Title of Invention

"A CYCLIC AMINE DERIVATIVE OR SALT THEREOF AND ITS PHARMACEUTICAL COMPOSITION"

Abstract Disclosed herein arc novel benzoimidazole derivatives functioning as antagonists to vanilloid receptor-1, and a pharmaceutical composition comprising the same. They arc useful in preventing or treating pain, acute pain, chronic pain, neuropathic pain, postoperative pain, migraines, arthralgia, neuropathy, nerve injury, diabetic neuropathy, neurological illness, neurodermatitis, strokes, bladder hypersensitivity, irritable bowel syndrome, respiratory disorders such as asthma, chronic obstructive pulmonary disease, etc., burns, psoriasis, itching, vomiting, irritation of the skin, eyes, and mucous membranes, gastric-duodenal ulcers, inflammatory intestinal diseases, and inflammatory diseases.
Full Text DESCRIPTION
CYCLIC AMINE DERIVATIVE AND SALT THEREOF
TECHNICAL FIELD
[0001]
The present invention relates to a cyclic amine derivative and its salt useful as
medicines, especially as NMDA receptor antagonists, and to an NMDA receptor antagonist
comprising it as the active ingredient thereof. The cyclic amine derivative and its salt and
the NMDA receptor antagonist comprising it as an active ingredient according to the
present invention are useful for treatment and prevention of Alzheimer's disease,
cerebrovascular dementia, Parkinson's disease, ischemic apoplexy, pain, etc.
BACKGROUND ART
[0002]
Glutamic acid acts as a neurotransmitter in the central nervous system of
mammals, and it controls the activity of neurocytes or the release of neurotransmitters via
the glutamate receptor existing in synapses. At present, the glutamate receptor is
classified into an "ion-channel glutamate receptor" and a "metabotropic glutamate receptor"
from many physiological.and biological studies (Hollmann M. and Heinemann S., Annu.
Rev. Neurosci., 17 (1994) 31-108). NMDA (N-methyl-D-aspartate) receptor is an ionchannel
glutamate receptor specifically sensitive to the agonist NMDA (Moriyoshi K. et al.,
Nature, 354 (1991) 31-37; Meguro H. et al., Nature, 357 (1992) 70-74); and this has high
Ca2+ permeability (lino M. et al., J. Physiol., 424 (1990) 151-165). NMDA receptor is
expressed with a specific pattern in a central nervous system (Ozawa S. et al., Prog.
Neurobiol., 54 (1998) 581-618).
From many pharmacological and biological studies, it is considered that NMDA
receptor may participate in high-order neurologic functions such as memory and learning
pis RG., et al, Nature, 319 (1986) 774-776; Tsien JZ. et al., Cell, 87 (1996) 1327-
1338). On the other hand, it is suggested that acute or chronic NMD A receptor
hyperactivity or hypoactivity may participate in various nervous system diseases, for
example, ischemic apoplexy, hemorrhagic brain injury, traumatic brain injury,
neurodegenerative disorders (e.g., Alzheimer's disease, cerebrovascular dementia,
Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis), glaucoma, AIDS
encephalopathy, dependence, schizophrenia, depression, mania, stress-related diseases,
epilepsy, pain (Beal MF., FASEB J., 6 (1992) 3338-3344; Heresco-Levy U. and Javitt DC.,
Euro. Neuropsychopharmacol., 8 (1998) 141-152; Hewitt DJ., Clin. J. Pain, 16 (2000) S73-
79). Accordingly, drugs capable of controlling the activity of NMD A receptor would be
extremely useful in clinical application.
[0003]
As drugs capable of controlling the activity of NMD A receptor, a large number of
non-competitive NMDA receptor antagonists are reported, but many of them are not as yet
used in clinical application because of their side effects based on the NMDA receptorantagonizing
effect thereof, for example, mental aberration such as hallucination or
confusion, or giddiness. Some already-existing NMDA receptor antagonists, for example,
ketamine and dextromethorphan have been tried for pain in clinical application (Fisher K.
et al., J. Pain Symptom Manage., 20 (2000) 358-373), but the safety margin in the treatment
with them is narrow and their clinical use is limitative (Eide PK., et al., Pain, 58 (1994)
347-354). Memantine is known as a non-competitive NMDA receptor antagonist that has
comparatively few side effects (Parsons CO., et al., Neuropharmacol., 38 (1999) 735-767);
and recently, it has been reported that this may be effective for Alzheimer's disease
(Reisberg B., et al., N. Engl. J. Med., 348 (2003) 1333-1341). However, the safety margin
of memantine as a medicine is still not satisfactory, and an NMDA receptor antagonist
having a broader safety margin is desired (Ditzler K., Arzneimittelforschung, 41 (1991)
773-780; Maier C., et al., Pain, 103 (2003) 277-283; Riederer P., et al., Lancet, 338 (1991)
1022-1023). It is expected that the creation of such an NMDA receptor antagonist having
a bj^sder safety margin may bring about new clinical usefulness of the NMD A receptor
antagonist.
[0004]
Patent Reference 1 describes a pharmaceutical composition for prevention and
treatment of cerebral ischemia, which comprises an adamantane derivative of the following
formula or its pharmaceutically-acceptable acid-addition salt.
(wherein RI and RZ are the same or different, each representing a hydrogen atom, or a linear
or branched alkyl group having from 1 to 6 carbon atoms, or the like; RS and R4 are the
same or different, each representing a hydrogen atom, or an alkyl group having from 1 to
carbon atoms, or the like; RS represents a hydrogen atom, or a linear or branched alkyl
group having from 1 to 6 carbon atoms; for the details of the symbols in the formula, the
patent publication is referred to).
In Patent Reference 1, the above-mentioned memantine is described as Test
Compound No. 1 (memantine is a compound of the formula where RI, R2 and Ra are
hydrogen atoms, and R4 and RS are methyl groups).
[0005]
Patent Reference 2 describes 1-amino-alkylcyclohexane of the following formula
as an NMDA receptor antagonist.
(wherein R* is -(CH2)n-(CR6R7)m-NR8R9; n + m = 0,1 or 2; R sndentiy
selected from a group consisting of a hydrogen atom and a Ci.6 lower alkyl group, and at
least R1, R4 and R5 are lower alkyl groups; for the details of the symbols in the formula, the
patent publication is referred to).
[0006]
Patent Reference 3 describes an indane derivative of the following formula,
which is a type of a compound having an indane ring and a piperidine ring, and useful as a
treating agent for allergy and asthma.
(wherein RI and R2 each independently represent a CM alkyl group; RS represents a
hydrogen atom, a CM alkyl group, a C1-4 alkoxy group, or the like; and the ring A may
have a substituent; for the details of the symbols in the formula, the patent publication is
referred to).
However, in the compound described in this reference, the indane ring and the
piperidine ring are bonded to each other via a double bond therebetween, and the structure
of the compound differs from that of the compound of the present invention in that in the
latter, the two rings are bonded to each other via a single bond or a lower alkylene group,
etc. In addition, the compound described in the reference is useful as a treating agent for
allergy and asthma, but the reference does neither disclose nor suggest the NMDA receptorantagonizing
effect of the compound and the usefulness of the compound as a treating agent
for Alzheimer's disease, cerebrovascular dementia, Parkinson's disease, ischemic apoplexy,
pain, etc. In Example 1 in this reference, described is 6-chloro-2,2-dimethyl-l-(l-methyl-
4-piperidinyl)indan-l-ol of the following formula, as an intermediate for producing the
ed compound. However, this reference discloses nothing relating to the use of the
intermediate for medicine.
[0007]
Non-Patent Reference 1 describes a compound of the following formula, which is
a type of a compound having an indane ring or a tetrahydronaphthalene ring and a
piperidine ring, and may be used as an analgesic agent. However, the structure of this
compound differs from that of the compound of the present invention described(0
(Figure Removed)
hereinunder, in that in the former, the saturated ring is substituted with a phenyl group. (wherein R represents a hydrogen atom, or a methyl group; R' represents a methyl group;
R" represents -(CH2)3N(CH3)2, -(CHa^NCCHaXC^^CeHs, an N-methyl-piperidyl group,
(CH2)2N(CH3)2; n indicates 0 or 1; for the details of the symbols in the formula, the patent
publication is referred to).
Patent Reference 1: Japanese Patent No. 2821233,
Patent Reference 2: WO 99/01416,
Patent Reference 3: JP-A 56-135472,
Non-Patent Reference 1: Journal of Medicinal Chemistry, 1967, Vol. 10, No. 5, pp. 823-
825.
DISCLOSURE OF THE INVENTION
PROBLEMS THAT THE INVENTION IS TO SOLVE
[0009]
With the increase in the old age population, cases of Alzheimer's disease,
cerebrovascular dementia, ischemic apoplexy and the like are increasing these days; and it
is earnestly desired in the field of medicine to create an NMDA receptor antagonist which
is effective for treatment and prevention of such diseases as well as Parkinson's disease,
pain and others and has a broader safety margin. An object of the present invention is to
provide a novel cyclic amine derivative and its salt having an excellent NMDA receptor
antagonistic activity and having a broader safety margin, and to provide a pharmaceutical
composition containing it.
