamide (5mL) and the mixture was stirred for 1 hour. 4-Bromobenzylbromide (220mg, O.88mmol) was added and the mixture was stirred for 3 hours, allowing the temperature to rise to 25°C. The reaction mixture was then re-cooled to 0°C, further sodium hydride (60% dispersion in mineral oil, 220mg, O.88mmol) was added and the mixture was stirred at room temperature. After 18 hours, the mixture was re-cooled to 0°C and sodium hydride (60% dispersion In mineral oil, 293mg, 1.17mmol) was added. After stirring for 1 hour, further 4-bromobenzylbromide (220mg, 0.88mmol) was added and the mixture was stirred for 3 hours at room temperature. The reaction mixture was then quenched with water, concentrated in vacuo and the aqueous residue was partitioned between ethyl acetate (50mL) and water (30mL). The organic layer was separated, dried over sodium sulfate, concentrated in vacuo and the residue purified using an Isolute® SCX-2 cartridge, eluting with methanol followed by 0.5M ammonia in methanol. The basic fractions were evaporated under reduced pressure and the residue further purified by column chromatography on silica gel, eluting with dichloromethane: methanol:0.88 ammonia, 95:5:5 to afford the title compound as a pale orange gum.
1HNMR(400MHz, CD3OD) 5: 1.02(s, 3H), 1.05(s, 3H), 1.40-!53(m, 2H), 1.77-1.85(m, 1H), 1.93-2.02(m, 1H), 2.50-2.55(m, 3H), 2.64-2.78(m, 3H), 4.03-4.08(m, 1H), 4.42(s, 2H), 7.23(d, 2H), 7.28-7.44(m, 12H); LRMS APCI m/z 519 [M+H]+
Example 60
5-((3S)-3-r(3'-Hydroxvblphenyl-4-vl^methoxv]Dvrrolidln-1-vl}-5-methyl-2.2-
djphenvlhexanenitrlle
(Formula Removed)
1,1'-Bis(diphenylphosphino)ferrocene]palladlum(ll) chloride (12mg, 14umol) was added to a solution of the product of example 59 (150mg, 0.29mmol}, 3-hydroxyphenylboronic acid (80mg, 0.58mmol) and sodium carbonate (62mg, 0.58mmol) In tetrahydrofuran .(5.5mL) and

(Formula Removed)
water (1mL) and the mixture was heated under reflux for 18 hours. Further 1,1'-bis(diphenylphosphino)ferrocene]palladium(ll) chloride (12mg, 14umol) was added and the mixture was heated under reflux for 6 hours before cooling to room temperature. The reaction mixture was then concentrated In vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 95:5:0.5, to afford the title compound as a pale brown foam in 47% yield, 73mg, LRMS ESI m/z 531 [M+H]+
Example 61 5-[(3S)-3-r(3'-Hvdroxvbiphenvl-3-vl)methoxylpvrrolidln-1-yl}-5-methyl-2.2-diPhenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 56, using the same method as that described for example 2, as a colourless gum in 17% yield.
1HNMR(400MHz; CD3OD) 5: 1.22(s, 3H), 1.24(s, 3H), 1.42-1.47(m, 2H), 1.96-2.06(m, 1H), 2.11-2.19(m, 1H), 2.42-2.47(m, 2H), 3.14-3.23(m, 4H), 4.23-4.27(m, 1H), 4.56(m, 2H), 6.76-6.79(dd, 1H), 7.02(m, 1H), 7.06(d, 1H), 7.23-7.41(m, 13H), 7.49-7.51(d, 1H), 7.54(s, 1H); LRMS ESI m/z 549 [M+H]+
Example 62
S-((3S)-3-ff4'-HvdroxybiPhenvl-3-vnmethoxvlDvrrolld!n-1-vl}-5-methyl-2.2-
diphenvlhexanenitrlle
(Formula Removed)
The title compound was prepared from the product of example 55 and 4-hydroxyphenylboronic acid, using the same method as that described for example 56. The crude compound was purified by column chromatography on silica gel, eluting with ethyl acetate. The appropriate fractions were evaporated under reduced pressure and the residue was further purified by column chromatography on silica gel, eluting with dichtoromethane:methanol:0.88 ammonia, 98:2:0.2 to 95:5:0.5, to afford the desired compound as a pale brown gum in 78% yield.
1HNMR(CDaOD, 400MHz) 5: 1.03(s, 3H), 1.06(s, 3H), 1.46-1.52(m, 2H), 1.80-1.88(m, 1H), 1.93-2.02(m, 1H), 2.49-2.60(m, 3H), 2.66-2.80(m, 3H), 4.04-4.09(m, 1H), 4.44(s, 2H), 6.80(d, 2H), 7.26-7.43(m, 15H), 7.50(s, 1H); LRMS ESI m/z 529[M-H]
Example 63 5-((3S)3-[(4'-Hvdroxvblphenvl-3-vl)methoxvlPvrrolldin-1-vll-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 62, using the same method as that described for example 2, In 6% yield.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.Q2(s, 3H), 1.25-1,29(m, 2H), 1.78-1.87(m, 1H), 1.88-1.99(m, 1H), 2.40-2,44(m, 2H), 2.52-2.59(m, 1H), 2.60-2.71(m, 2H), 2.72-2.78(m, 1H), 4.03-4.08(m, 1H). 4.48(s, 2H), 6.84(d, 2H), 7.20-7.38(m, 12H), 7.41-7.45(m, 3H), 7,48(s, 1H); LRMS ESI m/z 549 [M+H]+
Example 64 S-f(3S)3-[(2'-Hvdroxvbiphenvl-3-vnmethoxvlpvrrolidin-1-vl)-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 58, using the same method as that described for example 2. The crude was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 90:10:1 to 80:20:2, to afford the desired product as a white solid in 21 % yield.
1HNMR(400MHz, CD3OD) 5: 0.98(s, 3H), 1.00(s, 3H), 1.23-1.27(m, 2H), 1.75-1.84(m, 1H), 1.88-1.98(m, 1H), 2.39-2.44(m, 2H), 2.47-2.66(m, 3H). 2.71-2.75(m, 1H), 4.02-4.08(m, 1H), 4.47(s, 2H), 6.86-6.89(m, 2H), 7.12-7.16(m, 1H), 7.20-7.37(m, 13H), 7.44(d, 1H), 7.49(s, 1H); LRMS ESI m/z 549 [M+H]+
Example 65, 5-l(3S)3-r(3'-Hvdroxvblphenvl-4-vl)methoxy]pvrrolldin-1-vl)-5-methvl-2.2-dlphenvlhexanamlde
(Formula Removed)
The title compound was prepared from the product of example 60, using the same method as that described for example 2. The crude was purified by column chromatography on silica gel, elutlng with dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 90:10:1, to afford the desired product as a white solid in 28% yield.
1HNMR(400MHz, CD3OD) 6: 1.03(s, 3H), 1.05(s, 3H), 1.27-1.31(m, 1H), 1.52-1.56(m, 1H), 1.81-1.89(m, 1H), 1.90-2.00(m, 1H), 2.34-2.38(m, 1H), 2.41-2.45(m, 2H), 2.59-2.64(m, 1H), 2.67-2.76(m, 1H), 2.79-2.83(m, 1H), 4,04-4.1 0(m, 1H), 4.47(m, 2H), 6.75(d, 1H), 7.01 (m, 1H), 7.05(d, 1H), 7.18-7 .38(m, 11H), 7.43(d, 2H), 7.53(d, 2H); LRMS ESI m/z 549 [M+H]+
Example 66 5>f(3S)-3-fBiphenvl-3-vlmethoxv)pvrrolidin-1-yl]-5-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
The title compound was prepared from the product of example 57, using the same method as that described for example 2, as a brown gum in 23% yield.
1HNMR(400MHz, CD3OD) 5: 1.18(s, 3H), 1.20(s, 3H), 1.38-1.44(m, 2H), 1.97-2.04(m, 1H), 2.05-2.12(m, 1H), 2.41-2.46(m, 2H), 3.03-3.14(m, 4H), 4.21-4.24(m, 1H), 4.56(m, 2H), 7.23-7.44(m, 16H), 7.50-7.55(m, 1H), 7.57-7.60(m, 2H); LRMS APCI m/z 533 [M+H]+*
Example 67 5-[f3R)-3-(4-Fluoro-3-hvdroxv-benzvloxv)-Dvrrolidln-1-yl]-5-methvl-2,2-dlphenvlhexanamldB
(Formula Removed)
Hydrochloric acid in dioxane (4M, 4ml) and water (0.5ml) were added to the product of preparation 34 (150mg, 0.248mmol) and the resulting solution refluxed for 45 minutes. The solvent was removed In vacua and the residue partitioned between ethyl acetate (10ml) and saturated sodium hydrogen carbonate solution (3ml). The aqueous layer was separated and extracted with further ethyl acetate (2x1 Oml). The combined organic layers were washed with water (5ml), brine (5ml), dried over sodium sulphate and concentrated In vacua. The residue was purified by column chromatography, eluting with dichloromethane:methanol:0.88 ammonia (95:5:0.5 to 93:7:0.7 to 90:10:1) to afford the title compound as an off-white foam in 44% yield, 54mg.
1HNMR(400MHz, CD3OD) 6: 1.05(s, 3H), 1.06(s, 3H), 1.28-1.33(m, 2H), 1.81-1.97(m, 2H), 2.41-2.45(m, 2H), 2.63-2.86(m, 4H), 4.02-4.07(m, 1H), 4.34(s, 2H), 6.70-6.74(m, 1H), 6.87-6.90(dd, 1H), 6.94-6.99(dd, 1H), 7.23-7.38(m, 10H); LRMS ESI m/z491 [M+H]+
Example 68 5-[(3S)3-(3-Cvano-5-hvdroxv-phenoxv)-pvrrolldln-1-yl]-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
Ammonium formate (33mg, 0.523mmol) and 20% Pd(OH)2\C (3mg) were added to a solution of the product of preparation 36 (30mg, 0.0523mmol) in ethanol (2mL) and the mixture refluxed for 15 minutes. The reaction mixture was then filtered through Arbocel* and the filtrate was concentrated In vacua. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88ammonia (95:5:0.5) to afford the title compound as a yellow foam in 87% yield, 22mg.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.04(s, 3H), 1.23-1.28(m, 2H), 1.84-1.93(m, 1H), 2.08-2.17(m, 1H), 2.36-2.50(m, 2H), 2.56-2.63(m, 2H), 2.71-2.77(q, 1H), 2.85-2.89(m, 1H), 4.73-4.79(m, 1H), 6.53-6.54(d, 1H), 6.60-6.61 (d, 1H), 6.66-6.67(d, 1H), 7.22-7.36(m, 10H); LRMS ESI m/z 484 [M+H]+
Example 6.9. 5-ff3SV3-(2-Cvano-5-methoxv-phenoxv^-Dvrrolldin-1-yl]-5-methvl-2.2-dtohenvlhexanamlde
(Formula Removed)
The title compound was prepared from the product of preparation 17 and 2-hydroxy-4-methoxybenzonitrile using the same method as that described for preparation 36, to afford an orange foam in 36% yield.
'HNMR^OOMHz, CD3OD) 6: 1.00(s, 3H), 1.04(8, 3H), 1.21-1.29(m, 2H), 1.89-1.98(m, 1H), 2.10-2.20(m, 1H), 2.35-2.51 (m, 2H), 2.57-2.68(m, 2H), 2.73-2.83(m, 1H), 2.91-2.99(m, 1H), 3.86(8, 3H), 4.88-4.91(m, 1H), 6.51(d, 1H), 6.61-6.64(dd, 1H), 7.20-7.39(m, 10H), 7.48-7.50 (d, 1H); LRWIS ESI m/z 498 [M+H]+
Example 70 5-lf3SV3-r(7-Hvdroxv-2-naDhthvnoxvlPvrrolldin-1-vl>-5-methvl-2.2-dlPhenvlhexanamlde
(Formula Removed)
Ammonium fluoride (53mg, 1.44mmol) was added to a solution of the product of preparation 37 (90mg, 0.144mmol) In methanol (3mL) and water (0.3mL) and the mixture was heated at 50°C for 18 hours. The mixture was concentrated In vacua and the residue purified using a RediSep® silica gel cartridge elutlng with dichloromethane:methanol:0.88 ammonia (100:0:0 to 90:10:1). Appropriate .fractions were concentrated In vacua and the residue further purified using a .RediSep® silica gel cartridge eluting with dichloromethane:methanol:0.88 ammonia (100:0:0 to 93:7:0.7) to afford the title compound as a colourless gum in 6% yield, 4.5mg. 1HNMR(400MHz, CD3OD) 5: 0.96(s, 3H), 1.06(s, 3H), 1.19-1.30(m, 2H), 1.88-1.98(m, 1H), 2.11-2.23(m, 1H), 2.34-2.52(m, 2H), 2.54-2.64(m, 1H), 2.64-2.68(m, 1H), 2.72-2.82(m, 1H), 2.85-2.91 (m, 1H), 4.82-4.89(m, 1H), 6.77-6.83(m, 1H), 6.85-6.87(m, 1H), 6.88-6.91 (m, 1H), 6.98-7.01 (m, 1H), 7.15-7.35(111,10H), 7.54-7.62(m, 2H); LRWIS APCI m/z 509 [M+H]+
Example 71 5-K3SV-3-f4-Phenvlphenoxv)Dvrrolidln.1-yl]-5-methyl-2.2-diphenvlhexanamide

(Formula Removed)


A solution of trlphenylphosphlne (143mg, 0.546mmol) In tetrahydrofuran (1mL) and di-isopropylazodicarboxylate (0.11 ml, 0.546mmol) were added to a solution of the product of preparation 17 (100mg, 0.273mmol) in tetrahydrofuran (1mL) and the mixture was stirred at room temperature for 15 minutes. 4-Phenylphenol (93mg, 0.546mmol) was added and the mixture was stirred at room temperature for 18 hours. Further triphenylphosphlne (143mg, 0.646mmol) and di-lsopropylazodicarboxylate (0.11 ml, 0.546mmol) were added and the solution was stirred at room temperature for 72 hours. The mixture was concentrated In vacua and the residue purified by column chromatography on silica gel, eluting with dichloromethaneimethanol (100:0 to 95:5) to afford the title compound as a colourless oil in 28% yield, 40mg.
1HNMR(400MHz, CD3OD) 6: 0.99(s, 3H), 1.07(s, 3H), 1.23-1.26(m, 2H), 1.90-1.98(m, 1H), 2.10-2.19(m, 1H), 2.39-2.46(m, 2H), 2.58-2788(m, 2H), 2.75-2.89(m, 2H), 4.80-4.84(m, 1H), 6.88-6.90(d, 2H), 7.20-7.41 (m, 13H), 7.49-7.56(dd, 4H); LRMS APCI m/z 519 [M+H]+
Example 72 5-ff3R)-3-f3-chloro-4-hvdroxvphenoxv)Dvrrolldin-1-yl]-5-methvl-2.2-diphenvlhexanamide