MEANS FOR SOLVING THE PROBLEMS
[0010]
The present inventors have found that a novel amine derivative and its salt [1]
represented by the following formula (I), which is characterized in that the aminecontaining
structure A therein bonds to a 2-cyclic or 3-cyclic condensed ring (e.g., indane,
tetralone, 4,5,6,7-tetrahydrobenzothiophene, 4,5,6,7-tetrahydrobenzoruran, 7,8-dihydro-6Hindeno[
4,5-b]furan, 2,3-dihydro-lH-cyclopenta[a]naphthalene) viaX1 (e.g., bond or lower
alkylene), have an excellent NMDA receptor antagonistic activity and a broad safety
margin, and have completed the present invention. Specifically, the present invention
rel|te$ to an amine derivative of the following formula (I) and its salt (hereinafter this may
be referred to as "the compound (I) of the present invention"). Further, the present
invention also relates to an NMDA receptor antagonist comprising the compound (I) or its
salt of the present invention, especially a treating agent or a preventing agent for
Alzheimer's disease, cerebrovascular dementia, ischemic apoplexy, pain, etc. In the
present invention, the compounds of the following [2] are preferred, and the compounds of
the following [3] are more preferred. The compounds of [4] are most preferred.
[0011]
[1] A cyclic amine and its salt of the following formula (I):
(wherein the symbols have the following meanings:
A: a 5- to 8-membered cyclic amine optionally havhig a double bond, optionally having a
bridge structure and optionally having a substituent of R7 to R11 in the ring, or
-NH2, -NH(lower alkyl), or -N(lower alkyl)2;
Ring B: benzene, thiophene, furan, pyrrole, a 5- to 7-membered cycloalkane, or a 5- to 7-
membered cycloalkene;
X1: a bond, a lower alkylene, or -L3-D-L4-;
L3 and L4: the same or different, and a bond or a lower alkylene;
D: a 5- or 6-membered carbon ring or hetero ring optionally having a substituent;
X2: -(CR12R13)n-, -N(R14)-, -N(R14)CO-, -CON(R14)-, -O-, -S-, -CO-, -CH(OH)-,
-N(R14)-(CR12R13)n-, -(CR12R13)n-N(R14)-, -CON(R14)-(CR12R13)n-, -N(R14)CO-
(CR12R13)n-, -(CR12R13)n-N(R14)CO-, -(CR12R13)n-CON(R14)-, -CO-(CR12R13)n-,
-(CR12R13)n-CO-, -0-(CR12R13)n-, -(CR12R13)n-O, -S-(CR12R13)n-, or -(CR12R13)n-S-;
YOH, -O-lower alkyl, -NH2, or -N3;
R1 and R2: the same or different, and a halogen atom, a lower alkyl, or a lower alkylene-
R3 to R6: the same or different, and a hydrogen atom, a halogen atom, a lower alkyl, a lower
alkenyl, a lower alkynyl, -O-lower alkyl, -OH, -NH2, -NH(lower alkyl), -N(lower alkyl)2,
-NH-CO-lower alkyl, -N(lower alkyl)-CO-lower alkyl, -NH-CO-0-lower alkyl, -NQower
alkyl)-CO-O-lower alkyl, -CN-, -NO2, -CF3, -lower alkylene-OH, -lower alkylene-halogen
atom, -O-lower alkylene-OH, -lower alkylene-O-lower alkyl, -CO-N(lower alkyl)2, -CONH-(
lower alkyl), -O-CO-N(lower alkyl)2, -O-CO-NH-(lower alkyl), a 5- to 8-membered
cyclic amine, -CO-5- to 8-membered cyclic amine, -COOH, -COO-lower alkyl, -COOlower
alkylene-aryl, a 5- or 6-membered hetero ring, -lower alkylene-5- or 6-membered
hetero ring, an aryl optionally having a substituent, or an aryl optionally having -lower
alkylene-substituent;
R7: a hydrogen atom, a lower alkyl, -lower alkylene-aryl, or -lower alkylene-heteroaryl:
R7 is a substituent on the nitrogen atom of the cyclic amine;
R8 to R14: the same or different, and a hydrogen atom, or a lower alkyl;
n: an integer of 1, 2 or 3;
wherien R5 and R6, R4 and R5, or R3 and R4 may together form a lower alkylene, -O-lower
alkylene-O-, -O-lower alkylene-, -lower alkylene-O-, -S-lower alkylene-, -lower alkylene-
S-, -N(R19)-lower alkylene-, -lower alkylene-N(R19)-, -C(R15)=C(R16)-0-, -OC(
R15)=C(R16)-, -C(R15)=C(R16)-C(R17)=C(R18)-, -S-C(R15)=C(R16)-, -C(R15)=C(R16)-S-,
-N(R19)-C(R15)=C(R16)-, -C(R15)=C(R16)-N(R19)-, -N(R19)-C(R15)=N-, -N=C(R15)-N(R19)-,
-N=C(R15)-C(R16)=C(R17)-, -C(R15)=C(R16)-C(R17)=N-, -C(R15)=N-C(R16)=C(R17)-, or
-C(R15)=C(R16)-N=C(R17)-; R3 and Y1 may together form -O-lower alkylene-O-, -lower
alkylene-O-, or -N(R19)-lower alkylene-O-; R1 and Y1 may together form -lower alkylene-
O-;and Y1 and the branch on -X!-A may together form -O-, or -O-lower alkylene;
R to R : the same or different, and a hydrogen atom, a halogen atom, or a lower alkyl
group;
R1^shydrogen atom, or a lower alkyl group;
provided that 6-chloro-2,2-dimethyl-l-(l-methyl-4-piperidinyl)indan-l-ol is excluded from
the compound).
[2] A cyclic amine derivative and its salt of the following formula (II):
(wherein the symbols have the following meanings:
Ring A: a 5- to 7-membered cyclic amine optionally having a double bond in the ring;
Ring B: benzene, thiophene, furan, pyrrole, a 5- to 7-membered cycloalkane, or a 5- to 7-
membered cycloalkene;
X1: a bond, or a lower alkylene;
X2: -(CR12R13)n-, -N(R14)-, -N(R14)CO-5 -CON(R14)-, -O-, -S-, -CO-, -N(R14)-(CR12R13)n-,
-(CR12R13)n-N(R14)-,-CON(R14)-(CR12R13)n-,-N(R14)CO-(CR12R13)n-,
-(CR12R13)n-N(R14)CO-, -(CR12R13)n-CON(R14)-, -CO-(CR12R13)n-, -(CR12R13)n-CO-,
-0-(CR12R13)n-, -(CR12R13)n-0-, -S-(CR12R13)n-, or -(CR12R13)n-S-;
Y1: -OH, -O-lower alkyl, -NH2, or -N3;
R1 and R2: the same or different, and a halogen atom, or a lower alkyl;
R to R : the same or different, and a hydrogen atom, a halogen atom, a lower alkyl, -Olower
alkyl, -OH, -CN, or -CF3;
R7: a hydrogen atom, a lower alkyl, -lower alkylene-aryl, or -lower alkylene-heteroaryl:
R to R : the same or different, and a hydrogen atom, or a lower alkyl;
provided that 6-chloro-2,2-dimethyl-l-(l-methyl-4-piperidinyl)indan-l-ol is excluded from
the compound).
[0013]
[3] A cyclic amine and its salt of the following formula (III):
(wherein the symbols have the following meanings:
X1: a bond, or a lower alkylene;
Y1: -OH, -O-lower alkyl, -NH2 or -N3;
R1 and R2: the same or different, and a halogen atom, or a lower alkyl;
R3 to R6: the same or different, and a hydrogen atom, a halogen atom, a lower alkyl, -0-
lower alkyl, -OH, -CN, or -CF3;
R7: a hydrogen atom, a lower alkyl, -lower alkylene-aryl, or -lower alkylene-heteroaryl;
R to R11: the same or different, and a hydrogen atom, or a lower alkyl;
provided that 6-chloro-2,2-dimethyl-l-(l-methyl-4-piperidinyl)indan-l-ol is excluded from
the compound).
[0014]
[4] The compound and its salt of [1], selected from 2,2-dimethyl-l-(lmethylpiperidin-
4-yl)indan-1 -ol, 2,2,6-trimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 6-
fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 5-bromo-2,2-dimethyl-1 -(1
methylpiperidin-4-yl)indan-1 -ol, 6-chloro-5 -fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-
yl)indan-1 -ol, 6-bromo-4-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 7-
broffiD'6-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 7-bromo-4-fluoro-2,2-
dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 6-fluoro-7-methoxy-2,2-dimethyl-1 -(1
methylpiperidin-4-yl)indan-1 -ol, 4-fluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-
yl)indan-1 -ol, 2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-1,2,3,4-tetrahydronaphthalen-1 -ol,
4-fluoro-6-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 7-ethoxy-6-fluoro-
2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 4-fluoro-6,7-dimethoxy-2,2-dimethyl-
1 -(1 -methylpiperidin-4-yl)indan-1 -ol, 5,6-difluoro-7-methoxy-2,2-dimethyl-1 -(1 -
methylpiperidin-4-yl)indan-1 -ol, 6-cyano-4-fluoro-7-methoxy-2,2-dimethyl-1 -(1 -
methylpiperidin-4-yl)indan-l-ol, l-(2-amino-2-methylpropyl)-2,2,6-trimethylindan-l-ol, 5-
fluoro-7,7-dimethyl-8-(l-methylpiperidin-4-yl)-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-
8-ol, 4-(9-fluoro-5,5-dimethyl-2,3,5,6-tetrahydro-4aH-indeno[ 1,7-ef] [ 1,4]dioxepin-4a-yl-1 -
methylpiperidine, l-[(6l-fluoro-7l-methoxy-2',2'-dimethyl-2l,3l,4,5-tetrahydro-3Hspiro
[furan-2,1 '-inden]-5 -yl)methyl]pyrrolidine.
EFFECT OF THE INVENTION
[0015]
The compounds of the present invention have an NMDA receptor antagonistic
activity and are useful for treatment and prevention of Alzheimer's disease, cerebrovascular
dementia, Parkinson's disease, ischemic apoplexy, pain.
BEST MODE FOR CARRYING OUT THE INVENTION
[0016]
The present invention is described concretely hereinunder.
Unless otherwise specifically indicated, the term "lower" used in the definition of
the formulae in this description means a linear or branched carbon chain having from 1 to
carbon atoms. Accordingly, "lower alkyl" is preferably a linear or branched d-6 alkyl
group, including, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl,
tertJgptyl, pentyl, isopentyl, hexyl, isohexyl. Of those, preferred are the groups having
from 1 to 3 carbon atoms; and more preferred are methyl and ethyl.
"Lower alkylene" includes methylene, ethylene, propylene, butylene, and also
other branched lower alkylene groups. Preferred are lower alkylene groups having from 1
to 3 carbon atoms; more preferred are methylene and ethylene; and even more preferred is
methylene.
"Halogen atom" includes a fluorine atom, a chlorine atom, a bromine atom, an
iodine atom. Of those preferred are a fluorine atom, a chlorine atom and a bromine atom.
"Aryl" means a mono- to tri-cyclic aromatic hydrocarbon ring group having from
6 to 14 carbon atoms. Preferably, it includes phenyl, naphthyl, anthryl, phenanthryl.
More preferred are phenyl and naphthyl. "-Lower alkylene-aryl" is especially preferabl y
benzyl or phenethyl.
"Heteroaryl" means a mono- to tri-cyclic aromatic hetero ring group having from
6 to 14 carbon atoms. Preferably, it is a 5- or 6-membered monocyclic aromatic hetero
ring group; more preferably, pyridyl, pyrimidyl, pyrazyl, thienyl, furyl, oxazolyl, thiazolyl;
even more preferably pyridyl. "-Lower alkylene-heteroaryl" is especially preferably
picolyl.
"5- or 6-membered carbon ring" means a 5- or 6-membered cycloalkane or
cycloalkene, and also benzene.
"5- or 6-membered hetero ring" includes a saturated ring concretely such as
pyrrolidine, piperidine, piperazine, morpholine, and a condensed ring such as
tetrahydropyridine, furan, thiophene, pyrrole, pyridine, pyrazine, pyrimidine, oxazole,
thiazole.
"5- to 7-membered cycloalkane" includes cyclopentane, cyclohexane,
cycloheptane.
"5 to 7-membered cycloalkene" includes cyclopentene, cyclohexene,
cycloheptene.
"5- to 8-membered cyclic amine optionally having a double bond, optionally
having a bridge structure and optionally having a substituent of R7 to R11 in the ring" means
an unsaturated or saturated 5- to 8-membered cyclic amine ring having a double bond in the
ring in the former, or a bicycloamine. Preferably, it is a saturated 5- to 7-membered cyclic
amine ring, more preferably pyrrolidine, piperidine, homopiperidine, morpholine,
piperazine, even more preferably piperidine. The bicycloamine is preferably quinuclidine,
7-azabicyclo[2,2,l]heptane, 8-azabicyclo[3,2,l]octane, 9-azabicyclo[3,3,l]nonane, 3-
azabicyclo[3,2,2]nonane.
The substituent for "5- or 6-membered carbon ring or 5- or 6-membered hetero
ring optionally having a substituent" and "aryl optionally having a substituent" includes a
halogen atom, a lower alkyl, a lower alkenyl, -O-lower alkyl, -OH, -NH, -NH(lower alkyl),
-N(lower alkyl)2, -NH-CO-(lower alkyl), -N(lower alkyl)-CO-(lower alkyl), -NHCO-(0-
lower alkyl), -N(lower alkyl)-CO-(O-lower alkyl), -CN, -NO2, -CF3, -lower alkylene-OH,
-lower alkylene-halogen atom, -O-lower alkylene-OH, -lower alkylene-O-lower alkyl,
-CO-N(lower alkyl)2, -COOH, -CO-O-lower alkyl, to which, however, the present
invention should not be limited.
[0017]
The compounds of the present invention include mixtures of various isomers such
as tautomers and optical isomers, as well as individual isomers isolated from them.
The compounds of the present invention may form acid-addition salts.
Depending on the type of the substituent therein, the compounds may form salts with bases.
Concretely, the salts include acid-addition salts with a mineral acid such as hydrochloric
acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, phosphoric acid; an
organic acid such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid,
succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid,
methanesulfonic acid, ethanesulfonic acid; or an acidic amino acid such as aspartic acid,
glutamic acid; as well as salts with an inorganic base such as sodium, potassium,
masggsium, calcium, aluminium; an organic base such as methylamine, ethylamine,
ethanolamine; or a basic amino acid such as lysine, ornithine; and ammonium salts.
Further, the compounds of the present invention include hydrates,
pharmaceutically-acceptable various solvates, and crystalline polymorphic substances.
Naturally, the compounds of the present invention are not limited to those
described in the Examples given hereinunder, and include all the compounds of the above
formula (I) and their pharmaceutically-acceptable salts.
[0018]
In addition, the compounds of the present invention include prodrugs that are
metabolized in living bodies to give the compounds of the above formula (I) or their salts.
Groups to form prodrugs of the compounds of the present invention are described in, for
example, Prog. Med., 5:2157-2161 (1985) and Development of Medicines (by Hirokawa
Publishing, 1990), Vol. 7, Molecular Planning, p. 163-198.
[0019]
[Production Methods]
Taking advantage of the characteristics based on the backbone skeleton thereof or
on the type of the substituent therein, the compounds of the present invention may be
produced according to various known production methods. Depending on the type
thereof, the functional group hi the starting compounds or intermediates may be suitably
protected, or that is, may be modified into a protected group that may be readily converted
into the functional group, and this may be technically effective in producing the
compounds. After the process, the protective group may be optionally removed, and the
intended compounds may be thus obtained. The functional group includes, for example, a
hydroxyl group and a carboxyl group. Their protective groups are described, for example,
in Greene & Wuts' Protective Groups in Organic Synthesis, 2nd Ed. Depending on the
reaction condition, these may be used suitably.
Typical production methods for the compounds of the present invention are
described below.
(Production Methods)
The following schemes 1 to 6 are production methods for cyclic ketones that ar e
the starting compounds for the compounds (I) of the present invention. An indanone (6~)
that may be a starting compound for the compounds (I) of the present invention may be
produced according to the method of the following scheme 1. Specifically, an aldehyde
(1) is subjected to Knoevenagel reaction, concretely, the aldehyde (1) is reacted under he at
with a malonic acid derivative (2) in a solvent such as pyridine in the presence of a base
such as piperidine serving as a catalyst; or it is subjected to Horner-Emmons reaction,
concretely, the aldehyde (1) is reacted with a phosphonate (3) hi a solvent such as THF in
the presence of a base such as NaH, with cooling on ice or with heating. Then, the
resulting cinnamic acid derivative (4) is subjected to catalytic reduction, concretely, it is
processed with a palladium-carbon catalyst (hereinafter referred to as Pd-C) in a solvent
such as EtOH, THF or acetic acid, in a hydrogen atmosphere or in the presence of a
hydrogen source such as ammonium formate. In case where the compound has a
substituent active to Pd reduction such as a bromine group in R3 to R6 therein, a rhodiumcarbon
catalyst (hereinafter referred to as Rh-C) may be used as the catalyst. Then, the
resulting propionic acid derivative (5) is processed in the presence of an acid such as
polyphosphoric acid, methanesulfonic acid (hereinafter referred to as MsOH), MsOH-P2O5,
trifluoromethanesulfonic acid (hereinafter referred to as TfOH) or sulfuric acid, in an inert
solvent (as the case may be, the acid may serve also as a solvent), at room temperature or
under heat; or an acid chloride of the compound (5) is processed under heat in the presence
of a Lewis acid such as Aids, in a solvent such as 1,2-dichloroethane or nitromethane, or
in the absence of a solvent to give an indanone (6). (In the scheme, R13 represents a
hydrogen atom or a lower alkyl group; R14 and R15 each represent a lower alkyl group; R16
is any of R13 or R14.)