(Formula Removed)


Boron tribromlde (1M in dichloromethane, 0.16mL, 0.158rnmol) was added to a solution of the product of example 28 (20mg, 0.039mmol) in dichloromethane (3mL) and the mixture was stirred at room temperature for 72 hours. The reaction mixture was quenched via dropwise addition of 0.88 ammonia (5mL) and stirred for 24 hours. The aqueous layer was separated and extracted with dichloromethane (3 x 20mL). The combined organic layers were concentrated in vacua and the residue was purified by column chromatography on silica gel, eluting with ethyl acetate:methanol:0.88ammonia (100:0:0 to 95:5:0.5) to afford a colourless gum. This was further purified by HPLC using a Curosil PFP-Acid 150*21.2 stationary phase, eluting with 0.1% Formic acid (aq):(acetonitrile + 0.1% Formic acid), 95:5 to 0:100. Appropriate fractions were concentrated in vacua and the residue was partitioned between dichloromethane (15ml) and water (5ml), and the aqueous layer was separated and extracted with, further dichloromethane (2 x 15ml). The combined organic layers were washed with sodium hydroxide solution (1M, 5ml), brine (10ml) and concentrated in vacua. The residue

was further purified by preparative thin layer chromatography eluting with dichloromethane:methanol:0,88ammonia (90:10:1). Clean product bands were washed from the silica gel using dlchloromethane:methanol:0.88ammonia (95:5:0.5), filtered and concentrated in vacua to afford the title compound as a colourless gum in 16% yield, 3mg. 1HNMR(400MHz, CD3OD) 5: 1.18(s, 3H), 1.22(s, 3H), 1.28-1.30(m, 2H), 1.39-1.44(m, 2H), 2.08-2.14(m, 2H), 2.42-2.47(m, 2H), 3.04-3.27(m, 2H), 4.82-4.87(m, 1H), 6.66-6.70(m, 1H), 6.82-6.87(m, 2H), 7.25-7.38(m, 10H); LRMS APCI m/z 493 [M+H]491
Example 73 S-[(3R)-3-(3-FluQro-5-methoxv-phenoxy)-pvrrolldln-1-yl]-5-methvl-2.2-dlphenvlhexanamlde
(Formula Removed)
Diisopropyl azodicarboxylate (160uL, 0.822mmol) was added in three portions to an Ice-cooled solution of triphenyl phosphine (215mg, 0.822mmol), the product of preparation 23 (175mg, 1.232mmol) and the product of preparation 16 (150mg, 0.411mmol) in tetrahydrofuran (7mL) and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated in vacuo and residue purified using art (solute® SCX-2 cartridge, eluting with methanol followed by 2M ammonia In methanol. Basic fractions were concentrated in vacuo to afford the title compound as a pale brown foam in 75% yield, 150mg.
1HNWIR(400MHz, CD3OD) 5: 0.98(s, 3H), 1.03(s, 3H), 1.21-1.26(m, 2H), 1.81-1.89(m, 1H), 2.06-2.15(m, 1H), 2.38-2.46(m, 2H), 2.50-2.61(m, 2H), 2.67-2.72(m, 1H), 2.78-2.85(m, 1H), 3.74(s, 3H), 4.69-4.74(m, 1H), 6.14-6.19(m, 2H), 6.24-6.28(m, 1H), 7.21-7.36(m, 10H); LRMS ESI m/z 491 [M+H]+
Example 74 6-[(3R)-3-(3-Fluoro-5-hydroxy-j3lienoxy)-Dyrrolldln-1-yl1-5-methvl-2.2-diPhenvl-hexanamide
(Formula Removed)
Boron trlbromide (1M in dichloromethane, 1.2mL, 1.224mmol) was added to an ice-cooled solution of the product of example 73 (150mg, 0.306mmol) In dichloromethane (4mL) and the mixture was stirred at room temperature for 18 hours. The reaction was quenched with 0.88
ammonia solution and stirred at room temperature for 2 hours. The reaction mixture was adjusted to pH 8 by dropwise addition of 2N hydrochloric acid (aq) and extracted with dichloromethane (3x1 OmL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica ge), eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, afforded the title compound as a pale brown foam in 49% yield, 71 mg.
1HNMR(400MHz, CD3OD) 5: 1.01(s, 3H), 1.06(8, 3H), 1.24-1 .28(m, 2H), 1.85-1.92(m, 1H), 2.07-2.16(111, 1H), 2.40-2.45(m, 2H), 2.59-2.67(m, 2H), 2.73-2.79(q, 1H), 2.87-2.91(m, 1H), 4.68-4.72(m, 1H), 6.03-6.12(m, 3H), 7.21-7.26(m, 2H), 7.28-7.32(m, 4H), 7.33-7.37(m, 4H); LRMS ESI m/z 477 [M+H]+, 475 [M-H]'
Example 75 5-[(3RV3-(2-Fluoro-3-methoxv-phenoxvVpvrrolldln-1-yl]-5-methvl-2.2-diphenvlhexanamid6
(Formula Removed)
Diisopropyl azodicarboxylate (160uL, 0.822mmol) was added'in three portions to an ice-cooled solution of triphenyl phosphine (215mg, 0.822mmol), the product of preparation 26 (160mg, 1.127mmol) and product from preparation 16 (150mg, 0.411mmol) in tetrahydrofuran (7mL) and the mixture was stirred at 0°C to room temperature for 16 hours. Additional triphenyl phosphine (215mg, 0.822mmol) and dilsopropyl azodicarboxylate (160uL, 0.822mmol) were added and the mixture stirred for a further 48 hours. The reaction mixture was concentrated In vacuo and the residue purified using an Isolate® SCX-2 cartridge, eluting with methanol followed by 2M ammonia in methanol. Basic fractions were concentrated In vacuo to afford the title compound as a pale brown foam in 75% yield, 145mg. LRMS ESI m/z 491 [M+H]+
Boron tribromide (1M in dichloromethane, 1.1 ml, 1.224mmol) was added to an ice-cooled solution of the product of example 75 (140mg, 0.286mmol) in dichloromethane (4mL) and the
(Formula Removed)
Example 76 5-[3R)-3-(2-Fluoro-3-hvdroxv-phenoxv)-Dvrrolidin-1-yl]-5-[nethvl-2.2-diphenvlhexanamlde
mixture was stirred at room temperature for 2 hours. The reaction was quenched with 0.88 ammonia solution and stirred at room temperature for 16 hours. The reaction mixture was adjusted to pH 8 by dropwise addition of 2N hydrochloric acid (aq) and extracted with dichloromethane (2x1 OmL). The combined organic layers were dried over sodium sulfate and concentrated In vacuo. Purification of the residue by column chromatography on silica gel, eluting,with dichloromethane:methanol:0.88 ammonia, 95:5:0.5, afforded the title compound as a pale yellow foam in 15% yield, 20mg.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.04(s, 3H), 1.26-1.28(01, 2H), 1.85-1.93(m, 1H), 2.06-2.12(rn, 1H), 2.42-2.46(m, 2H), 2.54-2.60(m, 1H), 2.65-2.75(m, 2H), 2.85-2.90(q, 1H), 4.74-4.78(m, 1H), 6.38-6.42(1, 1H), 6.49-6.53(t, 1H), 6.80-6.85(t, 1H), 7.22-7.25(m, 2H), 7.28-7.32(m, 4H), 7.35-7.38(m, 4H); LRMS ESI m/z 477 [M+H]475 [M-H]'
Example 77 5-[f3R\-3-^2-Chloro-3-m6thoxv-phenQxvVpvrrolidln-1-yl]-5-methvl-2.2-diPhenvlhexanamide
(Formula Removed)
Diisopropyl azodicarboxylate (118uL, 0.606mmol) was added in three portions to an ice-cooled solution of triphenyl phosphine (160mg, 0.606mmol), the product of preparation 21 (120mg, 0.757mmol) and product from preparation 16 (111mg, 0.411mmol) in tetrahydrofuran (7mL) and the mixture was stirred at 0°C to room temperature for 3 hours. Additional triphenyl phosphine (160mg, 0.606mmol), and diisopropyl azodicarboxylate (118uL, 0.606mmol) were added and the mixture stirred for a further 16 hours. The reaction mixture was concentrated In vacuo and residue purified using an (solute® SCX-2 cartridge, eluting with methanol followed by 2M ammonia in methanol. Basic fractions were concentrated in vacuo to afford the title compound as a pale brown foam In 82% yield, 124mg.
1HNMR(400MHz, CD3OD) 6: 1.00(s, 3H), 1.05(s, 3H), 1.24-1.29(m, 2H), 1.85-1.97(m, 1H), 2.05-2.15(m, 1H), 2.43-2.47(m, 2H), 2.58-2.64(m, 1H), 2.66-2.72(m, 1H), 2.73-2.80(m, 1H), 2.89-2.95(m, 1H), 3.85(s, 3H), 4.79-4.81(m, 1H), 6.55-6.57(d, 1H), 6.67-6.70(d, 1H), 7.15-7.19(t, 1H), 7.21-7.24(m, 2H), 7.27-7.31 (m, 4H), 7.34-7.38(m, 4H); LRMS ESI m/z 507 [M+H]+
Example 78 5-[(3RV3-(2-Chloro-3-hvdroxv-phenQxv)-Dvrrolldin-1-yl]-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 77, using the same method as that described for example 74, to afford a pale orange foam in 36% yield. 1HNMR(400MHz, CD3OD) 6: 1.03(8, 3H), 1.07(s, 3H), 1.27-1.32(m, 2H), 1.92-1 .99(m, 1H), 2.06-2.14(m, 1H), 2.43-2.47(m, 2H), 2.65-2.71(m, 1H), 2.74-2.78(d, 1H), 2.80-2.86(q, 1H), 2.96-3.00(m, 1H), 4.79-4.82(m, 1H), 6.41-6.43(dd, 1H), 6.53,6.55(dd, 1H), 7.00-7.04(t, 1H), 7.21-7.25(m, 2H), 7.28-7.32(m, 4H), 7.36-7.39(m, 4H); LRMS ESI m/z 493 [M+H]491 [M-H]
Example 79 5-[(3R>-3-f4-Chloro-3-hvdroxv-benzvloxv)-Dvrrolidin-1-yl]-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
Hydrochloric acid (4M in dioxan, 4ml) and water (0.5ml) were added to the product of preparation 44 (161mg, 0.295mmol) and the mixture was heated under reflux for 30 minutes. The reaction mixture was then cooled to room temperature and partitioned between ethyl acetate (20mL) and saturated aqueous sodium hydrogen carbonate solution (20mL). The aqueous layer was separated, extracted with further ethyl acetate (20mL) and the combined organic layers were dried over sodium sulfate and concentrated in vacua. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 90:10:1, to afford the title compound as a pale brown foam In 19% yield, 29mg.
1HNMR(400MHz, CD3OD) 6:'1.01(8, 3H), 1.02(s, 3H), 1.24-1.28(m, 2H), 1.75-1.82(m, 1H), 1.87-1.94(m, 1H), 2.40-2.44(m, 2H), 2.51-2.60(m, 2H), 2.63-2.69(q, 1H), 2.73-2.77(q, 1H), 3.98-4.03(m, 1H), 4.34(s, 2H), 6.70-6.73(dd,- 1H), 6.87-6.88(d, 1H), 7.18-7.21(d, 1H), 7.22-7.26(m, 2H), 7.29-7.33(m, 4H), 7.35-7.38(m, 4H); LRMS APCI m/z 505 [M-H]'
Example 80 6-rf3R)-3-f3-methoxv-4-chloro-phenoxv)pvrroHdln-1-yl]-5-methvl-2,2-diphenvlhexanenitrlle
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 60mg, 1.466mmol) was added to an Ice-cooled solution of the product of preparation 20 (I70mg, 0.489mmol) in N,N-dimethylformamlde (5mL) and the mixture was stirred at 0°C for 30 minutes. 2-chloro-5-fluoro-anisole (73ul, 0.586mmol) was added and the mixture was stirred for 18 hours at room temperature. The mixture was then heated at 60°C for 6 hours. The mixture was cooled to room temperature, further sodium hydride (60% dispersion in mineral oil, 60mg, 1.466mmol) was added and heating continued at 60°C for .18 hours. The solution was cooled to 0°C, further sodium hydride (60% dispersion in mineral oil, 100mg, 2.443mmol) was added and the solution stirred for 30 minutes. Additional 2-chloro-5-fluoro-anisole (122ul, 0.977mmol) was added and mixture heated at 80°C for 18 hours. The reaction mixture was then cooled to room temperature, quenched with water (3mL), concentrated in vacua and the aqueous residue was partitioned between ethyl acetate (10mL) and water (5mL). The aqueous layer was separated and extracted with further ethyl acetate (2x1 OmL). The combined organic layers were washed with brine (10mL), dried over sodium sulfate, concentrated In vacua and the residue was purified by column chromatography on silica gel, eluting with ethyl acetate:methanol :0.88ammonia, 99:1:0.1, to afford the title compound as a colourless gum in 34% yield, 80mg.
1HNMR(400MHz, CD3OD) 6: 1.03(s, 3H), 1.08(s, 3H), 1.44-1.49(m, 2H), 1.88-1.95(m, 1H), 2.12-2.21(m, 1H), 2.49-2.54(m, 2H), 2.56-2.62(m, 1H), 2.68-2.70(d, 1H), 2.76-2.82(m, 1H), 2.85-2.89(m, 1H), 3.80(s, 3H), 4.79-4.81(m, 1H), 6.39-6.42(d, 1H), 6.54(s, 1H), 7.16-7.20(d, 1H), 7.26-7.42(m, 10H); LRMS APCI m/z 489 [M+H]+
Example 81 5-[(3R)-3-(3-methoxv-4-chl6ro-phenoxvVpvrrolidin-1-yl]-5-methvl-2.2-dlphenvlhexanamlde
(Formula Removed)
Potassium hydroxide (185mg, 3.275mmol) was added to a solution of the product of example 80 (80mg, 0.163mmol) in 3-methyl-3-pentanol (3mL) and the mixture was heated under reflux for 24 hours. Further potassium hydroxide (93mg, l.638mmol) was added and mixture heated
at reflux for a further 5 hours. The reaction mixture was then cooled to room temperature, concentrated In vacua and the residue was partitioned between ethyl acetate (15mL) and water (10mL). The aqueous layer was separated, extracted with further ethyl acetate (15mL) and the combined organic layers were dried over sodium sulfate and concentrated In, vacua. The residua was purified by column chromatography in. dichloromethane:methanol:0.88 ammonia, 97:3:0.3 to 94:6:0,6, to afford the title compound as a white foam in 64% yield, 53mg.
1HNMR(400MHz, CD3OD) 6: 0.98(s, 3H), 1,05(s, 3H), 1.20-1.26(m, 2H), 1.84-1.93(m, 1H), 2.07-2.16(m, 1H), 2.34-2.49(m, 2H), 2.53-2.65(m, 2H), 2.70-2.77(m, 1H), 2.81-2.88(m, 1H), 3.80(s, 3H), 4.74-4.79(m, 1H), 6.36-6.38(dd, 1H), 6.51-6.52(d, 1H), 7.18-7.20(d, 1H), 7.21-7.35(m, 10H); LRMS APCI m/z 507 [M+H]+
Example 82 5-[f3RV3-(3-hvdroxv-4-chloro-phenoxvVpvrrolidln-1-yl]-5-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
Boron tribromide (1M in dichloromethane, 0.4mL, 0.4mmol) was added to an ice-cooled solution of the product of example 81 (50mg, 0.099mmol) In dichloromethane (2mL) and the mixture was stirred at'room temperature for 18 hours. Further boron tribromide (1M In dichloromethane, 0.2mL, Q.2mmol) was added and the mixture stirred at room temperature for a further 3 hours. The reaction was quenched with 0.88 ammonia solution and stirred at room temperature for 1 hour. The reaction mixture was acidified to pH 6 by dropwise addition of 2N hydrochloric acid (aq) and extracted with dichloromethane (2x1 Oml). The combined organic layers were dried over sodium sulfate and concentrated In vacua. Purification of the residue by column chromatography on silica gel, elutlng with dichloromethane:methanol:0.88 ammonia, 97:3:0.3 to 94:6:0.6, afforded the title compound as a white foam in 70% yield, 34mg.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.06(s, 3H), 1.24-1.28(m, 2H), 1.83-1.93(m, 1H), 2.06-2.15(m, 1H), 2.35-2.47(m, 2H), 2.60-2.68(m, 2H), 2.74-2.81(m, 1H), 2.87-2.91(m, 1H), 4.68-4.73(m, 1H), 6.28-6.31(dd, 1H). 6.40-6.41(d, 1H), 7.10-7.12(d, 1H), 7.22-7.35(m, 10H); LRMS ESI m/z 493 [M+H]491 [M-H]
Example 83 'S-r(3RV3-f3-hvdroxv-4-cvano-phenoxy^-pvrroHdin-1-vl1-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
Ammonium formate (44mg, 0.698mmol) and palladium hydroxide (20% on carbon, 8mg) were added to a solution of the product of preparation 45 (40mg, 0.070mmol) in ethanol (2mL) and the mixture was stirred at reflux for 20 minutes. The reaction was cooledr the catalyst removed by filtration over Arbocel® and the filtrate concentrated In vacua. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 90:10:1, afforded the title compound as a white foam in 55% yield, 18mg.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 3H), 1.06(s, 3H), 1.24-1.28(m, 2H), 1.87-1.94(m, 1H), 2.09-2.18(m, 1H), 2.35-2.49(m, 2H), 2.61-2.71(m, 2H), 2.75-2.82(q, 1H), 2.91-2.95(q, 1H), 4.76-4.79(m, 1H), 6.32-6.35(m, 2H), 7.21-7.36(m, 11H); LRMS APCI m/z484 [M+H]+
Example 84, 5-[(3S)3-(3-methoxv-benzvloxv)Dvrrolldin-1-yl]-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 26mg, 0.638mmol) was added to an ice-cooled solution of the product of preparation 18 (185mg, 0.532mmol) in N,N-dimethylformamide (5mL) and the mixture was stirred at 0°C for 60 minutes. 3-Methoxybenzyl bromide (128mg, 0.638mmol) was added and the mixture was stirred for 3 hours at room temperature. Additional 3-methoxybenzyl bromide (160mg, 0.797mmol) was added and the mixture stirred for a further 2 hours. The reaction mixture was quenched with water (3m L), concentrated in vacua and the aqueous residue was partitioned between ethyl acetate (20mL) and water (10mL), The aqueous layer was separated and extracted with further ethyl acetate (2x1 OmL). The combined organic layers were concentrated in vacua and the residue was purified by column chromatography on silica gel, eluting with dichloromethane to afford a colourless oil, 180mg.
Potassium hydroxide (430mg, 7.692mmol) was added to a solution of this colourless oil (180mg, 0.385mmol) in 3-methylr3-pentanol (5mL) and the mixture was heated under reflux for 24 hours. The reaction mixture was cooled to room temperature, concentrated In vacua and the residue was partitioned between ethyl acetate (20mL) and water (10mL). The aqueous layer was separated, extracted with further ethyl acetate (10mL) and the combined organic layers were dried over sodium sulfate and concentrated In vacua. The residue was purified by column chromatographyi eluting initially with pentane, then dlchloromethane: methanol:0.88 ammonia, 95:5:0.6 up to 90:10:1, to afford the title compound as a white foam in 16% yield, 40mg.
1HNMR(400MHz, CD3OD) 5: 1.01(s, 3H), 1.03(s, 3H), 1.26-1.30(m, 2H), 1.77-1.85(m, 1H), 1.88-1.95(m, 1H), 2.40-2.45(m, 2H), 2.53-2.72(m, 3H), 2.75-2.79(m, 1H), 3.76(s, 3H), 4.00-4.05(m, 1H), 4.41(s, 2H), 6.80-6.83(d, 1H), 6.86-6.88(m, 2H), 7.16-7.37(m, 11H); LRMS ESI m/z487[M+H]+
Example 85 5-[(3RV3-(2-ChlQro-3-hVdroxv-benzvloxvVpvrrolld (Formula Removed)
The title compound was prepared from the product of preparation 49, using the same method
as that described for example 79, to afford a white foam in 34% yield.
1HNMR(400MHz, CD3OD) 6: 1.11 (a, 3H), 1.13(s, 3H), 1.34-1.38(m, 2H), 1.90-2.02(m, 2H),
2.41-2.45(m, 2H), 2.83-3.02(m, 4H), 4.14-4.18(m, 1H), 4.49-4.57(m, 2H), 6.84-6.87(dd, 1H),
6.91-6.93(d, 1H), 7.06-7.10(t,1H), 7.24-7.27(m, 2H), 7.30-7.38(m, 8H); LRMS APCI m/Z 505
[M-H]-
Example 86 5-Methvl-5-(4-phenoxvDlDerldin-1-yl]-2.2-dlphenvlhexanenitrlle
(Formula Removed)
A solution of the product of preparation 50 (9.03g, 21mmol) in tetrahydrofuran (270mL) was cooled to -20°C. Zirconium tetrachloride (9.91 g, 43mmol) was added and the reaction mixture was stirred at -20°C for 1 hour. Methyl magnesium chloride (3M in tetrahydrofuran, 63.8mL, 191mmol) was then added dropwlse and the mixture was stirred for 1 hour, with the temperature maintained below -10°C. The reaction was quenched with ethanol (20mL), concentrated in vacuo and the residue was partitioned between 2N sodium hydroxide solution (200mL) and ethyl acetate (250mL). The aqueous layer was separated and extracted with ethyl acetate (2x200mL), and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with pentaneiethyl acetate, 75:25 to 67:33. The appropriate fractions were evaporated under reduced pressure and the residue was further purified by using an (solute® SCX-2 cartridge, methanol followed by 1M ammonia in methanol, to afford the title compound as a yellow gum in a 41 % yield (3.83g).
1HNMR(400MHz, CDCI3) 6: 1.04(s, 6H), 1.54-1.58(m, ,2H), 1.71-1 .B0(m, 2H), 1.99-2.02(m, 2H), 2.25(m, 2H), 2.53-2.57(m, 2H), 2.70-2.75(m, 2H), 4.22-4.28(m, 1H), 6.92-6.96(m, 3H), 7.28-7.32(m, 4H), 7.35-7.39(m, 4H), 7.45-7.47(m, 4H); LRWIS APCI m/z 439 [M+H]+
Example 87 5-{4-K3-Bromobenzvl)oxvlpiperldin-1-vl)-S-methvl-2,2-diprtenvlhexanenitrlle
(Formula Removed)
The title compound was prepared from the product of preparation 53, using the same method as that described for example 86, as a yellow gum in 33% yield.
1HNMR(400MHz, CDCI3) 5: 0.98(s, 6H), 1.46-1.60(m, 4H), 1.88-1.91 (m, 2H), 2.04-2.09(m, 2H), 2.46-2.50(m, 2H), 2.65-2.68(m, 2H), 3.28-3.34(m, 1H), 4.50(s, 2H), 7.18-7.42(m, 13H). 7.51 (s, 1H); LRMS ESI m/z 533 [M+H]+
Example 88 5-(4-ff3-Hvdroxybenzynoxv1piperidln-1-yl)-5-methvl-2.2-dlphenvlhexanenltrile
(Formula Removed)
n-Butyl lithium (2.5M in hexanes, 0.18mL, 0.45mmol) was added dropwise to a solution of the product of example 87 (200mg, 0.38mmol) in tetrahydrofuran (5mL), cooled to -78°C, and the mixture was stirred for 15 minutes. Trimethylborate (0.13mL, 1.13mmol) was added and the mixture was stirred at -78°C for 30 minutes and at room temperature for 2 hours. 4-methylmorpholine N-oxide (132mg, 1.13mmol) was added and the mixture was heated under reflux for 4 hours and stirred at room temperature for 18 hours. The reaction mixture was then partitioned between ethyl acetate (30mL) and water (30mL) and the organic layer was separated and washed with water (20mL). The organic solution was dried over sodium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 90:10:1. The appropriate fractions were evaporated under reduced pressure and the residue was further purified by preparative tic, eluting with dichloromethane:methanol:0.88 ammonia, 90:10:1, to afford the title compound as a gum in 3% yield, 5mg.
1HNMR(400MHz, CD3OD) 6: 1.02(s, 6H), 1.46-1.58(m, 4H), 1.86-1.90(m, 2H), 2.13-2.19(m, 2H), 2.49-2.53(m, 2H), 2.70-2.75(m,-2H), 3.33-3.39(m, 1H), 4.45(s, 2H), 6.67-6.70(m, 1H), 6.77-6.79(m, 2H), 7.12(m, 1H), 7.28-7.43(m, 10H); LRMS ESI m/z 469 [M+H]+
Example 89 5-[4-(Benzvloxvtoiperidin-1-yl]-5-methvl-2,2-diphenvlhexanenltrile
(Formula Removed)
n-Butyl lithium (2.5M in hexanes, 0.23mL, 0.56mmol) was added dropwise to a solution of the product of example 87 (200mg, 0.38mmol) in tetrahydrofuran (8mL), cooled to -78°C, and the mixture was stirred for 30 minutes. Carbon dioxide was then passed through the solution, with stirring at -78°C, for 3.5 hours before the mixture was allowed to warm to room temperature. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate (30mL) and water (20mL). The organic layer was separated, washed with water, dried over magnesium sulfate and concentrated In vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 98:2:0.2, afforded the title compound as a by-product, as an off white solid in 68% yield, 116mg.
1HNMR(400MHz, CD3OD) 5: 1.00(s, 6H), 1.45-1.49(m, 2H), 1.50-1.58(m, 2H), 1.86-1.90(m, 2H), 2.11-2.17(m, 2H), 2.48-2.53(m, 2H), 2.69-2.72(m, 2H), 3.33-3.39(m, 1H), 4.51(s, 2H), 7.29-7.42(m, 15H); LRMS ESI m/z 453 [M+H]+
Example 90 S-Methvl-5-(4-phenoxvpiperidln-1-yl]-2.2-dlphenvlh6xanamide
(Formula Removed)