[0021]
HO.(T ,13
(2)
or
(3)
(5) (6)
(Scheme 1)
A tetralone (10) that may be a starting compound in producing the compounds (I)
of the present invention may be produced according to the method of the following scheme
2. An aldehyde (1) and a cyclopropane derivative (7) are reacted in an inert solvent such
as methylene chloride, in the presence of a Lewis acid catalyst such as TiCU with cooling
or at room temperature to give a chloride (8), and this is catalytically reduced in a hydrogen
atmosphere in the presence of a catalyst such as Pd-C, in a solvent such as EtOH, THF or
acetic acid to give a butanoic acid derivative (9). Then, (9) is cyclized in the same manner
as that for the cyclization reaction of the scheme 1 to give the tetralone (10).
(Figure Removed)
The cyclic ketone may also be produced according to the method of the following
scheme 3. Concretely, a bromide (11) is cyclized through directed lithiation with a base
such as n-BuLi, lithium or N,N-diisopropylamide (hereinafter referred to as LDA) in an
inert solvent such as THF or diethyl ether, with cooling or at room temperature.
[0023]
(Scheme 3)
Ketones (15a) and (15b) that are the starting compounds for the compounds (I) of
the present invention where R1 and R2 are both lower alkyl groups may be produced
according to the method of the folio whig scheme 4. Specifically, when R1 and R2 are the
same lower alkyl groups, then an unsubstituted ketone (13) is reacted with at least 2
equivalents of a lower alkyl halide or dialkyl sulfate, in the presence of a base such as NaH,
KN(TMS)2, t-BuOK or KOH and optionally a phase-transfer catalyst such as an ammonium
salt, in a solvent such as THF, DMF or DMSO, with cooling or under heat, when R1 and
R2 are different lower alkyl groups, then LDA is used as a base and the ketone is stepwise
alkylated to give the intended product. (In the scheme, X3 is a halogen atom.)
(Figure Removed)
A ketone (15d), which is a starting compound in producing the compounds (I) of
the present invention where R1 and R2 are both fluorine atoms, may be produced according
to the method of the following scheme 5. Specifically, a ketone (13) is reacted under heat
with an N-fluoropyridinium salt (18) in the presence of sulfuric acid and dimethyl sulfate,
in an solvent such as MeCN to give the ketone (15a). The compounds where one of R1 or
R2 is a lower alkyl group and the other is a fluorine atom may be produced by fluorinating a
monoalkyl compound (17) in the same manner as above, as in the scheme 4.
(Figure Removed)
A ketone (15f) may be produced by cyclizing a carboxylic acid derivative (19)
previously having R1 and R2, in the same manner as that for the cyclization of schemee 1 to
3, as in the scheme 6. (In the scheme, R17 represents a hydrogen atom or a bromine atom.)
[0026]
Production methods for the compounds (I) of the present invention are described
below.
Of the compounds (I) of the present invention, a compound (la) where Y1 is a
hydroxyl group may be produced by reacting a cyclic ketone derivative (15) with a
Grignard reagent or an organic lithium reagent (20) prepared from the corresponding
halide, in a solvent such as THF, diethyl ether or methylene chloride, with cooling or at
room temperature, as in the following scheme 7. (In the scheme, Z1 is a lithium atom, or a
halomagnesium.)
Of the compounds (I) of the present invention, a compound (Ib) where Y1 is a
hydroxyl group and A is N(R20)(R21) may be produced by reacting a cyclic ketone
desjjmive (15) with a nucleating reagent such as a Grignard reagent or an organic lithium
reagent having a hydroxyl group protected with a suitable protective group, and then
converting the protected hydroxyl group into an amino group, as in the following scheme 8.
Concretely, a cyclic ketone derivative is reacted with a Grignard reagent or an organic
lithium reagent (21) that has a hydroxyl group protected with a suitable protective group
such as a group of t-Bu(Me)2Si or a benzyl group, in a solvent such as THF, diethyl ether or
methylene chloride, at a temperature falling between -78°C and room temperature to give
an alcohol (22). When the protective group is a silyl group, then the product is processed
with BujNF, KF or CsF in a solvent such as THF or MeOH with cooling or under heat; and
when the protective group is a benzyl group, the product is catalytically reduced for
deprotection to give a dialcohol (23), and thereafter this is processed with MsCl or TsCl in
the presence of a base such as Et3N in a solvent such as methylene chloride to give a
sulfonyl compound (24), and then this is further reacted with an amine (25) in the presence
of a base such as (i-Pr)2EtN, Et3N or K2CO3 in a solvent such as MeCN or THF, or making
an excessive amount of the amine (25) itself serve as a base to give an amine (Ib). (In the
scheme, G is an ordinary protective group for a hydroxyl group, such as Me3Si, t-
Bu(Me)2Si, Bu3Si or benzyl; R20 and R21 are the same or different, each representing a
hydrogen atom, or an optionally-substituted lower alkyl group; regarding N(R20)R21, R20
and R21 may bond to each other to form a 5- to 8-membered cyclic amine optionally having
a substituent of R to R , ring optionally having a double bond and optionally having a
bridge structure in the ring.)
Of the compounds (I) of the present invention, a compound (Ic) where X*-A is
represented by the structural scheme mentioned below may be produced by reducing a
compound (27) produced from a ketone (15) and an amide (26), as in the scheme 9.
Concretely, a ketone (15) is reacted with an amide a-lithiate (26) prepared with LDA in a
solvent such as THF or diethyl ether, at a temperature falling between -78°C and room
temperature to give (27), and the amide bond moiety in the resulting compound is reduced
with LiAlHj or BHs in a solvent such as THF with cooling or under heat. (In the scheme,
R22 to R25 each represent a hydrogen atom or an optionally-substituted lower alkyl group;
and R to R may bond to each other to form a lower alkylene optionally having a hetero
atom in the chain thereof.)
Of the compounds (I) of the present invention, a compound (Id) where Y1 is a
hydroxyl group and X'-A is a group of the following structural formula may be produced
according to the method of the following scheme 10. Concretely, a ketone (15) is reacted
with an a-lithiate ester (28) prepared from the corresponding ester with LDA, at a
temperature falling between -78°C and room temperature to give an ester (29), then this is
processed with a reducing agent such as LiAlFLi, iBuiAlH or LiBtLt in a solvent such as
THF or MeOH with cooling on ice or at room temperature to give an alcohol (30); then in
the same manner as in the above scheme 8, the hydroxyl group in the resulting product is
converted into an amino group to give the amine (Id). (In the scheme, R26 and R27 are the
same or different, each representing a hydrogen atom or a lower alkyl group; and R26 and
R27 may bond to each other to from a lower alkylene optionally having a hetero atom in the
chain.)
[0031]
Of the compounds (I) of the present invention, a compound (le) where Y1 is a
hydroxyl group and X*-A is a group of the following structural formula may be produced
according to the method of the following scheme 11. Specifically, a ketone (15) is reacted
with a dilithio-oxime (32) prepared from an oxime and n-BuLi, in a solvent such as THF or
diethyl ether, at a temperature falling between -78°C and room temperature to give an
oxime (33); then, this is reacted with P2Os in a solvent such as chloroform or methylene
chloride with cooling, or is reacted with a sulfonylating agent such as MsCl to give a
dihydroisoxazole (34). Then, this is reacted with an alkyllithium reagent (35) in the
presence of BFaJE^O or CeCla in a solvent such as THF, methylene chloride or toluene at a
temperature falling between -78°C and room temperature to give an isoxazolidine (36); and
this is reduced with LiAlUt in THF at room temperature, or reduced in a mode of ordinary
catalytic reduction to give the amine (1 e). (In the scheme, R28 and R29 each represent a
lower alkyl group.)