Potassium hydroxide (512mg, 9.12mmol) was added to a solution of the product of example 86 (200mg, 0.46mmol) in 3-methyl-3-pentanol (4mL) and the mixture was heated under reflux for 20 hours. The reaction mixture was then cooled to room temperature, concentrated in vacuo and the residue was partitioned between ethyl acetate (20mL) and water (20mL). The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dlchloromethane:methanol:0.88 ammonia, 100:0 to 90:10:1, afforded the title compound as a colourless glass in 93% yield, 193mg.
. 1HNMR(400MHz, CDCI3) 5: 0.99(s, 6H), 1.25-1.29(m, 2H), 1.60-1.68(m, 2H), 1.89-1.93(m, 2H), 2.20-2.25(m, 2HJ, 2.42-2.46(m, 2H), 2.64-2.68(m, 2H), 4.20-4.27(m, 1H), 6.85-6.89(m, 3H), 7.20-7.26(m, 4H), 7.30-7.34(m, 4H), 7.37-7.40(m, 4H); LRMS ESI m/z 457 [M+H]+
Example 91 5-f4-r(3-Bromobenzvnoxvlpiperidln-1-vl)-S-methvl-2,2-d|phenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 87, using the same method as that described for example 90, as a colourless gum In 99% yield.
1HNMR(400MHz, CD3OD) 6: 0.97(s, 6H), 1.23-1.27(m, 2H), 1.48-1.57(m, 2H), 1.82-1.87(m, 2H), 2.07-2.12(m, 2H), 2.40-2.44(m, 2H), 2.62-2.66(m, 2H), 3.29-3.37(m, 1H), 4.48(s, 2H), 7.21-7.42(m, 13H), 7.49(s, 1H); LRMS ESI m/z 551 [M+H]+ •
Example 92 5-[4-(Benzvloxvtoiperldin-1-yl]-5-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
he title compound was prepared from the product of example 89, using the same method as that described for example 90, as a colourless glass in 79% yield.
1HNMR(400MHz, CD3OD) 5: 1.01(s, 6H), 1.28-1.30(m, 2H), 1.57-1.59(m, 2H), 1.86-1.89(m, 2H), 2.21(m, 2H), 2.40-2.45(m, 2H), 2.72(m, 2H), 3.38(m, 1H), 4.50(s, 2H), 7.23-7.39(m, 15H); LRMS APCI m/z 471 [M+H]+
Example 93 5-4-(2.4-Dlchloro-5-hvdroxv-phenoxv-plperidln-1-yl]-5-methvl-2.2-diphenvlhexanolc
acid
amide
(Formula Removed)
Diisopropyl azodicarboxylate (0.05mL, 0.26mmol) was added dropwise to a mixture of preparation 54 (50mg, 0.13mmol), 4,6-dichlorabenzene-1,3-dIol (47mg, 0.26mmol) and triphenylphosphine (69mg, 0.26mmol) in tetrahydrofuran (1mL) and the mixture left to stir for 7 days at room temperature. The solvent was concentrated in vacuo and the residue purified using an Isolute® SCX-2 cartridge, eluting with methanol followed by 1M ammonia in methanol. The appropriate fractions were combinedj evaporated under reduced pressure and the residue further purified by column chromatography on' silica gel, eluting with dichloromethanermethanol, 98:2 to 95:5, afforded the title compound as a colourless glass in 8% yield, 6mg.
1HNMR(400MHz, CD3OD) 5: 1.04(s, 6H), 1.28-1.32(m, 2H), 1.71-1.78(m, 2H), 1.86-1.92(m, 2H), 2.36-2.46(m, 4H), 2.69-2.75(m, 2H), 4.29 (m, 1H), 6.57(s, 1H), 7.21-7.39(m, 11H); LRMS ESI m/z 541 [M+H]+
Example 94
5-[4-(4-Cvano-2.5-dlfluoro-phenoxv)-plperidln-1 -yl]-S-methvl-2.2-diphenvlhexanoic acid amide
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 12mg, 0.29mmol) was added to a solution of the product of preparation 54 (100mg, 0.26mmol) In tetrahydrofuran (0.5mL) at room temperature and allowed to stir for 20 minutes before cooling to -70°C. The mixture was added into a solution of 2,4,5-trlfluorobenzonltrile (41 mg, 0.26mmol) in tetrahydrofuran (0.5ml) at -70°C and stirred for. 3 hours. The reaction was then allowed to warm to room temperature and stirred for a further 18 hours. The reaction was quenched with water (5 drops) and the solvent evaporated in vacuo. The residue was partitioned between ethyl acetate (40mL) and water (20mL), the organic layer was separated and washed with brine (20mL). The organic phase was dried over magnesium sulfate, concentrated in vacuo and the residue purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 90:10:1. The appropriate fractions were evaporated under reduced pressure to afford the title compound as a colourless glass in 40% yield, 54mg.
1HNMR(400MHz, CD3OD) 5: 0.99(s, 6H), 1.25-1.29(m, 2H), 1.66-1.75(m, 2H), 1.92-1.97(m, 2H) 2.25-2.30(m, 2H) 2.42-2.46(m, 2H), 4.43-4.49(m, 1H), 7.13-7.52(m, 12H); LRMS APCI m/z 518 [M+H]+
Example 95 5-[4-(3-hvdro)q/phepoxy>Diperidin-1-yl]-5-[riethyl-2.2-dlphenylhexanamlde
(Formula Removed)
Diisopropyl azodicarboxylate (0.23mL, 1.20mmol) was added dropwise to an ice cold solution of the product of preparation 54 (226mg, 0.594mmol), resorcinol (196mg, 1.71 mmol) and triphenylphosphine (312mg, 1.19mmol) in tetrahydrofuran (2mL) and the mixture stirred at room temperature for 12 hours. The solvent was removed under reduced pressure and the residue purified using an Isolate® SCX-2 cartridge, eluting with methanol, then with 1M ammonia in methanol. Basic fractions were concentrated in vacuo and further purified by chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 98:2:0.2 to 95:5:0.5. Appropriate fractions were concentrated In vacuo and half of the residue obtained (55mg) was further purified by preparative thin layer chromatography using a silica coated
plate and eluting with dlchloromethane:rnethanol:0.88ammonia 80:20:2 to afford the title compound as a gum In 14% yield.
1HNMR(400MHz, CD3OD) 5:1.05 (s, 6H), 1.30-1.34 (m, 2H), 1.66-1.74 (m, 2H), 1.91-1.96 (m, 2H), 2.34-2.47 (m, 4H), 2.70-2.79 (m, 2H), 4.21-4.27 (m, 1H), 6.32-6.38 (m, 3H), 7.00-7.05 (m, 1H), 7.23-7.40 (m, 10H); LRMS APCI m/z473 [M+H]+
Example 96 5-[4-(3-hvdroxv-2-methvlphenoxv^Dlperidln-1-yl]-5-methvl-2.2-dlphenvlhexanamlde
(Formula Removed)
Dilsopropyl azodlcarboxylate (0.1mL, 0.53mmol) was added dropwise to a solution of the product of preparation 54 (100mg, 0.263mmol), 2-methyl-resorclnol (130mg, 1.05 mmol) and trlphenylphosphine (139mg, 0.53mmol) In tetrahydrofuran (2mL) and the mixture stirred at room temperature for 12 hours. The solvent was removed under reduced pressure and purified using an Isolute® SCX-2 cartridge, eluting with methanol, then with 1M ammonia In methanol. Basic fractions were concentrated in vacuo and further purified by chromatography on silica gel, eluting with dich1oromethane:methanol:0.88ammonia, 98:2:0.2 to 95:5:0.5. Appropriate fractions were concentrated in vacuo and the residue further purified using a Phenomenex Curosil PFP column (21.2*150mm dimensions) on a preparative .Agilent 1100 HPLC. The two mobile phases were 0.1% v/v Formic acid (aq) (A) and 0.1% v/v Formic acid in acetonitrile (B), eluting with a gradient of 20-80% B over 18 minutes at a flow rate of 18ml/min. The peaks were detected using a UV detector at 225nm and appropriate fractions concentrated In vacuo.io afford the title compound as a gum In 9% yield. 1HNMR(400MHz, CD3OD) 5:1.06 (s, 6H), 1.28-1.34 (m, 2H), 1.71-1.81 (m, 2H), 1.89-1.94 (m, 2H), 2.02 (s, 3H), 2.37-2.46 (m, 4H), 2.68-2.77 (m, 2H), 4.24-4.31 (m, 1H), 6.37-6.41 (m, 2H), 6.86-6.90 (m, 1H), 7.23-7.40 (m, 10H); LRMS APCI m/z 487 [M+H]+
Example 97
5-{4-[(3'-hvdroxvbiPhenvl-3-vnmethoxvlpiperidin-1 -vl)-5-methvl-2.2-dlphenvlhexanenltrile
(Formula Removed)
1,-r-Bis (diphenylphosphino)ferrocenedichloro palladium(ll) (8mg, 0.09mmol) was added to a suspension of the product of example 87 (100mg, 0.19mmol), 3-hydroxyphenylboronic acid (52mg, 0.038mmol) and sodium carbonate (40mg, 0.038mmol) in tetrahydrofuran (5mL) and water (1mL) and the mixture was heated at 60°C for 12 hours. The suspension was allowed to cool to room temperature and then evaporated to dryness under reduced pressure, The residue was purified by chromatography on silica gel, elutlng with dichloromethane: methanol;O.B8 ammonia, 99:1:0 to 98:2:0.2, to give the title compound as a gum in 72% yield. 1HNMR(400MHz, CD3OD) 5: 1.09 (s, 6H), 1.52-1.56 (m, 2H), 1.61-1.68 (m, 2H), 1.93-1.96 (m, 2H), 2.24-2.42 (m, 2H), 2.51-2.55 (m, 2H), 2.81-2.84 (m, 2H), 3.45-3.49 (m, 1H), 4.58 (s, 2H), 6.75-6.78 (m, 1H), 7.02-7.07 (m, 2H), 7.21-7.43 (m, 13H), 7.47-7.50 (m, 1H), 7.54 (s, 1H); LRMS ESI m/z 545 [M+H]+
Example 98 5-{4-[(3'-hvdroxvbiphenvl-3-vfim6thoxvlpip6ridin-1-vl)-5-methvl-2.2-diphenvlhexanamlde
(Formula Removed)
A suspension of the product of example 97 (70mg, 0.13mmol) and powdered potassium hydroxide (144mg, 2.57mmol) in 3-methyl-4-pentanol (4mL) was heated under reflux for 36 hours. The reaction mixture was allowed to cool to room temperature and the solvent removed under reduced pressure. The residue was partitioned between ethyl acetate (30mL) and water (20mL). The organic layer was separated, dried over magnesium sulphate and concentrated in vacua. The residue was purified by chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 95:5:0.5 to 90:10:1. Appropriate fractions were concentrated in vacua and the residue further purified by chromatography on silica gel, elutlng with dichloromethane:methanol:0.88 ammonia, 98:2:0.2 to 95:5:0.5, to afford the title compound as a gum In 21% yield.
1HNMR(400MHz, CD3OD) 6: 1.05 (s, 6H), 1.22-1.35 (m, 2H), 1,62-1.68 (m, 2H), 1.85-1.93 (m, 2H), 2.35-2.45 (m. 4H), 2.78-2.82 (m, 2H), 3.43-3,49 (m, 1H), 4.57 (s, 2H), 6.75-6.78 (m, 1H), 7.02-7.07 (m, 2H), 7.21-7.40 (m, 13H), 7.47-7.50 (m, 1H), 7.54 (s, 1H); LRMS APCI m/z 563
Example 99 5-[3-((3-Methoxvphenoxvtezetidin-1-vl1-5-methvl-2.2-dlphenvlh6xanenltrile
(Formula Removed)
A mixture of the product of preparation 57 (500mg, 1.21mmol), caesium carbonate (1.18g, 3.64mmol) and 3-methoxyphenol (0.41 mL, 3.64mmol) in N.N-dimethylformamide (10mL) was stirred at 80°C for 18 hours. The reaction mixture was then concentrated in vacuo and the residue was partitioned between diethyl ether (50mL) and water (20mL). The aqueous layer was separated, extracted with diethyl ether (2x30mL) and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 90:10 to 75:25 then dichloromethane:methanol:0.88 ammonia, 100:0:0 to 95:5:0.5, to afford the title compound as a colourless gum in 71% yield, 380mg.
1HNMR(400MHz, CDCI3) 6: 0.90-1.03(m, 8H), 1.31-1.44(m, 2H), 2.41-2.56(m, 2H), 3.07-3.24(m, 2H), 3.42-3.54(m, 2H), 3.77(s, 3H), 4.63-4.74(m, 1H), 6.28-6.38(m, 2H), 6.48-6.55(m, 1H), 7.26-7.49(m, 11H); LRMS APCI m/z441 [M+H]+
Example 100 5-[3-(f3-Methoxyphenoxy)azetidln-1-yn-S-methvl-2,2-dlPhenvlhexanamide
(Formula Removed)

Potassium hydroxide (215mg, 3.83mmol) was added to a solution-of the product of example 99 (85mg, 0.19mmol) in 3-methyl-3-pentanol (5mL) and the mixture was heated under reflux for 24 hours. The reaction mixture was then cooled to room temperature, concentrated in vacuo and the residue was partitioned between ethyl acetate (20mL) and water (5mL). The aqueous layer was separated, extracted with ethyl acetate (20ml) and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 93:7:0.7, afforded the title compound as a colourless gum in 74% yield, 65mg.
'HNMR(400MHz, CDCI3) 6: 0.92(s, 6H), 1.12-1.23(m, 2H), 2.40-2.50(m, 2H>, 3.10-3.25(m, 2H), 3.44-3.58(m, 2H), 3.78(s, 3H), 4.62-4.72(m, 1H), 6.30-6.38(m, 2H), 6.47-6.54(m, 1H), 7.10-7.18(m, 1H), 7.22-7.45(m, 10H); LRWIS ESI m/z 459 [M+H]+
Example 101 6-r3-fBBnzvloxvtezetidln-1-yl]-5-methvl-2.2-dlPhenvlhexanenltrile
(Formula Removed)
Sodium hydride (60% dispersion in mineral oil, 24mg, 0.60mmol) was added to an Ice-cooled solution of the product of preparation 56 (166mg, O.SOmmol) In N.N-dimethylformamide (5mL) and the mixture was stirred for 30 minutes allowing the temperature to rise to 25°C. The reaction mixture was then re-cooled to 0°C, benzyl bromide (89uL, 0.75mmol) was added and the mixture was stirred at 0°C for 30 minutes. The reaction was quenched with 2M hydrochloric acid (2mL), basified to pH 8 with saturated sodium hydrogen carbonate solution and extracted with ethyl acetate (3x50mL). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 97:3:0.3, to afford the title compound as a colourless oil in 65% yield, 137mg. 1HNMR(400MHz, CDCI3) 6: 0.91(s, 6H), 0.90-0.97(m, 2H), 2.40-2.48(m, 2H), 2.97-3.06(m, 2H), 3.21-3.30(m, 2H), 4.07-4.17(m, 1H), 4.41(s, 2H), 7.26-7.46(m, 15H); LRMS APCI rn/z 425 [M+H]+
Example 102 S-[3-(Benzvloxy)azetldin-1-vl]-5-methvl-2.2-dlphenylhexanamlde
(Formula Removed)
The title compound was prepared from the product of example 101, using the same method as that described for example 100, as a colourless gum in 77% yield.
1HNMR(400MHz, CDCI3) 6: 0.89(s, 6H), 1.05-1.13(m,.2H), 2.32-2.41(m, 2H), 2.95-3.05(m, 2H), 3.15-3.25(m, 2H), 4.02-4.13(m, 1H), 4.39(s, 2H), 7.21-7.42(m, 15H); LRMS APCI m/z 443 [M+H]+
Example 103 5-Methvl-5-(3-phenoxvazetidln-1-yl]-2.2-diphenvlhexanenitrile

(Formula Removed)


The title compound was prepared from the product of preparation 65, using the same method as that described for preparation 62, as a colourless oil in 38% yield.
1HNMR(400MHz, CDCI3) 6: 0.95 (s, 6H), 1.34-1.41 (m, 2H), 2.43-2.54 (m, 2H), 3.15-3.22 (m, 2H), 3.45-3.55 (m, 2H), 4.65-4.75 (m, 1H), 6.73-6.78 (m, 2H), 6.90-6.98 (m, 1H), 7.22-7.45 (m, 12H); LRMS APCI m/z411 [M+H]+
Example 104 5-Methvl-5-(3-phenoxvazetidln-i-yl)-2.2-diphenvlhexanamlde

(Formula Removed)

The title compound was prepared from the product of example 103, using the same method as that described for example 100, as a white solid in 88% yield.
1HNMR(400MHz, CDCI3) 6: 0.91(s, 6H), 1.12-1.20(m, 2H), 2.42-2.48(m, 2H), 3.12-3.18(m, 2H), 3.45-3.55 (m, 2H), 4.62-4.73(m, 1H), 5.55(brs, 2H), 6.75-6.78(m, 2H), 6.92-6.96(m, 1H), 7.20-7.41 (m, 12H); LRMS APCI m/z 429 [MI+H]+
Example 105 S-f3-(4-Methoxvphenoxvtezetidin-1-yl]-5-methvl-2,2-dlphenvlhexanenitrile
(Formula Removed)
The title compound was prepared from the product of preparation 57 and 4-methoxy phenol, using the same method as that described for example 99, as a colourless gum in 55% yield. 1HNMR(400MHz, CDCI3) 5: 0.98(s, 6H), 1.33-1.45(m, 2H), 2.45-2.55(m, 2H), 3.14-3.24(m, 2H), 3.42-3.55(m, 2H), 3.78(s, 3H), 4.5a-4.68(m, 1H), 6.66-6.74(m, 2H), 6.76-6.85(m, 2H), 7.25-7.47(m, 1 0H); LRMS APCI m/z 441 [M+H]+
Example 106 S-3-fc-Methoxvhenoxv)azetldln-1-yl]-S-methvl-2.2-dlphenvlhexanarnlde
(Formula Removed)
Potassium hydroxide (135mg, 2.41mmol) was added to a solution of the product of example 105 (53mg, 0.12mmol) in 3-methyl-3-pentanol (5mL) and the mixture was heated under reflux for 18 hours. The reaction mixture was then cooled to room temperature, concentrated in vacuo and the residue was partitioned between ethyl acetate (20mL) and water (5mL). The aqueous layer was separated, extracted with ethyl acetate (2x20mL) and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo to give a colourless oil in 96% yield, 53mg.
1HNMR(400MHz, CDCI3) 5: 0.92(3, 6H), 1.12-1.23(m, 2H), 2.40-2.50(m, 2H), 3.10-3.25(m, 2H), 3.44-3.58(m, 2H), 3.78(s, 3H), 4.62-4.72(m, 1H), 6.30-6.38(m, 2H), 6.47-6.54(m, 1H), 7.10-7.18(m, 1H), 7.22-7.45(m, 10H); LRMS ESI mlz 459 [M+H]+
Example 107 5-[3-(4-hvdroxvphenoxvtezetidin-1-yl]-5-methvl-2.2-diDhBnvlhexanamlde