(Figure Removed)
Of the compounds (I) of the present invention, a compound (If) or (Ig) where the
ring A is a piperidine ring, the ring B is a benzene ring, Y1 is a hydroxyl group, X1 is a
bond, and X2 is a methylene group, or a compound (Ih) where the ring A is a
tetrahydropyridine ring may be produced by reducing the corresponding pyridine
compound as in the following scheme 12. Concretely, a benzyl bromide (37) and an
acylpyridine (38) are reacted in the presence of a base such as LDA in a solvent such as
THF or diethyl ether with cooling or at room temperature to give a compound (39); this is
cyclized with a base such as LDA in a solvent such as THF or diethyl ether with cooling or
at room temperature, or is cyclized under heat in the presence of a base such as NaaCOa
with a Pd catalyst such as Pd(OAc)a, a ligand such s tricyclohexyl phosphine, and an
alcohol such as n-hexanol, in a solvent such as DMF to give a cyclized compound (40); and
this is reduced with Rh-C in a hydrogen atmosphere under normal pressure or increased
pressure to give a piperidine (If). (40) may be reacted with an alkyl halide in a solvent or
in the absence of a solvent at room temperature or under heat to give an ammonium salt
(41); then this is processed with a reducing agent such as NaBFLj in a solvent such as
MeOH with cooling on ice or at room temperature to give a tetrahydropyridine (Ih).
Further, (Ih) may be processed in a hydrogen atmosphere in the presence of Pd-C in a
soljpt such as EtOH at room temperature; or (41) may be subjected to direct reduction
with platinum oxide in a solvent such as EtOH in a hydrogen atmosphere at normal
pressure or increased pressure to give a piperidine (Ig).
Of the compounds (I) of the present invention, a compound (li), (Ij) or (Ik) where
the ring A is an unsubstituted piperidine ring or a tetrahydropyridine ring, X1 is a methyl ene
group optionally substituted with a lower alkyl group, and Y1 is a hydroxyl group may be
produced according to the method of the following scheme 13. Specifically, an alkylsubstituted
pyridine (42) is metallized with a base such as n-BuLi or KN(i-Pr)2; then this is
reacted with a ketone (15) in a solvent such as THF with cooling or at room temperature to
give a pyridine (43); this is reduced in various methods, for example, as in the scheme 12 to
give the piperidine (li) or (Ij) or the tetrahydropyridine (Ik). (In the scheme, R17 and R18
Jjje same or different, each representing a hydrogen atom or a lower alkyl group; and
R17 and R18 may form a lower alkylene optionally having a hetero atom in the chain
thereof.).
(Scheme 13)
Of the compounds (I) of the present invention, a compound (Im), (In), (lo) or (Ip)
where the ring B is a benzene ring, X2 is -CO-, -CH(OH)-, -CH(C1)- or -CH2-, and Y1 is a
hydroxyl group may be produced according to the method of the following scheme 14.
Specifically, a ketone (45) and a hydrazide (46) are reacted under heat in a solvent such as
EtOH, i-PrOH or acetic acid, optionally in the presence of an acid catalyst such as acetic
acid or sulfuric acid to give a hydrazide (47). This is reacted with PhI(OAc)2 or Pb(OAc)4
in an inert solvent such as 1,2-dichloroethane, THF or toluene at room temperature or under
heat to give a diketone (48), and this is then cyclized with a base such as t-BuOK, NaOEt,
DBU, KN(TMS)2 or LDA in a solvent such as THF, 1,2-dichloroethane, toluene or EtOH at
a temperature falling between -78°C and an elevated temperature to give a cyclic ketone
(Im). This is reduced with a reducing agent such as LiAltL}, NaBtLt or (i-Bu)2AJH in a
solvent such as THF, MeOH or EtOH at a temperature falling between -78 °C and room
temgerature to give an alcohol (In). (In) may be halogenated with a halogenating agent
>3»
such as SOC12 in a solvent such as MeCN with cooling or at room temperature to give a
halide (lo). (lo) may be reduced under an acidic condition with an acetic acid solvent,
using Zn (powder) under heat, or is catalytically reduced in a hydrogen atmosphere in the
presence of a catalyst such as Pd-C or Raney-Ni to give a reduced product (Ip).
Of the compounds (I) of the present invention, a compound (Iq) to (Is) where Y1
forms an oxygen-containing 5- to 7-membered ring along with R3, or any one of R1 or R2,
or the branch on -Xl-A may be produced according to the method of the following scheme
15. Specifically, a diol (49), (50) or (51) is processed in the presence of concentrated
sulfuric acid, hydrochloric acid or MsOH in a solvent such as MeOH, 1,4-dioxane or water,
at room temperature or under heat to give the intended compound. (In the scheme, X4
represents a lower alkylene, -O-lower alkylene, or -N(R30)-lower alkylene; X5 represents a
lower alkylene; Q represents a hydroxyl group-having -XJ-A as a form of-Q-OH.)
(Scheme 15)
The compounds (I) of the present invention may be subjected to substituent
modification known to anyone skilled in the art to give compounds having a desired
substituent. Typical reactions for it are described below.
Of the compounds (I) of the present invention, a compound where the substituent
R7 on the nitrogen atom of the ring A is a hydrogen atom or a lower alkyl group may be
produced by reacting a compound (I) of the present invention where R7 is a methyl group or
a benzyl group with a chloroformate in the presence of a base such as Et^N or in the
absence of a base, in a solvent such as toluene or methylene chloride at room temperature
or under heat to give a carbamate, and then processing it in the presence of a base such as
NaOH or KOH in a solvent such as water or ethanol under heat to give a compound where
js a hydrogen atom. In case where 1-chloroethyl chloroformate is used as the reactant, iipr
the resulting carbamate may be heated in methanol for deprotection. The compound
where R7 is a hydrogen atom may be reacted with an aldehyde for reductive animation ia a
solvent such as methylene chloride or 1,2-dichloroethane in the presence of an acid such as
acetic acid or a Lewis acid catalyst, using a reducing agent such as NaB(OAc)3H or
NaB(CN)H3 with cooling or at room temperature; or it is alkylated with an alky! halide in
the presence of a base such as K2CO3 in a solvent such as MeCN at room temperature or
under heat to give a compound where R7 is an alkyl group.
[0037]
Of the compounds (I) of the present invention, a compound where R3 is a cyano
group and the ring B is an aromatic ring may be produced by processing the corresponding
compound where R3 is a bromine atom with Zn(CN)2 in the presence of a catalyst such as
Pd(PPh3)4 in a solvent such as DMF or N-methylpiperidone under heat.
Of the compounds (I) of the present invention, a compound where any of R3 to R6
is an optionally-substituted aryl, lower alkenyl or lower alkynyl group may be produced
through Suzuki reaction, or that is, by reacting the corresponding compound where any of
R3 to R6 is a bromine atom or an iodine atom, with an arylboronic acid, an alkenylboronic
acid, an alkynylboronic acid or their boronate ester in the presence of a catalyst such as
Pd(PPh3)4, PdCl2(dppf) or Pd2(dba)3 along with a base such as K2CO3, Na2CO3, KOH, CsF
or NaOEt in a solvent such as DMF, N-methylpiperidone, DME or toluene or a mixed
solvent thereof with water, under heat.
Of the compounds (I) of the present invention, a compound where X1 is a
methylene group and A is NH2 may be produced by reducing the corresponding
cyanohydrin with LiAlU in a solvent such as THF. The starting compound, cyanohydrin
may be produced by reacting the corresponding ketone with (TMS)CN in the presence of
ZnI2 in a solvent such as methylene chloride or 1,2-dichloroethane under heat, or by
reacting it with KCN or NaCN under an acidic condition with acetic acid or sulfuric acid.
Of the compounds (I) of the present invention, a compound where Y1 is an azid o
group may be produced by reacting a compound (I) where Y1 is a hydroxyl group with
NaNs in the presence of an acid such as trifluoroacetic acid in a solvent such as chloroforrn,
or using the acid itself as a solvent, with cooling or under heat. This may be reduced in a
hydrogen atmosphere in the presence of Pd-C in a solvent such as EtOH, or reduced with a
reducing agent such as LiAlELj in a solvent such as THF under heat to give a compound
where Y1 is an ammo group.
Of the compounds (I) of the present invention, a compound where the ring B is an
aromatic ring and any of R3 to R6 is a nitro group may be produced by nitrating the
corresponding compound where any of R3 to R6 is a hydrogen atom under an ordinary
nitrating condition, concretely with fuming sulfuric acid in acetic anhydride with cooling,
or with concentrated nitric acid in an acetic acid solvent with cooling or at room
temperature, or with NO2BF4 in a solvent such as sulforane or THF at low temperature or
room temperature. This may be catalytically reduced with Pd-C to give the corresponding
aniline.
Of the compounds (I) of the present invention, a compound where Y1 is a lower
alkoxy group may be produced by processing the corresponding compound where Y1 is a
hydroxyl group in a lower alcohol solvent in the presence of an acid catalyst such as
camphorsulfonic acid with cooling or under heat.