(Formula Removed)
The product of example 106 (53mg, 0.16mmol) was dissolved In dichloromethane (5mL) and the solution was cooled to 0°C. Boron tribromide (1M in dichloromethane, 0.52mL, 0.52mmol) was added and the solution was stirred at 0°C for 35 minutes. Further boron tribromide (1M in dichloromethane, 0.52mL, 0.52mmol) was added and stirring continued at 0°C for 30 minutes. The reaction was then quenched with saturated sodium hydrogen carbonate solution (20mL)
and stirred at room temperature for 18 hours. The aqueous layer was separated, extracted with ethyl acetate (25mL) and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo to give a gum. The gum was re-dissolved in dichloromethane (5mL) and the solution was cooled to -10°C. Boron tribromide (1M In dlchloromethane, 0.52mL, 0.52mmol) was added and the mixture was stirred at -10°C for 1 hour. The reaction was then quenched with saturated sodium hydrogen carbonate solution (20mL) and the organic layer was separated and extracted with ethyl acetate (20mL). The combined organic solution was dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate/methanol/0.88 ammonia (90/10/1), 75:25 to 50:50, to afford the title compound as a colourless foam in 27% yield (14mg).
1HNMR(400MHz, CDCI3) 5: 0.92(s, 6H), 1.13-1.26(m, 2H), 2.40-2.50(m, 2H), 3.08-3.24{m, 2H), 3.42-3.58(m, 2H), 4.52-4.63(m, 1H), 5.50-5.68 (brs, 2H), 6.53-6.62(m, 2H), 6.67-6.78(m, 2H), 7.21-7.42(m, 10H); LRMS APCI m/z 445 [M+H]+
Example 108 5-[3-(3-Hvdroxvphenoxv)azetidin-1-yl]-5-methvl-2.2-diphenvlhexanamidB
(Formula Removed)
Boron tribromide (1M in dichloromethane, 1.75mL, 1.75mmol) was added to an ice-cooled solution of the product of example 100 (200mg, 0.44mmol) in dichloromethane (5mL) and the mixture was stirred at 0°C for 1 hour. Further boron tribromide (1M in dichloromethane, 0.5ml, 0.5mmol) was added and the mixture was stirred at 0°C for 30 minutes. The reaction was then quenched with 1M sodium hydroxide solution (5mL), diluted with dichloromethane (20mL) and stirred at room temperature for 40 minutes. The aqueous layer was separated, extracted with ethyl acetate (2x25mL) and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethyl acetate/methanol/0.88 ammonia (90/10/1), 75:25 to 50:50,'afforded the title compound as a colourless foam In 91% yield, 176mg.
1HNMR(400MHz, CDCI3) 5: 1.10(8, 6H), 1.22-1.34(m, 2H), 2.42-2.55(m, 2H), 3.28-3.40(m, 2H), 3.65-3.88(m, 2H), 4.70-4.80(m, 1H), 5.55-5.70(brs, 2H), 6.23-6.36(m, 2H), 6.45-6.53(m, 1H), 7.03-7.12(m, 1H), 7.19-7.39(m, 10H); LRMS ESI m/z 445 [M+H]+
Example 109 5-[3-(2-Hvdroxvphenoxv)azetidln.1-yl]-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
Ammonium formate (25mg, 0.4mmol) was added to a mixture of the product of preparation 63 (35mg, 65umol) and 20% Pd(OH)2/C (10mg) In ethanol (10mL) and the mixture was heated under reflux for 2 hours. The reaction mixture was cooled to room temperature, further ammonium formate (25mg, 0.4mmol) and 20% Pd(OH)z/C (10mg) were added and the mixture was re-heated under reflux for 2 hours. The reaction mixture was filtered through Arbocel* washing through with methanol, and the filtrate was concentrated in vacuo. The residue was diluted with saturated sodium hydrogen carbonate solution extracted with ethyl acetate (2x20mL) and the combined organic solution was dried over magnesium sulfate and concentrated In vacuo. Purification of the residue by column chromatography on silica gel, eluting with ethyl acetate:methatiol, 95:5, then afforded the title compound as a colourless oil in quantitative yield, 3Gmg.
1HNMR(400MHz, CDCI3) 6: 1.02(s, 6H), 1.22-1.32(m, 2H), 2.31-2.49(m, 2H), 2.57-2.72(m, 2H)r 3.98-4.04(m, 1H), 4.15-4.24(m, 2H), 5.40-5.70(brm, 2H), 6.77-6.86(m, 4H), 7.22-7.38(m, 10H); LRMS APCI mlz 445 [M+H]+
Example 110 5-(3-(2.4-Plchloro-5-hvdrQXV-phenoxy)-az6tidtn-1-v»-5-methvl-2.2-diDhanvlhexanamlde

(Formula Removed)

Potassium hydroxide (523mg, 9.33mmol) was added to a solution of the product of preparation 68 (250mg, 0.46mmol) in 3-methy!-3-pentanol (5mL) and the mixture was heated under reflux for 18 hours. The reaction mixture was then cooled to room temperature, concentrated in vacuo and the residue was partitioned between ethyl acetate (20mL) and water (20mL). The aqueous layer was separated and 'extracted with ethyl acetate (20mL) and the combined organic solution was dried over magnesium sulphate and concentrated In vacuo. The crude material was treated with 4M hydrochloric acid in dioxane (10mL, 40mmol)
and the solution stirred at 60°C for 30 minutes. The dioxane was removed in vacuo and the residue basified with 0.88 ammonia. The aqueous layer was extracted with ethyl acetate (2x20mL). The combined organic solution was dried over magnesium sulphate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol 100:1 to 10:1 to afford the title compound as a colourless oil in 61% yield, 147mg.
1HNMR(400MHz, CDCI3) 6: 0.98 (s, 6H), 1.18-1.25 (m, 2H), 2.41-2.55 (m, 2H), 3.32-3.38 (m, 2H), 3.75-3.82 (m, 2H), 4.68-4.75 (m, 1H), 5.65-5.75 (m, 1H), 5.95-6.05 (m, 1H), 6.43 (s, 1H), 7-20-7.40 (m, 11H); LRMS APCI m/z 513 [M+H]+
Example 111 5-(3-(4.5-Dichloro.2-hvdroxv-phenoxy)-azetidln-1-yl)-5-methyl-2.2-diphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of preparation 70, using the same method as described for example 110, as a colourless oil In 53% yield.
1HNMR(400MHz, CDCI3) 6:1.02 (s, 6H), 1.22-1.30 (m, 2H), 2.35-2.50 (m, 2H), 2.60-2.75 (m, 2H), 3.95-4.01 (m, 1H), 4.10-4.25 (m, 2H), 5.40-5.60 (m, 2H), 6.92-6.98 (m, 2H), 7-20-7.40 (m, 10H); LRMS ESI m/z 513
Example 11.2 5-[3-((4-Chloro-3-methoxv-phenoxy)-azetidln-1-vl1-S-methvl-2.2-dlphenvl-hexanenitrlle
(Formula Removed)
The title compound was prepared from 4-chloro-3-methoxyphenol (EP230379, p52) and the product of preparation 57, using the same method as that described for example 99, as a colourless oil in 85% yield.
1HNMR(400MHz, CDCI3) 5; 0.95 (s, 6H), 1 .35-1.40 (m, 2H), 2.45-2.53 (m, 2H), 3.16-3.20 (m, 2H), 3.45-3.52 (m, 2H), 3.86 (s, 3H), 4.62-4.70 (m, 1H), 6.20-6.25 (m, 1H), 6.40-6.43 (m, 1H), 7-18-7.45 (m, 1 1H); LRMS APCI mtz 475
Example 113 5-(3-(4-ChlorQ-3-methoxv-phenoxv^-azetidln-1-yl)-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 112, using the same method as that described for example 100, as a colourless oil in 91% yield.
1HNMR(400MHz, CDCI3) 5: 0.85 (s, 6H), 1.08-1.22 (m, 2H), 2.38-2.50 (m, 2H), 3.15-3.20 (m, 2H), 3.40-3.55 (m, 2H), 3.85 (s, 3H), 4.60-4.72 (m, 1H), 5.30-5.55 (m, 2H), 6.20-6.23 (m, 1H), 6.38-6.41 (m, 1H). 7-18-7.40 (m, 11H); LRMS APCI m/z 493 [M+H]+
Example 114 5-(3-(4-Chloro-3-hvdroxv-phenoxv)-azetidln-1-vl}-5-methvl-2.2-dlphenvihexanamlde
(Formula Removed)
Boron tribromide (1M in dichloromethane, 1.75mL, 1.75mmol) was added to an ice-cooled solution of the product of example 113 (180mg, 0.36mmol) in dichloromethane (5mL) and the mixture was stirred at 0°C for 1.5 hour. The reaction was then quenched with 0.88 ammonia (30mL) and the solution stirred at room temperature for 18 hours. The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane to dichloromethane/methanol/0.88 ammonia (97:3:0.3), afforded the title compound as a colourless foam in 93% yield, 270mg
1HNMR(400MHz, CDCI3) 5: 0.85 (s, 6H), 1.08-1.22 (m, 2H), 2.40-2.50 (m, 2H), 3.10-3.20 (m, 2H), 3.50-3.58 (m, 2H), 4.58-4.66 (m, 1H), 5.45-5.55 (m, 1H), 5.75-5.90 (m, 1H), 6.25-6.32 (m, 1H), 6.38-6.40 (m, 1H). 7-15-7.40 (m, 11H); LRMS APCI m/z 479 [M+H]+
Example 115
5-[3-(3-Hvdroxv-benzvloxy)-azetldin-1 -yl]-5-methvl-2.2-diphenvl-hexanoic acid amide
(Formula Removed)
The product of preparation 73 (65mg, 0.131mmol) was treated with 4M hydrochloric acid In dioxane (2mL, 8mmol), water (0.2 ml) was added and the solution stirred at 85°C for 30 minutes. The dioxane was removed in vacuo and the residue partitioned between ethyl acetate (25ml) and saturated sodium hydrogen carbonate solution (20mL). The aqueous layer was extracted with ethyl acetate (20mL). The combined organic solution was dried over 'magnesium sulphate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate:methanol:0.88 ammonia (90/10/1), 75:25 to 50:50, to afford the title compound as a colourless foam in 70% yield, 42mg.
1HNMR(400MHz, CDCI3) B: 0.90(s, 6H), !16-1.25(m, 2H), 2.38-2.48(m, 2H), 3.02-3.12 (m, 2H), 3.28-3.40(m, 2H), 4.06-4.17(m, 1H), 4.31 (s, 2H), 5.58-5.74 (br s, 2H), 6.72-6.83 (m, 3H), 7,12-7.20(m, 1H), 7.21-7.40 (m, 10H); LRMS APCI m/z 459 [M+H]+
Example 116 5-[3-((2-Chloro-5-methoxv-phenoxv)-azetldln-1-vl1-5-methvl-2,2-diphenvl-hexanenitrile
(Formula Removed)
The title compound was prepared from the product of preparation 57 and 2-chloro-5-methoxyphenol, using the same method as that described for example 99, as a brown gum In 55% yield.
1HNMR(400MHz, CDCI3) 5: 0.96 (s, 6H), 1.31-1.44(m, 2H), 2.40-2.57 (m, 2H), 3.14-3.35 (m, 2H), 3.40-3.60 (m, 2H), 3.77(s, 3H), 4.64-4.79 (m, 1H), 6.20-6.25 (m, 1H), 6.39-6.47(m, 1H), 7.20-7.48(m, 11H); LRMS APCI m/z 475 [M+H]+
Example 117 5-[3-(2-Chloro-5-methoxv-phenoxy)-azetldin-1-yl]-5-methvl-2.2-diphenvl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product of example 116, using the same method as that described for example 100, as a colourless gum in 61% yield.
1HNMR(400MHz, CDCI3) 5: 0.92 (s, 6H), 1.11-1.20 (m, 2H), 2.40-2.48 (m, 2H), 3.15-3.24 (m, 2H), 3.42-3.55 (m, 2H), 3.76 (s, 3H), 4.64-4.72 (m, 1H), 5.48-5.75 (m, 2H), 6.20-6.25 (m, 1H), 6.38-6.45 (m, 1H). 7.20-7.41 (m, 11H); LRMS APCI m/z 493 [M+H]+
Example 118 5-[3-((2-Chloro-5-hvdroxv-phenoxy)-azetldln-1-yl]-5-methvl-2,2-diphenvl-hexanoic acid amide
(Formula Removed)
Boron tribromlde (1M in dichloromethane, 1.42mL, 1.42mmol) was added to an ice-cooled solution of the product of example 117 (70mg, 0.142mmol) in dichloromethane (5mL) and the mixture was stirred at 0°C for 1 hour. The reaction was then quenched with 0.88 ammonia (20ml) and the solution stirred at room temperature for 18 hours. The organic layer was separated. The aqueous layer was extracted with dichloromethane (20mls). The combined organic solution was washed with saturated sodium hydrogen carbonate solution (10mL) and dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethyl acetate:methanol:0.88 ammonia (90/10/1), 85:15 to 50:50. The resulting gum was dissolved in methanol (5mls) and 1N hydrochloric acid in diethyl ether (0.5ml) added. The solution was evaporated and the solid recrystallised from ethyl acetate / methanol to give the title compound hydrochlorlde salt as a purple solid in 30% yield, 22mgs.
1HNMR(400MHz, CD3OD) 5: 1.28 (s, 6H), 1.33-1.44 (m, 2H), 2.40-2.48 (m, 2H), 4.02-4.30 (m, 2H), 4.33-4.62 (m, 2H), 4.95-5.06 (m, 1H), 6.20-6.28 (m, 1H)-, 6.44-6.49 (m, 1H), 7-15-7.20 (m, 1H), 7.24-7.41 (m, 10H); LRMS APCI m/z 479 [M+H]+
Example 119 5-[3-((3-Fluoro-S-methoxv-phenoxy)-azetidin-1-yl]-5-methvl-2.2-dlphenvl-hexanenltrile
(Formula Removed)
The title compound was prepared from 3-fluoro-5-methoxyphenol (W02005037763, p95) and the product of preparation 57, using the same method as that described for example 99, as a colourless oil In 90% yield.
1HNMR(400MHz, CDCI3) 6: 0.95 (s, 6H), 1.35-1.40 (m, 2H), 2.45-2.53 (m, 2H), 3.06-3.15 (m, 2H), 3.40-3.48 (m, 2H), 3.75 (s, 3H), 4.58-4.64 (m, 1H), 6.05-6.12 (m, 2H), 6.20-6.26 (m, 1H), 7-22-7.45 (m, 10H); LRMS APCI m/z 459 [M+H]+
Example 120 5-[3-((3-Fluoro-5-methoxv-phenoxy)-azetldin-1-yl]-5-methvl-2,2-diphenvlhexanamide

(Formula Removed)
The title compound was prepared from the product of example 119, using the same method as that described for example 100, as a colourless oil in 90% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.42-1.55 (m, 2H), 2.40-2.48 (m, 2H), 3.06-3.15 (m, 2H), 3.40-3.45 (m, 2H), 3.78 (s, 3H), 4.58-4.66 (m, 1H), 5.40-5.55 (m, 2H), 6.03-6.12 (m, 2H), 6.20-6.25 (m, 1H), 7.22-7.45 (m, 10H).
Example 121 5-[3-(3-Fluoro-5-hvdroxv-phenoxv)-azetidin-1-yl)-5-methvl-2.2-diphenvlhexanamide

(Formula Removed)
The title compound was prepared from the product of example 120, using the same method as that described for example 108, as a colourless oil in 25% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.20-1.26 (m, 2H), 2.40-2.46 (m, 2H), 3.20-3.28 (m, 2H), 3.60-3.65 (m, 2H), 4.64-4.70 (m, 1H), 5.50-5,60 (m, 1H), 6.00 (s, 1H), 6.02-6.06 (m, 1H), 6.18-6.23 (m, 1H), 6.25-6.35 (m, 1H), 7.20-7.35 (m, 10H); LRMS APCI m/z 463 [M+H]+
Example 122 5-[3-(3-Chloro-5-methoxv-phenoxy)-a26tldin-1-yl]-5-methvl-2.2-dlPhenvl-hexanenltrlle
(Formula Removed)
The title compound was prepared from 3-chloro-5-methoxyphenol and the product of preparation 57, using the same method as that described for example 99, as a colourless oil in 75% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.35-1.40 (m, 2H), 2.45-2.53 (m, 2H), 3.06-3.15 (m, 2H), 3.40-3.48 (m, 2H), 3.78 (s, 3H), 4.58-4.66 (m, 1H), 6,20 (s, 2H), 6.35 (s, 1H), 6.50 (s, 1H), 7-22-7.45 (m, 10H); LRMS APCI m/z 475 [M+H]+
Example 123 5-[3-(3-Chloro-5-methoxv-phenoxy)-azetidin-1-yl]-5-methvl-2.2-diphenvlhexanamide

(Formula Removed)
The title compound was prepared from the product of example 122, using the same method as that described for example 100, as a colourless oil In 90% yield.
1HNMR(400MHz, CDCI3) 8: 0.95 (s, 6H), 1.15-1.20 (m, 2H), 2.38-2.45 (m, 2H), 3.02-3.10 (m, 2H), 3.37-3.43 (m, 2H), 3.75 (s, 3H), 4.55-4.63 (m, 1H), 5.40-5.65 (m, 2H), 6.18 (s, 1H), 6.30 (s, 1H), 6.48 (s, 1H), 7.20-7.40 (m, 10H); LRMS APCI m/z 493 [M+H]+
Example 124 5-(3-(3-Chloro-S-hvdroxv-phenoxv)-azetidin-1-yl)-5-methvl-2.2-diphenvlhexanamide
(Formula Removed)
The title compound was. prepared from the product of example 123, using the same method as that described for example 114, as a colourless oil in 92% yield.
1HNMR(400MHz, CDCI3) 5: 0.90 (s, 6H), 1.08-1.18 (m, 2H), 2.35-2.45 (m, 2H), 3.06-3.15 (m, 2H), 3.40-3.46 (m, 2H), 4.55-4.60 (m, 1H), 5.45 (brs, 2H), 6.15 (s, 1H),;6.25 (s, 1H), 6.40 (s, 1H), 7.20-7.40 (m,10H)
Example 125 5-[3-(f4-Fluoro-2-methoxv-phenoxy)-azetidin-1-yl]-S-methvl-2.2-diphenvl-hexanenitrlle
(Formula Removed)
The title compound was prepared from 4-fluoro-2-methoxyphertol and the product of preparation 57, using the same method as that described for example 99, as a colourless oil in 72% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.35-1.40 (m, 2H), 2.45-2.53 (m, 2H), 3.20-3.25 (m, 2H), 3.42-3.48 (m, 2H), 3.83 (s, 3H), 4.58-4.66 (m, 1H), 6.53-6.65 (m, 3H), 7-22-7.45 (m, 10H); LRMS APCI m/z459 [M+H]+
Example 126 5-[3-((4-Fluoro-2-methoxv-phenoxy)-azetidln-1-yl]-5-methvl-2.2-dlphenvlhexanamide
(Formula Removed)
The title compound was prepared from the product of example 125, using the same method as that described for example 100, as a colourless oil in 87% yield.
1HNMR(400MHz, CDCI3) Q: 0.95 (s, 6H), 1.10-1.18 (m, 2H), 2.40-2.48 (m, 2H), 3.15-3.20 (m, 2H), 3.40-3.46 (m, 2H), 3.80 (s, 3H), 4.58-4.66 (m, 1H), 5.50-5.75 (m, 2H), 6.48-6.65 (m, 3H), 7-22-7.40 (m, 10H); LRMS APCI m/z 477 [M+H]+
Example 127 5-[3-(4-Fluoro-2-hvdroxv-phenoxy)-azetidln-1-vll-5-methvl-2.2-dlPhenvlhexanamlde

(Formula Removed)
The title compound was prepared from the product of example 126, using the same method
as that described for example 114, as a colourless oil in 32% yield.
1HNMR(400MHz, CDCI3) 6: 0.98 (s, 6H), 1.20-1.28 (m, 2H), 2.35-2.48 (m, 2H), 2.56-2.68 (m,
2H), 3.95-3.42 (m, 1H), 4.05-4.18 (m, 1H), 4.18-4.25 (m, 1H), 5.40-5.65 (m, 2H), 6.45-6.53
(m, 1H), 6.55-6.60 (m, 1H), 6.72-6.78 (m, 1H), 7.20-7.35 (m, 10H); LRMS APCI m/z 463
[M+H]+
Example 128
5-[3-(2.6-Plchloro-3-hvdroxv-benzvloxv)-azetidin-1-v
amide
5-methvl-2.2-diphem/l-hexanolc acid
(Formula Removed)
The product of preparation 78 (150mg, 0.265mmol) was treated with 4M hydrochloric acid in dioxane (5mL, 20mmol) and water (0.5 ml) and the solution stirred at 70°C for 25 minutes. The dioxane was removed in vacuo and the residue partitioned between ethyl acetate (30ml) 5 and saturated sodium hydrogen carbonate solution (20mL). The aqueous layer was extracted with ethyl acetate (20mL). The combined organic solution was dried over magnesium sulphate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with pentaneiethyl acetate/methanol/0.83 ammonia (90/10/1), 5:1 to 1:3, to afford the title compound in 52% yield, 73mg.
10 1HNMR(400MHz, CDCI3) 5: 1.22 (s, 6H), 1.44-1.53 (m, 2H), 2.60-2.68 (m, 2H), 3.60-3.68 (m, 2H), 4.26-4.37 (m, 2H), 4.57-4.64 (m, 1H), 4.70 (s, 2H), 5.48-5.55 (br m, 1H), 5.78-5.84 (br m, 1H), 7.06-7.12 (m, 1H), 7.18-7.23 (m, 1H), 7.23-7.38 (m, 10H); LRMS APCI m/z 527[M+H]+
Example 129 15 4-f1-f3-(3-Methoxv-Phenoxy)-azetldin-1-yl]-cvclopentylV2.2-diphenyl-butyronitrile
(Formula Removed)
The title compound was prepared from the product of preparation 84 and 3-methoxyphenol, using a similar method to that described in example 99, in 73% yield. 1HNMR(400MHz, CDCI3) 5: 1.25-1.38 (m, 2H), 1.40-1.65 (m, 6H), 1.66-1.76 (m, 2H), 2.46-20 2.57 (m, 2H), 3.06-3.16 (m, 2H), 3.48-3.57 (m, 2H), 3.78.(s, 3H), 4.64-4.72 (m, 1H), 6.34 (s, 1H), 6.33-6.37 (m, 1H), 6.48-6.53 (m, 1H), 7.13-7.19 (m, 1H), 7.27-7.46 (m, 10H); LRMS APCI m/z 467 [M+H]+
Example 130 25 4-(1-f3-(3-Methoxv-phenoxy)-azetldin-1-yl]-cvcJopentvll-2.2-dlphenvl-butvramlde
(Formula Removed)
The title compound was prepared from the product of example 129 using a similar method to
that described for example 106, in 48% yield.
1HNMR(400MHz, CDCl3) 5: 1.22-1.70 (m, 10H), 2.46-2.53 (m, 2H), 3.07-3.15 (m, 2H), 3.47-
3.59 (m, 2H), 3.77 (s, 3H), 4.63-4.73 (m, 1H), 5.44-5.60 (br m, 2H), 6.33 (s, 1H), 6.33-6.36
(m, 1H), 6.48-6.53 (m, 1H), 7.11-7.18 (m, 1H), 7.20-7.40 (m, 10H); LRMS APCI m/z
485[M+H]+
Example 131 (
4-f1-f3-(3-Hydroxv-phenoxy)-azetldin-1-yl]-cvclopentvlV-2.2-diphenvl-butvramlde
(Formula Removed)
The title compound was prepared from the product of example 130 using a similar method to that described for example 108, in 53% yield.
1HNMR(400MHz, CDCI3) 8: 1.31-1.47 (m, 6H), 1.48-1.60 (m, 2H), 1.63-1.77 (m, 2H), 2.45-2.54 (m, 2H), 3.22-3.28 (m, 2H), 3.73-3.80 (m, 2H), 4.75-4.83 (m, 1H), 5.40-5.55 (br m, 1H), 6.24 (s, 1H), 6.36-6.39 (m, 1H), 6.48-6.55 (m, 1H), 6.56-6.67 (br m, 1H), 7.08-7.7.16 (m, 1H), 7.17-7.38 (m, 10H); LRMS APCI m/z 471[M+H]+
Example 132 5-[3-(2-Fluoro-3-roethoxv^phenoxv)-az@tldin-1-yl]-5-methvl-2.2-diphenvl-hexanenitrile
(Formula Removed)
The title compound was prepared from the product of preparation 57 and 2-fluoro-3-methoxyphenol (J. Comb. Chem. 2002, 4, 329), using a similar method to that described for example 99, In 73% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.34-1.40 (m, 2H), 2.44-2.53 (m, 2H), 3.20-3.27 (m, 2H), 3.43-3.52 (m, 2H), 3.88 (s, 3H), 4.65-4.74 (m, 1H), 6.34-6.39 (m, 1H), 6.58-6.64 (m, 1H), 6.88-6.95 (m, 1H), 7.25-7.47 (m, 10H); LRMS APCI m/z 459 [M+H]+
Example 133 • •
S-ra-te-Fluoro-a-methoxv-phenoxy)-azetldin-l -yl]-5-methvl-2.2-dlPhenvl-hexanoic acid amide

(Formula Removed)
The title compound was prepared from the product of example 132, using the same method as'that described for example 100, as a colourless oil in 72% yield.
1HNWIR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.17-1.25 (m, 2H), 2.40-2.48 (m, 2H), 3.20-3.28 (m, 2H), 3.50-3.60 (m, 2H),.4.65-4.74 (m, 1H), 5.46-5.75 (br m, 2H), 6.20-6.27 (m, 1H), 6.56-6.63 (m, 1H), 6.80-6.86 (m, 1H), 7.25-7.40 (m, 10H); LRMS APCI m/z 477 [M+H]+
Example 134
5-[3-((2-Fluoro-3-hvdroxy-phenoxy)-azetidin-1-vl]-5-metnyl-2.2-diphenyl-hexanoic acid amide
(Formula Removed)
Boron'tribromide (1M in dichloromethane, 1.5mL, 1.5mmol) was added to an ice-cooted solution of the product of example 133 (45mg, 0.094mmol) in dichloromethane (5mL) and the mixture was stirred at 0°C for 45 minutes. The reaction was warmed to room temperature. After 15 mln, a further 1.5mL boron tribromide was added. After 20 minutes, the reaction was quenched with 0.88 ammonia (20mL) and the solution stirred at room temperature for 18 hours. The organic layer was separated and washed with saturated sodium hydrogen carbonate solution (10mL) and dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with
dichioromethane:methanol:0.88 ammonia 100:0:0 to 98:2:0.2 to give the title compound in 100% yield (44mg).
1HNMR(400MHz, CDC13) 6: 0.95 (s, 6H), 1.17-1.26 (m, 2H), 2.43-2.49 (m, 2H), 3.20-3.28 (m, 2H), 3.45-3.60 (m, 2H), 4.65-4.74 (m, 1H), 5.49-5.76 (br m, 2H), 6.20-6.27 (m, 1H), 6.57-6.62 (m, 1H), 6.80-6.85 (m, 1H), 7.23-7.38 (m, 10H); LRMS APCI m/z 463 [M+H]+
Example 135 5-[3-(2-Fluoro-5-methoxv-phenoxy)-azetldin-1-vl1-S-methvl-2.2-diphenvl-hexanenltrlle
(Formula Removed)
The title compound was prepared from the product of preparation 57 and 2-fluoro-5-methoxyphenol (J. Can. Chem. 1988, 66,1479), using a similar method to that described for example 99, in 68% yield.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.36-1.42 (m, 2H), 2.44-2.53 (m, 2H), 3.20-3.27 (m, 2H), 3.43-3.52 (m, 2H), 3.77 (s, 3H), 4.65-4.74 (m, 1H), 6.27-6.34 (m, 1H), 6.38-6.42 (m, 1H), 6.95-7.02 (m, 1H), 7.25-7.47 (m, 10H); LRMS APCI m/z 459 [M+H]+
Example 136 5-[3-(2-Fluoro-5-methoxv-phenoxvV-azetidin-1-yl]-S-methvl-2.2-dlphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 135, using the same method as that described for example 100, as a colourless oil in 96% yield.
1HNMR(400MHz, CDCI3) 5: 0.92 (s, 6H), 1.12-1.20 (m, 2H), 2.40-2.48 (m, 2H), 3.16-3.21 (m, 2H), 3.43-3.50 (m, 2H), 3.76 (s, 3H), 4.60-4.72 (m, 1H), 5.46-5.60 (br m, 1H), 5.65-5.75 (br m, 1H), 6.25-6.33 (m, 1H), 6.34-6.40 (m, 1H), 6.91-6.99 (m, 1H), 7.22-7.40 (m, 10H); LRMS APCI m/z 477 [M+H]+
Example 137 5-[3-((2-Fluoro-5-hvdroxv-phenoxy)-azeMn-1-vl1-5-methvl-2.2-diphenvl-hexanoic acid amide

(Formula Removed)
The title compound was prepared from the product of example 136 using the same method as that described for example 118, as a colourless oil in 51 % yield.
1HNMR(400MHz, CDCI3) 5: 1.04 (s, 6H), 1.22-1.33 (m, 2H), 2.46-2.57 (m, 2H), 3.43-3.55 (m, 2H), 3.92-4.00 (m, 2H), 4.75-4.86 (m, 1H), 5.72-5.82 (br m, 1H), 6.35-6.48 (m, 3H), 6.83-6.92 (m, 1H), 7.20-7.38 (m, 10H); LRMS APCI m/z463 [M+H]+*
Example 138 5-[3-(4-ChlQro-3-hvdroxv-benzvloxv)-azetidln-1-yl]-5-methvl-2.2-diphenvl-hexanoic acid amide



(Formula Removed)
The title compound was prepared from the product of preparation 86, using the same method as that described for example 115, as a colourless oil In 37% yield.
1HNMR(400MHz, CDCI3) 6: 0.88 (s, 6H), 1.15-1.20 (m, 2H), 2.38-2.45 (m, 2H), 3.00-3.08 (m, 2H), 3.26-3.36 (m, 2H), 4.03-4.15 (m, 1H), 4.27 (s, 2H), 5.55-5.80 (br m, 2H), 6.73-6.78 (m, 1H), 6.95 (s, 1 H), 7.20-7.38 (m, 11H); LRMS APCI m/z 493 [M+H]+
Example 139 4-{1-[3-(4-Chloro-3-hvdroxv-phenoxv)-azetidln-1-vl1-cvcloDentvll-2.2-dlphenvl-butvramlde
(Formula Removed)
The title compound was prepared from the product of preparation 88, using the same method as that described for example 115, as a colourless oil in 20% yield.