[0038]
The deprotection may be attained in the presence of a suitable base in a suitable
solvent. Examples of the base are NaOH, KOH, NaOMe, NaOEt. Examples of the
solvent are ethers such as tetrahydrofuran, dioxane, diglyme; alcohols such as MeOH,
EtOH, i-PrOH; MeCN, water; and their mixtures. Depending on the type of the reaction
substrate and the reaction condition, the solvent may be suitably selected. The reaction
temperature may vary depending on the type of the starting compound and the reaction
condition, generally covering from cooling to refluxing, preferably from about 0°C to about
100°C.
The deprotection may also be attained in the presence of a metal catalyst such as
Pd-C, Pd(OH)2 or PtO2 in a suitable solvent in a hydrogen atmosphere, but may be attained
in the presence of a suitable Lewis acid in a suitable solvent. Examples of the Lewis acid
are BC13, BBr3, A1C13, and examples of the solvent are ethers such as tetrahydrofuran,
dioxane; esters such as ethyl acetate; alcohols such as MeOH, EtOH; MeCN; and their
mixtures. Depending on the type of the reaction substrate and the reaction condition, the
solvent may be suitably selected. The reaction temperature may vary depending on the
type of the starting compound and the reaction condition, generally covering from cooling
to refluxing, preferably from about -80°C to about 30°C.
Thus produced, the compounds (I) of the present invention may be isolated as
free compounds or as their pharmaceutically-acceptable salts. Salts of the compounds (I)
of the present invention may be produced by processing free bases of the compounds (I) of
the present invention for ordinary salt formation.
The compounds (I) of the present invention or their pharmaceutically-acceptable
salts may be isolated and purified as their hydrates, solvates or crystalline polymorphic
substances. The isolation and purification may be attained through ordinary chemical
treatment of extraction, concentration, evaporation, crystallization, filtration,
recrystallization, chromatography.
Various isomers may be isolated by selecting suitable starting compounds, or by
separating them based on the difference between the isomers in the physical or chemical
properties thereof. For example, optical isomers may be led into stereochemically-pure
isomers by selecting suitable starting compounds or by racemic resolution of racemic
compounds (for example, leading them into diastereomer salts with ordinary opticallyactive
acid for optical resolution).
[0039]
The NMDA receptor antagonistic activity of the compounds of the present
invention was confirmed by the following test methods.
I . J0K-801 binding test:
1) Preparation of Specimens of Rat Meninges:
The whole brain was taken out from 10-week-age SD rats (30 heads, by Nippon
SLC), and the cerebellum was removed from it. A 0.32 M sucrose solution was added to
the part containing the cerebrum, cut in a mixer, and homogenized with a Teflon
homogenizer. This was centrifuged at 2800 rpm and 4°C for 15 minutes, and the resulting
supernatant was again centrifuged at 15000 g and 4°C for 20 minutes. The pellets were
suspended in 50 mM Tris-HCL (pH 7.5) containing 0.08% Triton X-100, and kept statically
on ice for 30 minutes, then centrifuged at 15000 g and 4°C for 20 minutes. The pellets
were suspended hi 50 mM Tris-HCl (pH 7.5) added thereto, and centrifuged at 15000 g and
4°C for 20 minutes. 50 mM Tris-HCl (pH 7.5) was again added to the pellets, and
centrifuged in the same manner as before. The pellets were suspended in 20 ml of 50 mM
Tris-HCl (pH 7.5) added thereto, and homogenized with a Teflon™ homogenizer. The
membrane specimen was divided into small tubes and stored in a deep freezer (-80°C).
Before use, this was washed twice with 5 mM Tris-HCl (pH 7.5) of five times that of the
membrane specimen. Its concentration was controlled at 1 mg protein/ml with 5 mM
Tris-HCl (pH 7.5) added to it, and this was used for assay.
2) )[3H]MK-801-binding Assay:
50 ul of the rat membrane specimen (1 mg protein/ml) was added to a solution of
a test compound dissolved in 1 ul of DMSO. Then, 50 ul of a ligand solution (600 nM
glutamate, 600 nM glycine, 8 nM [3H] MK-801 (by Perkin-Elmer) was added to it and well
stirred, and reacted at room temperature for 45 minutes. Using Uni Filter Plate GF/B 96
(by Perkin-Elmer) previously coated with 0.2% polyethyleneimine, the membrane
specimen was collected, and the filter was well washed with 5 mM Tris-HCl (pH 7.5). 30
ul of Microscinti 20 (by Perkin-Elmer) was added to the filter, and the radioactivity trapped
by the filter was determined by a microplate scintillation counter (TopCount™, by
Beckman). Based on the MK-801 (final 1 uM) inhibition, 100%, of a control case of
DMSO alone, the concentration of the compound for 50% inhibition, IC50 was computed.
Th^HJMK-SOl binding affinity for the rat membrane specimen was obtained through
Scatchard analysis and Kd = 1.6 nM. The Ki value of the compound was computed
according to the calculation equation: Ki = ICso/(l + radioligand concentration (4 nM) in
assay)/Kd value (1.6 nM)).
As a result, the compounds of the present invention exhibited good NMD A
receptor affinity. The Ki value of the NMD A receptor affinity of some typical compounds
of the present invention is shown in Table 1 below.
(Table Removed)
2. Intracellular Calcium Concentration Determination Test by FLIPR (Fluorometric
Imaging Plate Reader):
1) Preparation of Rat First-Generation Neurocytes:
Anesthetized with ether, Wistar rats (by Nippon SLC) of pregnancy 19 days was
let die from loss of blood by breast incision. The abdomen was cut open, and the womb
was taken out, and the fetus was taken out of it. The whole brain was taken out, then the
hemicerebrum was isolated in Neurobasal medium (Glu, Asp-free) (by Gibco), and the
meninx was removed. The hemicerebrum was recovered by centrifugation, and
suspended in a cell-dispersing solution (0.36 mg/ml papain, 150U/ml DNase I, 0.02% Lcysteine
monohydrochloride monohydrate, 0.02% bovine serum albumin, 0.5% glucose,
Ca2+ Mg2+-free PBS), and processed at 37°C for 15 minutes. This was centrifuged at 400
PuJgr 5 minutes, and the supernatant was removed by suction. This was suspended in a
neurocyte culture medium (by Sumitomo Bakelite), and the cell masses were removed by
filtration. The number of the living cells was counted, and 100,000 cells/well were
incubated on a 96-well plate (Biocoat PDL96W black/clear, by Nippon Becton Dickinson)
at 37°C in 5% CO2.
[0042]
2) Intracellular Calcium Concentration Determination by FLIPR (Fluorometric Imaging
Plate Reader):
The culture of rat first-generation neurocytes (DIV7-9) was removed by suction,
and the cells were washed once with an assay buffer (Hank's Balanced Salt Solution (Ca2+,
Mg2+-free), 20 mM Hepes-NaOH (pH 7.4), 1 mM CaCl2). 100 ul of the assay buffer
containing FluoS (by Dojin Chemical) was added thereto, and incubated for 1 hour (37°C,
5% CO2). The cells were washed three times with 100 ul of the assay buffer, and then a
test compound solution dissolved in 1 ul of DMSO, and 100 fil of the assay buffer
containing 2.5 uM (final concentration) tetrodotoxin were added to it and incubated for 30
minutes (37°C, 5% CO2). The fluorescent intensity was measured at intervals of 2
seconds. Ten seconds after the measurement start, 50 ul of a ligand solution (Hank's
Balanced Salt Solution (Ca2+, Mg2+-free), 20 mM Hepes-NaOH (pH 7.4), 1 mM CaCl2, 9
uM NMDA, 30 uM glycine) containing the test compound solution dissolved in 0.5 ul of
DMSO was added to it, and the fluorescent intensity of the system was measured for 120
seconds from the start of the measurement. The data measured for 120 seconds (60 times
in total) were averaged. Based on the 10 uM MK-801 inhibition, 100%, of a control case
of DMSO alone, the concentration of the compound for 50% inhibition, ICso was
computed.
A pharmaceutical composition comprising the compound of the present
invention, in combination with a pharmaceutically acceptable carrier is found to show
suiprising properties. The pharmaceutical composition of the present invention is
therefore synergistic.
As a result, the compounds of the present invention exhibited good NMDA
receptor antoginizing effect.
The pharmaceutic composition that contains, as the active ingredient thereof,
one or more of the compouni s of the present invention and their pharmaceuticallyacceptable
salts may be form ilated, optionally along with carriers and vehicles for ordinary
pharmaceutical application a Ld other additives, as tablets, powders, infinitesimal grains,
granules, capsules, pills, liqu ds, injections, suppositories, ointments, fomentations, and is
administered to patients oral] f or non-orally.
The clinical dose to human of the compound of the present invention may be
suitably determined, depend] ig on the condition, the body weight, the age and the sex of
the patient to whom the com] ound is applied, hi general, it may be from 0.1 to 500
mg/adult/day for oral administration, and from 0.01 to 100 mg/adult/day for non-oral
administration, and this may be administered all at once or in several times. The dose may
vary under various conditions, and as the case may be, it may be smaller than the abovementioned
dose range.