1HNMR(400MHz, CDCI3) 6: 1.22-1.60 (m, 8H), 1.60-1.73 (m, 2H), 2.43-2.55 (m, 2H), 3.14-3.20 (m, 2H), 3.60-3.68 (m, 2H), 4.62-4.73 (m, 1H), 5.48-5.62 (br m, 1H), 6.11-6,25 (br m, 1H), 6.26-6.35 (m, 1H), 6.36-6.40 (m, 1H), 7.15-7.38 (m, 11H); LRWIS APCI m/z 505 [M+H]+
1
Example 140 5-[3-((3-Bromo-5-methoxv-Phenoxy)-azetidin-1-vl1-5-m6thvl-2.2-dlPhenvl-hexanenitrlle
(Formula Removed)
The title compound was prepared from the product of preparation 57 and the product of preparation 89, using a similar method to that described for example 99, in 90% yield. 1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.33-1.40 (m, 2H), 2.42-2.53 (m, 2H), 3.06-3.18 (m, 2H), 3.38-3.50 (m, 2H), 3.75 (S, 3H), 4.60-4.66 (m, 1H), 6.25 (s, 1H), 6.48 (s, 1H), 6.67 (s, 1H), 7.24-7.46 (m, 10H); LRMS ESI m/z 519 [M+H]+
Example 141
5-[3-((3-Bromo-5-methoxv-phenoxv)-azetldln-1 -vl1-5-methvl-2.2-diphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of example 140, using the same method as that described for example 100, as a colourless oil in 80% yield.
1HNMR(400MHz, CDCI3) δ: 0.92 (s, 6H), 1.12-1.18 (m, 2H), 2.38-2.46 (m, 2H), 3.05-3.13 (m, 2H), 3.37-3.44 (m, 2H), 3.75 (s, 3H), 4.56-4.63 (m, 1H), 5.45-5.58 (br m, 1H), 5.95 -6.08 (br m, 1H), 6.23 (s, 1H), 6.48 (s, 1H), 6.65 (s, 1H), 7.20-7.40 (m, 10H); LRMS ESI m/z 539
Example 142 5-[3-(3-Bromo-5-hvdroxv-phenoxv)-azetldln-1-yl]-5-methvl-2.2-diphenyl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product of example 141, using the same method as that described for example 114, as a colourless foam in 27% yield. 1HNMR(40QMHz, CDCI3) 6: 0.95 (s, 6H), 1.18-1.25 (m, 2H), 2.38-2.46 (m, 2H), 3.19-3.26 (m, 2H), 3.55-3.63 (m, 2H), 4.60-4.66 (m, 1H), 5.45-5.58 (br m, 1H), 6.13 (s, 1H), 6.20 -6.35 (br m, 1H), 6.48 (s, 1H), 6.65 (s, 1H), 7.20-7.35 (m, 10H); LRMS ESI m/z 525 [M+H]+*
Example 143 4-(1-t3-(3-Fluoro-4-methQXV-phenoxy)-azetldin-1-yl]-cvcloDentvlV2.2-diphenvt-butvronitrlle
(Formula Removed)
The title compound was prepared from the product of preparation 84 and 3-fluoro-4-
methoxyphenol (J. Het. Chem., 1989, 26, 1547) using a similar method to that described for
example 99, in 75% yield. .
1HNMR(400MHz, CDCI3) 5: 1.25-1.39 (m, 2H)/1.40-1.65 (m, 6H), 1.65-1.77 (m, 2H), 2.47-
2.58 (m, 2H), 3.12-3.22 (m, 2H), 3.46-3.57 (m, 2H), 3.77 (s, 3H), 4.66-4.74 (m, 1H), 6.27-6.33
(m, 1H), 6.35-6.43 (m, 1H), 6.94-7.03 (m, 1H), 7.24-7.48 (m, 10H); LRMS ESI m/z 485
[M+H]+
Example 144 4-f1-r3-(3-FluQro-4-methQXV-phenoxv)-azetidln-1-vll-cvclopentvlV2.2-diphenvl-butvramlde
(Formula Removed)
The title compound was prepared from the product of example 143, using the same method
as that described for example 100, as a colourless foam in 65% yield.
1HNMR(400MHz, CDCI3) B: 1.20-1.37 (m, 4H), 1.39-1.58 (m, 4H), 1.58-1.67 (m, 2H), 2.40-
2.53 (m, 2H), 3.06-3.15 (m, 2H), 3.46-3.53 (m, 2H), 3.75 (s, 3H), 4.60-4.71 (m, 1H), 5.50-5.67
(br m, 1H), 6.17-6.38 (m, 3H), 6.88-6.98 (m, 1H), 7.18-7.40 (m, 10H); LRMS APCI m/z 503
[M+H]+
Example 145 4-{1-T3-(3-Fluoro-4-hvdroxv-phenoxy)-azetldln-1-yl]-cvclopentvl>-2.2-diphenvl-butvramide
(Formula Removed)
The title compound was prepared from the product of example 144, using, a similar method to that described for example 114, as a colourless foam In 25% yield.
1HNMR(400MHz, CDCI3) 5: 1.31-1.47 (m, 6H), 1.48-1.62 (m, 2H), 1.64-1.78 (m, 2H), 2.43-2.54 (m, 2H), 3.27-3.37 (m, 2H), 3.76-3.85 (m, 2H), 4.75-4^84 (m, 1H), 5.44-5.58 (br m, 1H), 6.22-6.28 (m, 1H), 6.38-6.44 (m, 1H), 6.84-7.00 (m, 2H), 7.16-7.34 (m, 10H).
Example 146 S-f3-(3-Chloro-4-hvdroxv-benzvloxv)-azetldin-1-yl]-5-methvl-2.2-diphenvl-hexanoicacld amide
(Formula Removed)
The product of preparation 94 (tOOmg, 0.19mmol) was dissolved in tetrahydrofuran (10mL) and sodium borohydride (47tng, 1.2mmol) and tetrakis(triphenylphosphine)palladium(0) (22mg, 0.02mmol) were added. After stirring at 45°C for 30 minutes, the reaction was cooled to room temperature-and quenched with a few drops of glacial acetic acid. The reaction was basified with saturated sodium hydrogen carbonate solution. The organics were extracted with ethyl acetate (20mL) the organic solution was dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 95:5:0.5, afforded the title compound in 38% yield, 35mg.
1HNMR(400MHz, CDCI3) 6: 0.90 (s, 6H), 1.12-1.20 (m, 2H), 2.38-2.45 (m, 2H), 2.98-3.07 (m, 2H), 3.28-3.,39 (m, 2H), 4.06-4.15 (m, 1H), 4.26 (s, 2H), 5.53-5.65 (br m, 2H), 6.88-6.95 (m, 1H), 7.02-7.06 (m, 1H), 7.20-7.37 (m, 11H); LRMS APCl mlz 493 [M+H]+
Example 147 5-[3-((4-Chloro-2-hvdroxv-benzvLoxv)-azetidln-1-yl]-S-methvl-2.2-dlphenvl-hexanolc acid amide

(Formula Removed)
The title compound was prepared from the product of preparation 98 using a similar method to that described for example 146, in 19% yield.
1HNMR(400MHz, CDCI3) 5: 0.92 (s, 6H), 1.12-1.20 (m, 2H), 2.40-2.46 (m, 2H), 3.04-3.15 (m, 2H), 3.35-3.43 (m, 2H), 4.13-4.20 (m, 1H), 4.47 (s, 2H), 5.56-5.74 (br m, 2H), 6.75-6.80 (m. 1H), 7.03 (s, 1H), 7.08-7.14 (m, 1H), 7.23-7.38 (m, 10H); LRMS ESI m/z493 [M+H]+
Example 148
5-[3-(2-Chloro-3-hvdroxv-benzvloxv)-azetidin-1 -vl1-5-methvl-2.2-diphenvl-hexanolc acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 103 using a similar method to that described for example 128, In 25% yield.
1HNMR(400MHz, CDCI3) 6: 0.95 (s,.6H), 1.12-1.24 (m, 2H), 2.38-2.45 (m, 2H), 3.02-3.12 (m, 2H), 3.28-3.39 (m, 2H), 4.13-4.20 (m, 1H), 4.45 (s, 2H), 5.37-5.60 (br m, 2H), 6.94-6.99 (m, 2H), 7.12-7.18 (m, 1H), 7.20-7.40 (m, 10H); LRMS APCl m/z 493 [M+H]+
Example 149 5-t3-(3.5-DlhYdrQxv.phenoxyVazetldln-1-yl]-S-methvl-2ig-dlphenvl.hexanoic acid amide
(Formula Removed)
1,3,5-trihydroxybenzene dihydrate (10g, 79mmol) was placed in a round bottomed flask equipped with a Dean Stark trap and dehydrated using 23mL toluene. After removal of the water and concentration in vacuo, the dry phenol was isolated as a white solid. A mixture of caesium carbonate (107mg, 0.33mmol) and anhydrous 1,3,5-trihydroxybenzene (125mg, 0.99mmol) in N.N-dimethylformamide (3mL) was stirred at 80°C for 10 minutes. The product of preparation 104 (142mg, 0.33mmol) was added and the reaction mixture was stirred at 80°C for 10 minutes. The crude material was partitioned between ethyl acetate (20mL) and water (30mL), the organic layer was separated and the aqueous re-extracted with ethyl acetate (2x20mL), The combined organlcs were dried over magnesium sulphate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with pentane: (90:10:1 ethyl acetate:methanol:0.88 ammonia), 100:1 to 30:70, to afford the title compound as a colourless gum in 5% yield, 7mg.
1HNMR(400MHz, CDCI3) 5: 0.95 (s, 6H), 1.20-1.28 (m, 2H), 2.35-2.48 (m, 2H), 3.15-3.24 (m, 2H), 3.52-3.60 (m, 2H), 4.48-4.58 (m, 1H), 5.62-5.65 (br s, 1H), 5.78 (s, 2H), 6.06 (s, 1H), 6.35-6.40 (br s, 1H), 7.15-7.28 (m, 10H); LRMS APCI m/z 461[M+H]+
Example 150 5-[3-(3-Hvdroxv-phenoxv)-azetidin-1-yl]-S-methvl-2.2-diphehvl-hexanenitrile
(Formula Removed)
The title compound was prepared from the product of preparation 105, using the same method as that described in example 109, as a colourless oil in 73% yield. 1HNMR(400MHz, CDCI3) 5: 0.98 (s, 6H), 1.35-1.40 (m, 2H), 2.42-2.48 (m, 2H), 3..16-3.22 (m, 2H), 3.45-3.57 (m, 2H), 4.64-4.72 (m, 1H), 6.25 (s, 1H), 6.30-6.35 (m, 1H), 6.42-6.48 (m, 1H), 7.05 -7.15 (m, 1H), 7.25-7.42 (m, 10H); LRMS APCI m/z 427 [M+H]+
Example 151
(Formula Removed)
5(3-f(4-Hvdroxvbenzvl^xv1azetidln-1-vft-5-methvl-2.2-dlphenvlh6xanenltri!a CH9
The title compound was prepared from the products of preparations 56 and 66, using the same method as that described for example 101, in 15% yield.
1HNMR(400MHz, CDCI3) 6:0.95(s, 6H), 1.32-1.40(m, 2H), 2.40-2.48(m, 2H), 3.04-3.08(m, 2H), 3.26-3.35(m, 2H), 4.05-4.15(m, 1H), 4.32(s, 2H), 6.72-6.76(m, 2H), 7.10-7.15(m, 2H), 7.18-7.46(m, 10H)
Example 152 5-[3-(4-Hvdroxv-benzvloxv)-azetldin-1-yl]-S-methvl-2.2-d'iphenvl-hexanoic acid amide
(Formula Removed)
The title compound was prepared from the product of preparation 108 using a similar method to that described for example 146, in 53% yield.
1HNMR(400MHz, MeOD) 5: 0.95 (s, 6H), 1.23-1.28 (m, 2H), 2.35-2.45 (m, 2H), 2.96-3.05 (m, 2H), 3.22-3.28 (m, 2H), 4.01-4.18 (m, 1H), 4.30 (s, 2H), 5.55-5.65 (br s, 2H), 6.70-6.75 (m, 2H), 7.05-7.12 (m, 2H), 7.20-7.35 (m, 10H); LRMS ESI m/z 459 [M+H]+
Potency assay
M3 potency was determined in CHO-K1 cells transfected with the NFAT-Betalactamase gene.
CHO (Chinese Hamster Ovary) cells recombinantly expressing the human muscarinic M3
receptor were transfected with the NFATJJ-Lac_Zeo plasmid. Cells were grown in DMEM
with Glutamax-1, supplemented with 25mM HEPES(Life Technologies 32430-027), containing
10% PCS (Foetal Calf Serum; Sigma F-7524), 1nM Sodium pyruvate (Sigma S-8636), NEAA
(non-Essential Amino Acids; Invitrogen 11140-035) and 200ng/ml Zeocln (Invitrogen R250-
01).
hMa B-Lac Assay Protocol
Cells were harvested for assay when they reached 80-90% confluency using enzyme free cell
Dissociation Solution (Life technologies 13151-014) incubated with the cells for 5 min at 37°C
in an atmosphere containing 5% CO2. Detached cells were collected in warmed growth
media and centrifuged at 2000rpm for 10min, washed in PBS (Phosphate Buffered Saline; Life Technologies 14190-094) and centrifuged again as just described. The cells were re-suspended at 2x105 cells/ml in growth medium (composition as described above). 20jj,l of this cell suspension was added to each well of a 384 well black clear bottomed plate (Greiner Bio One 781091-PFI). The assay buffer used was PBS supplemented with 0.05% Pluronic F-127 (Sigma 9003-11-6) and 2.5% DMSO. Muscarinic M3 receptor signalling was stimulated using 80nM carbamyl choline (Aldrich N240-9) incubated with the ceils for 4h at 37°C /5% C02 and monitored at the end of the incubation period using a Tecan SpectraFluor* plate reader (X -excitation 405nm, emission 450nm and 503nm). Ma receptor antagonists under test were added to the assay at the beginning of the 4h Incubation period and compound activity measured as the concentration dependent inhibition of the carbamyl choline induced signal. Inhibition curves were plotted and IC50 values generated using a 4-parameter sigmoid fit and converted to Ki values using the Cheng-Prusoff correction and the KD value for carbamyl choline In the assay.
It has thus been found that carboxamide derivatives of formula (I) according to the present invention that have been tested in the above assay show Ms receptor antagonist activity as listed in the table below:

(Table Removed)
Guinea Pig Trachea assay
Male, Dunkin-Hartley guinea-pigs weighing 350-450g are culled in a rising concentration of C02, followed by exsanguinations of the vena cava. Tracheas are dissected from the larynx to the entry point into the chest cavity and then placed in fresh, oxygenated, modified Krebs buffer solution (Krebs containing 10uM propranolol, 10uM guanethidine and 3uM indomethacin) at room temperature. The tracheas are opened by cutting through the cartilage opposite the trachealis muscle. Strips approximately 3-5 cartilage rings wide are cut. A cotton thread is attached to the cartilage at one end of the strip for attachment to the force transducer and a cotton loop made at the other end to anchor the tissue In the organ bath. The strips are mounted In 5ml organ baths filled with warm (37°C) aerated modified Krebs. The pump flow rate is set to 1.0 ml/ mln and the tissues washed continuously. Tissues are placed under an initial tension of 1000mg. Tissues are re-tensioned after 15 and 30 minutes, then allowed to equilibrate for a further 30-45 minutes.
Tissues are subjected to electrical field stimulation (EPS) of the following parameters: 10s trains every 2 minutes, 0.1ms pulse width, 10Hz and 10-30V. The voltage is raised 5V every 10min within the stated range until a maximum contractile response for each tissue is observed. This just maximum voltage for each tissue is then used throughout the remainder of the experiment. Following equilibration to EPS for 20min, the pump is stopped, and after 15min control readings are taken over a 8-10 min period (4-5 responses). Compound-is then added to each tissue as a bolus dose at 30xKi (determined at the human M3 receptor expressed in CHO cells in a filtration binding assay), and left to incubate for 2h. Compound is then washed from tissues using a rapid wash with modified Krebs for 1min and flow Is restored to 1 ml/min for the remainder of the experiment. At the end of the experiment tissues are challenged with histamine (1nM) to determine viability. Readings taken during the
experiment are automatically collected using Notocord ® software. The raw data are converted into percent response taking into account measurements of inhibition of the EPS response. After starting washout, the times taken for the tissue to recover by 25% from the inhibition induced are recorded and used as a measure of compound duration of action. Tissue viability limits the duration of the experiment'to 16h post-compound washout. Compounds are typically tested at n=2 to 5 to estimate duration of action.
Alternatively the following Guinea Pig Trachea assay can also be used:
Trachea were removed from male Dunkin-Hartley guinea-pigs (wt 350-450g) and following removal of adherent connective tissue, an incision was made through the cartilage opposite the trachealis muscle and trachea! strips 3-5 cartilage rings wide prepared. The tracheal strips were suspended between an isometric strain gauge and a fixed tissue hook with the muscle in the horizontal plane in 5ml tissue baths under an Initial tension of 1g and bathed in warmed (37°C) aerated (95%O2/5%CO2) Krebs solution containing 3uM indomethacin and 10nM guanethidine. The tissues were positioned between parallel platinum wire electrodes (~1cm gap). A constant 1ml/mln flow of fresh Krebs solution (of the above composition) was maintained through the tissue baths using peristaltic pumps. The tissues were allowed to equilibrate for an hour with re-tensioning to 1g at 15min and 30min from the start of the equilibration period. At the end of the equilibration, tissues were electrically, field stimulated (EPS) using the following parameters: 10V, 10Hz 0.1ms pulse width with 10sec trains every 2 min. In each tissue a voltage response curve was constructed over the range 10v - 30V (keeping all other stimulation parameters constant) to determine a just maximal stimulation. Using these stimulation parameters EPS responses were 100% nerve mediated and 100% cholinergic as confirmed by blockade by 1uM tetrodotoxin or \\M atropine. Tissues were then repeatedly stimulated at 2 min intervals until the responses were reproducible. The peristaltic pump was stopped 20 min prior to the addition of the study compound and the average twitch contraction over the last 10min recorded as the control response. The study compound was added to the tissue baths, with each tissue receiving a single concentration of compound and allowed to equilibrate for 2h. At 2h post addition the inhibition of the EPS response was recorded and IC50 curves generated using a range of compound concentrations over tracheal strips from the same animal. The tissues were then rapidly washed and the 1ml/min perfusion with Krebs solution re-established. Tissues were stimulated for a further 16h and recovery of the EPS response recorded. At the end of the 16h, 10jiM histamine was added to the baths to confirm tissue viability. The just max concentration (tested concentration giving a response > 70% inhibition but less than 100%) of antagonist was identified from the 1C50 curve and the time to 25% recovery of the induced inhibition (T2e) calculated in tissues receiving this concentration. Compounds are typically tested at n=2 to 5 to estimate duration of action.





We claim
1. A compound of formula (I)
wherein,
- R' is CN or CONH2
- A is selected from
wherein * and ** represent the attachment points, ** being linked to the oxygen,
- R2 and R3 are methyl or where A is a group of formula
R2 and R3 may also together form with the carbon atom to which they are linked a
cyolopentane ring;
- p i s o o r 1;
- A' is selected from
a) phenyl optionally substituted with 1, 2 or 3 groups independently selected from
halo, CN, CF3, 0R4, sR4, OCF3, (C1-C4)alkyl and phenyl optionally substituted
with OH;
b) naphthyl optionally substituted with 1 or 2 groups selected from halo, CN, CF3,
OR^, SR~O, CF3 and (CI-C4)alkyl;
c) a 9 or 10-membered bicyclic aromatic heterocyclic group, containing from 1,2 or
3 heteroatoms independently selected from 0 , S or N, said heterocyclic group
being optionally substituted with 1 or 2 substituents independently selected from
OR^, (C1- C4)alkyl and halo;
- R~ is H or (C1-C4)alkyl;
or, if appropriate, the pharmaceutically acceptable salts or solvates thereof.
A compound as claimed in claim 1 where R' is CONH2.
A compound as claimed in claim 1 or 2 where p is 0.
A compound ,as claimed in claim 1 or 2 where p is 1.
A compound as claimed in any one of claims 1 to 4 where A' is phenyl optionally
substituted with 1, 2 or 3 groups, independently selected from F, C1, CF3, OH, OCH3,
OCF3 and CH3.
A compound as claimed in any one of claims 1 to 5 where A' is phenyl optionally
substituted with 1 or 2 groups independently selected from F, C1, CF3, OH, OCH3, OCF3
and CH3.
A compound as claimed in any one of claims 1 to 4 where A' is naphthyl optionally
substituted with OH.
A compound as claimed in one of claims 1 to 4 where A' is selected from indolyl,
isoindolyl, quinolyl, isoquinolyl, benzofuranyl, isobenzofuranyl, benzothienyl,
isobenzothienyl, quinazolyl, quinoxalyl, phthalazinyl, benzothiazolyl, benzoxazolyl,
benzisothiazolyl, benzisoxazolyl, benzimidazolyl, indazolyl, benzotriazolyl,
benzoxadiazolyl, benzisoxadiazolyl, benzothiadiazolyl and benzisothiadiazolyl.
A compound as claimed in any one of claims 1 to 4 wherein A' is benzoxazolyl.
10. A compound as claimed in any one of claims 1 to 9 where R2 and R3 are methyl.
11. A compound as claimed in any one of claims 1 to 10 where A is a group of formula
12. A compound as claimed in any one of claims 1 to 10 where A is a group of formula
13. A compound as claimed in any one of claims 1 to 10 where A is a group of formula
14. A compound as claimed in claim 1, said compound being selected from:
5-Methyl-5-[(3S)-3-phenoxypyrrolidin-I -yl]-2,2-diphenylhexanamide;
5-Methyl-5-[(3R)-3-phenoxypyrrolidin-l-yl]-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Hydroxyphenoxy)pyrrolidin-I -yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(3-Hydroxyphenoxy)pyrrolidin-1-y l]-5-methyl-2,2-diphenylhexanamide;
5-[(3S)-3-(3-Fluoro-5-Hydroxy-phenoxy)-pyrrolidin-l-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3S)-3-(2-Fluoro-3-Hydroxy-phenoxy)-pyrrolidin-l-yl]-5-methyl-2,2-diphenyl-hexanoic acid
amide;
5-[(3R)-3-(2-Fluoro-3-hydroxy-phenoxy)-pyrrolidin-l -yl]-5-methyl-2,2-diphenylhexanamide;
5-[(3R)-3-(2-Chloro-3-hydroxy-phenoxy)-pyrrolidin-l -yl]-5-methyl-2,2-diphenylhexanamide;
5-Methyl-5-(4-phenoxypiperidin-1 -yl)-2,2diphenylhexanamide;
5-[4-(3-hydroxyphenoxy)piperidin-1 -yl]-5-methyl-2,2diphenylhexanamide;
5-Methyl-5-(3-phenoxyazetidin-1 -yl)-2,2diphenyl hexanamide;
5-[3-(3-Hydroxyphenoxy)azetidin-l-yl]-5-methyl-2,2-diphenylhexanamide;
543-(4-Chloro-3-hydroxy-phenoxy)-azetidin-1 -yl)-5-methyl-2,2-diphenylhexanamide;
5-(3-(3-Fluoro-5-hydroxy-phenoxy)-azetidi- -yl}-5-methyl-2,2-diphenyihexanamide;
5-(3-(3-Chloro-5-hydroxy-phenoxy)-azetidin-I -yl}-5-methyl-2,2-diphenylhexanamide;
4 5-[3-(2-Fluoro-3-hydroxy-phenoxy)-azetid- -yl]S-methyl-2,2-diphenyl-hexanoic acid amide;
5-~3-(2-Fluoro-5-hydroxy-phenoxy)-azetidin-l-yl]-5-methyl-2,2-diphenyl-hexanoic acid amide;
and,
5-[3-(4-Ch~oro-3-hydroxy-benzyloxy)-azetidin-1-yij-5-methyl-2,2-diphenyl-heaxcaidno almc ide
or, if appropriate, the pharmaceutically acceptable salts or solvates thereof of the kind
such as herein described.
15. A compound as claimed in claim 1, said compound being 5-[3-(3-
Hydroxyphenoxy)azetidin- 1-yl]-5-methyl-2,2-diphenylhexanamidoer a pharmaceutically
acceptable salt or solvate thereof of the kind such as herein described.
16. A pharmaceutical composition comprising at least an effective amount of a compound of
the formula (I) as claimed in any one of claims 1 to 15 or a pharmaceutically acceptable
salts or solvates thereof of the kind such as herein described.
17. A compound of the formula (I) as claimed in any one of claims 1 to 15 or a
pharmaceutically acceptable salts or solvates thereof, for use as a medicament.
Dated this 11" day of March, 2008
ATTORNEY FOR THE APPLICANTS

Documents:

2087-delnp-2008-2087-delnp-2008-Correspondence Others-(07-01-2013).pdf

2087-delnp-2008-2087-delnp-2008-Form-3-(07-01-2013).pdf

2087-delnp-2008-2087-delnp-2008-GPA-(07-01-2013).pdf

2087-delnp-2008-2087-delnp-2008-Petition-137-(07-01-2013).pdf

2087-delnp-2008-abstract.pdf

2087-delnp-2008-Claims- (11-07-2013).pdf

2087-delnp-2008-claims.pdf

2087-delnp-2008-Correspondence Others-(13-08-2008).pdf

2087-delnp-2008-Correspondence-others (11-07-2013).pdf

2087-delnp-2008-correspondence-others.pdf

2087-delnp-2008-description (complete).pdf

2087-delnp-2008-form-1.pdf

2087-delnp-2008-Form-18-(13-08-2008).pdf

2087-delnp-2008-form-2.pdf

2087-delnp-2008-form-3.pdf

2087-delnp-2008-form-5.pdf

2087-delnp-2008-gpa.pdf

2087-delnp-2008-pct-210.pdf

2087-delnp-2008-pct-237.pdf

2087-delnp-2008-pct-304.pdf

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Patent Number 256758
Indian Patent Application Number 2087/DELNP/2008
PG Journal Number 30/2013
Publication Date 26-Jul-2013
Grant Date 25-Jul-2013
Date of Filing 11-Mar-2008
Name of Patentee PFIZER INC.
Applicant Address RAMSGATE ROAD, SANDWICH, KENT, CT13 9NJ,U.K.
Inventors:
# Inventor's Name Inventor's Address
1 PAUL ALAN GLOSSOP RAMSGATE ROAD, SANDWICH, KENT, CT13 9NJ,U.K
2 SIMON JOHN MANTELL PFIZER GLOBAL RESEARCH AND DEVELOPMENT, RAMSGATE ROAD, SANDWICH, KENT, CT13 9NJ,U.K
3 ROSS SINCLAIR STRANG PFIZER GLOBAL RESEARCH AND DEVELOPMENT, RAMSGATE ROAD, SANDWICH, KENT, CT13 9NJ,U.K
4 ANTHONY WOOD PFIZER GLOBAL RESEARCH AND DEVELOPMENT, RAMSGATE ROAD, SANDWICH, KENT, CT13 9NJ,U.K
5 CHRISTINE ANNE LOUISE WATSON PFIZER GLOBAL RESEARCH AND DEVELOPMENT, RAMSGATE ROAD, SANDWICH, KENT, CT13 9NJ,U.K
PCT International Classification Number C07D 207/12
PCT International Application Number PCT/IB2006/002727
PCT International Filing date 2006-09-01
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/719,477 2005-09-21 U.S.A.
2 60/719,468 2005-09-21 U.S.A.