The solid composition for oral administration of the compound of the present
invention may be tablets, powders or granules. In the solid composition, one or more
active substances may be mixed with at least one inert diluent, such as lactose, mannitol,
glucose, hydroxypropyl cellulose, microcrystalline cellulose, starch, polyvinylpyrrolidone,
magnesium metasilicate aluminate. According to an ordinary manner, the composition
may contain any other additive than such an inert diluent, for example, lubricant such as
magnesium silicate, disintegrator such as calcium cellulose glycolate, stabilizer such as
lactose, solubilizer or dissolution promoter such as glutamic acid, aspartic acid. The
tablets and pills may be coated with sugar or with gastric-coating or enteric-coating film.
[0044]
The liquid composition for oral administration includes pharmaceuticallyacceptable
emulsion, solution, suspension, syrup and elixir, and contains an ordinary inert
diluent such as pure water, ethyl alcohol. The composition may contain any other additive
than such an inert diluent, for example, auxiliary agent such as solubilizer, dissolution
wetting agent, suspending agent, as well as sweetener, flavoring, fragrance, and
preservative. The injection for non-oral administration includes germ-free water-base or
waterless solution, suspension and emulsion. The diluent for water-base solution and
suspension include, for example, distilled water for injection and physiological saline
water. The diluent for the waterless solution and suspension includes, for example,
propylene glycol, polyethylene glycol, vegetable oil such as olive oil, alcohols such as ethyl
alcohols, Polysorbate 80 (trade name).
The composition may further contain any other additive such as isotonizer,
preservative, wetting agent, emulsifier, dispersant, stabilizer, solubilizer, dissolution
promoter. These may be sterilized by filtration through a bacteria-trapping filter, or by
addition of germicide, or through irradiation with light. As the case may be, a germ-free
solid composition may be prepared, and it may be dissolved in germ-free water or germfree
solvent for injection to give the intended liquid composition before use.
EXAMPLES
[0045]
The compounds of the present invention are described with reference to the
following Examples. The starting compounds for the compounds of the present invention
include new compounds, and their production is illustrated as Reference Examples
hereinunder.
Reference Example 1:
3-(3-Bromo-4-fluorophenyl)propionicacid:
Piperidine (1 ml) was added to a pyridine (250 ml) solution of 3-bromo-4-
fluorobenzaldehyde (20 g) and malonic acid (51 g), followed by heating under reflux for
hours. After completion of the reaction, the solvent was evaporated under reduced
pressure, water was added, and this was neutralized with 1 N hydrochloric acid added
thereto with stirring. The precipitated matter was collected by filtration, and the resulting
(2E)-3-(3-bromo-4-fluorophenyl)acrylic acid was dissolved in THF (200 ml), followed by
slitting with 5% Rh-C (3 g) in a hydrogen atmosphere at room temperature for 12 hours.
The insoluble matter was removed by filtration, and the solvent was evaporated under
reduced pressure to obtain the compound (15 g) of Reference Example 1.
In Reference Example 2, the compound shown in Table 2 was produced in the
same manner as in Reference Example 1.
Reference Example 3:
3-(2-Fluoro-5-methylphenyl)propionicacid:
Piperidine (0.3 ml) was added to a pyridine (50 ml) solution of 2-fluoro-5-
methylbenzaldehyde (4.2 g) and malonic acid (16 g), followed by heating under reflux for 3
hours. After completion of the reaction, the solvent was evaporated under reduced
pressure, water was added, and this was neutralized with 1 N hydrochloric acid added
thereto with stirring. The precipitated matter was collected by filtration, and the resulting
(2E)-3-(2-fluoro-5-methylphenyl)acrylic acid was dissolved in a mixed solvent (70 ml) of
THF and EtOH, followed by stirring with 10% Pd-C (0.5 g) in a hydrogen atmosphere at
room temperature for 12 hours. The insoluble matter was removed by filtration, and the
solvent was evaporated under reduced pressure to obtain the compound (5.1 g) of
Reference Example 3.
In Reference Examples 4 to 7, the compounds shown in Table 2 were produced in
the same manner as in Reference Example 3.
[0046]
Reference Example 8:
3-(4-Bromo-2-fluoro-5-methylphenyl)propionicacid:
The compound (3.0 g) of Reference Example 3 was dissolved in a mixed solvent
of trifluoroacetic acid (15 ml) and concentrated sulfuric acid (3 ml), and at room
temperature, N-bromosuccinimide (hereinafter referred to as NBS) (3.5 g) was added
thereto gradually, followed by stirring at that temperature for 1 hour. The reaction
solution was poured into ice-water, followed by extraction with chloroform and drying over
anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain
the compound (3.7 g) of Reference Example 8.
In Reference Examples 9 to 12, the compounds shown in Table 2 were produced
in the same manner as in Reference Example 8.
Reference Example 13:
Methyl 3-(3,4,5-trifluorophenyl)-2,2-dimethylpropionate:
At -20°C, a 1.6 M n-BuLi/hexane solution (100 ml) was added to a THF (200 ml)
solution of i-PrjNH (25 ml), followed by stirring at that temperature for 30 minutes. This
was cooled to -78°C, then methyl 3-(3,4,5-trifluorophenyl)propionate (24 g) was added
thereto, followed by further stirring for 1 hour. Then, Mel (10 ml) was added, followed
by further stirring for 1 hour. The reaction solution was heated to 0°C, then an aqueous
saturated ammonium chloride solution was added, followed by extraction with diethyl
ether, and then washing with 1 N hydrochloric acid, an aqueous saturated sodium
hydrogencarbonate solution, water and saturated brine. After drying over anhydrous
sodium sulfate, the solvent was evaporated under reduced pressure to obtain methyl 3-
(3,4,5-trifluorophenyl)-2-methylpropionate.
Next, at -78°C, methyl 3-(3,4,5-trifluorophenyl)-2-methylpropionate produced hi
the above was added to LAD that had been prepared similarly from i-PraNH (25 ml),
followed by stirring at that temperature for 1 hour. Then, Mel (10 ml) was added,
followed by furtherstirring for 1 hour. The reaction solution was heated to 0°C, an
aqueous saturated ammonium chloride solution was added, followed by extraction with
diethyl ether. This was washed with 1 N hydrochloric acid, an aqueous saturated sodium
hydrogencarbonate solution, water and saturated brine, then dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure to obtain the compound (21
g) of Reference Example 13.
Reference Example 14:
6,7-Dichloroindan-1 -one:
3-(3,4-Dichlorophenyl)propionic acid (500 mg) was stirred in TfOH (1.5 ml) in
an argon atmosphere at 100°C for 24 hours. The reaction solution was poured into icewater,
extracted with diethyl ether, washed with water, an aqueous saturated sodium
hydrogencarbonate solution and saturated brine, then dried over anhydrous sodium sulfate.
Then, the solvent was evaporated under reduced pressure. The residue was purified by
silica gel column chromatography (eluent: n-hexane/ethyl acetate = 5/1) to obtain 5,6-
dichloroindan-1-one (115 mg) and the compound (44 mg) of Reference Example 14.
In Reference Examples 15 to 22, the compounds shown in Tables 2 and 3 were
produced in the same manner as in Reference Example 14.
Reference Example 23:
4-Bromo-6-fluoro-7-methoxy-l -indanone:
The compound (20 g) of Reference Example 9 was dissolved in TfOH (200 ml),
followed by stirring in an argon atmosphere at 50°C for 2 hours. The reaction solution
was poured into ice-water, and with stirring and cooling on ice, this was neutralized with an
aqueous saturated ammonia. The precipitated matter was collected by filtration, washed
with water, and dried under reduced pressure to obtain the compound (13 g) of Reference
Example 23 as a brown solid.
hi Reference Examples 24 to 25, the compounds shown hi Tables 2 and 3 were
produced in the same manner as in Reference Example 14.
In Reference Example 26, the compound shown hi Table 3 was obtained from the
compound obtained in Reference Example 13 and shown in Table 2, in the same manner as
in Reference Example 14.
Reference Example 27:
6-Fluoro-2,2-dimethylindan-1 -one:
Mel (0.354 ml) and 55% oily NaH (248 mg) were added to a THF (10 ml)
solution of 6-fluoroindan-l-one (388 mg) in an argon atmosphere at room temperature,
followed by stirring at that temperature for 30 minutes. An aqueous saturated ammonium
chloride solution was added to the reaction liquid, followed by extraction with diethyl
ether, washing with saturated brine, then drying over anhydrous sodium sulfate. Then, the
solvent was evaporated under reduced pressure. The residue was purified by silica gel
column chromatography (eluent: n-hexane/ethyl acetate =10/1) to obtain the compound
(241 mg) of Reference Example 27.
In Reference Examples 28 to 55, the compounds shown in Tables 3 to 5 were
produced in the same manner as in Reference Example 27.
[0049]
Reference Example 56 and Reference Example 57:
7-Chloro-6-fluoro-2,2-dimethyUndan-l-one, and 5-Chloro-6-fluoro-2^-dimethylindan-lone:
3-(3-Chloro-4-fluorophenyl)propionic acid (9.8 g) was dissolved in TfOH (40
ml), followed by stirring in an argon atmosphere at 100°C for 24 hours. The reaction
solution was poured into ice-water, extracted with diethyl ether, and washed with saturated
sodium hydrogencarbonate, and saturated brine. Then, the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column chromatography (eluent:
n-hexane/ethyl acetate = 10/1 to 3/1) to obtain a mixture (7.2 g) of 5-chloro-6-fluoroindan-
1-one and 7-chloro-6-fluoroindan-l-one. Then, this was dissolved in THF (200 ml), Mel
(6.1 ml) was added thereto, and with stirring at room temperature, 55% oily NaH (4.3 g)
was added thereto gradually with taking 30 minutes. After the heat generation stopped, an
aqueous saturated ammonium chloride solution was added to the reaction solution,
followed by extraction with diethyl ether, and washing with saturated brine. This was
driwFover anhydrous magnesium sulfate, the solvent was evaporated under reduced
pressure, and the residue was purified by silica gel column chromatography (eluent: nhexane/
ethyl acetate = 30/1 to 10/1) to obtain the compound (0.85 g) of Reference Example
56 and the compound (5.9 g) of Reference Example 57.
In Reference Examples 58 to 61, the compounds shown in Table 5 were produced
in the same manner as in Reference Examples 56 and 57.
Reference Example 62:
4,6,7-Tribromo-2,2-dimethylindan-1 -one:
6-Bromo-2,2-dimethylindan-l-one (600 mg) was dissolved in a mixed solution of
trifluoroacetic acid (5 ml) and concentrated sulfuric acid (4 ml), and at room temperature,
NBS (1.34 g) was added thereto, followed by stirring at that temperature for 3 hours. The
reaction solution was poured into ice-water and neutralized with an aqueous saturated
ammonia. The precipitated matter was collected by filtration to obtain the compound (1.1
g) of Reference Example 62.
In Reference Example 63, the compound shown in Table 5 was produced in the
same manner as in Reference Example 62.
[0050]
Reference Example 64:
6-Fluoro-7-methoxy-2,2-dimethylindan-l-one:
i-Pr2NEt (8.9 ml) and 10% Pd-C (1 g) were added to an EtOH (300 ml) solution
of the compound (15 g) of Reference Example 53, followed by stirring in a hydrogen
atmosphere at room temperature for 1 hour. The insoluble matter was removed by
filtration, the solvent was evaporated under reduced pressure, and water was added to the
residue, followed by extraction with diethyl ether and washing with saturated brine. This
was dried over anhydrous magnesium sulfate, and the solvent was evaporated under
reduced pressure to obtain the compound (1.1 g) of Reference Example 64.
In Reference Examples 65 and 66, the compounds shown in Table 6 were
produced in the same manner as in Reference Example 64.
ReHrence Example 67:
7-Fluoro-3,3-dimethylquinoline-2,4(lH,3H)-dione:
P2O5 (10 g) was added to MsOH (100 ml), followed by stirring at 80°C for 30
minutes. 3-[(3-Fluorophenyl)amino]-2,2-dimethyl-3-oxopropionic acid (8 g) was added,
followed by stirring at that temperature for 2 hours. The reaction solution was cooled to
room temperature, poured into ice-water, and with stirring, an aqueous saturated ammonia
was added thereto thereby making it basic. The precipitated matter was collected by
filtration, washed with water, and dried under reduced pressure to obtain the compound (6
g) of Reference Example 67.
Reference Example 68:
Ethyl 4-(l-hydroxy-2,2,6-trimethyl-2,3-dihydro-lH-inden-l-yl)piperidin-l-carboxylate:
Et3N (7 ml) and ethyl chloroformate (4 ml) were added to a toluene (50 ml)
solution of a desalted product (1.5 g) of the compound of Example 6, followed by stirring at
100°C for 2 hours. The reaction solution was subjected to liquid-liquid separation with
ethyl acetate/water, and the organic layer was washed with saturated brine, then dried over
anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The
residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate
5/1) to obtain the compound (1.04 g) of Reference Example 68.
In Reference Examples 69 and 70, the compounds shown in Table 6 were
produced in the same manner as in Reference Example 68. hi Reference Example 71, the
compound shown in Table 6 was produced in the same manner as in Reference Example
27. In Reference Example 72, the compound shown in Table 7 was produced in the same
manner as in Reference Example 68.
[0051]
Reference Example 73:
4-(2-Fluoro-5 -methoxy)butanoic acid:
At room temperature, 2-fluoro-5-methoxybenzaldehyde (2.5 g) was added to a
1,2-dichloroethane (50 ml) solution of T1CL4 (2.06 ml), followed by stirring at that
teiiperature for 30 minutes. This was cooled to -78°C, then 1-ethoxy-l-
[(trimethylsilyl)oxy]cyclopropane (3.76 ml) was added thereto, and with stirring, this was
heated to 0°C, taking 3.5 hours. The reaction solution was poured into ice-water,
extracted with chloroform, washed with saturated brine, then dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The resulting yellow oil
was dissolved in ethanol (100 ml), and 10% Pd-C (450 mg) was added thereto, followed by
stirring in a hydrogen atmosphere under normal pressure for 2 hours. The insoluble
matter was removed by filtration using Celite, and the solvent was evaporated under
reduced pressure to obtain an yellow oil. Then, this was dissolved in EtOH (50 ml), and
an aqueous 1 N NaOH solution (17.5 ml) was added thereto, followed by stirring at room
temperature for 4 days. The reaction solution was made acidic with diluted hydrochloric
acid, then extracted with ethyl acetate, and washed with saturated brine. This was dried
over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to
obtain the compound (3.45 g) of Reference Example 73 as a brown solid.
In Reference Example 74, in the same manner as in Reference Example 23; in
Reference Example 75, in the same manner as in Reference Example 27; in Reference
Example 76, in the same manner as in Reference Example 3; in Reference Example 77, in
the same manner as in Reference Example 14; in Reference Example 78, in the same
manner as in Reference Example 27; in Reference Example 79, in the same manner as in
Reference Example 23; in Reference Example 80, in the same manner as in Reference
Example 27; in Reference Example 81, in the same manner as in Reference Example 117;
the compounds shown in Table 7 were produced.
Reference Example 82:
6-Bromo-2,2-dimethyl-7-methoxyindan-1 -one:
At room temperature, 55% oily NaH (760 mg) was added to a THF solution of
the compound (989 mg) of Reference Example 81 and Mel (1.09 ml), followed by stirring
at 60°C for 3 hours. An aqueous saturated ammonium chloride solution was added,
followed by liquid-liquid separation with a mixed solvent (3/1) of ethyl acetate and THF.
ThlFbrganic layer was washed with saturated brine, dried with sodium sulfate, and the
solvent was evaporated under reduced pressure. The residue was purified by silica gel
chromatography (eluent; hexane/ethyl acetate = 6/1) to obtain 6-bromo-2,2-dimethyl-7-
hydroxyindan-1-one (1.1 g). Then, Mel (0.298 ml) and K2CO3 (1.81 g) were added to its
DMF solution in that order, followed by stirring at 60°C for 24 hours. After completion of
the reaction, water was added, followed by liquid-liquid separation with ethyl acetate.
The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate,
and the solvent was evaporated under reduced pressure. The residue was purified by silica
gel column chromatography (eluent: hexane/ethyl acetate = 9/1 to 4/1) to obtain the
compound (644 mg) of Reference Example 82 as a colorless powdery solid.
Reference Example 83:
6-Fluoro-7-hydroxy-2,2-dimethylindan-l-one:
With cooling on ice, 1 M BBr3/methylene chloride solution (60 ml) was gradually
dropwise added to a methylene chloride solution of the compound (8.10 g) of Reference
Example 64. This was stirred overnight at room temperature, and an aqueous saturated
sodium hydrogencarbonate solution was added thereto, followed by extraction with
methylene chloride. This was washed with saturated brine, dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure to obtain the compound
(7.86 g) of Reference Example 83 as a brown solid.
[0052]
Reference Example 84:
7-Ethoxy-6-fluoro-2,2-dimethylindan-l-one:
At room temperature, EtI (5.0 ml) was added to a DMF solution of the compound
(4.0 g) of Reference Example 83 and KaCOs (8.54 g), followed by stirring overnight at that
temperature. Water was added to the reaction solution, followed by extraction with ethyl
acetate and washing with water and saturated brine. This was dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced pressure to obtain the
compound (4.47 g) of Reference Example 84 as a brown oil.
In Reference Example 83, in the same manner as in Reference Example 3; in
Reference Example 86, in the same manner as in Reference Example 96; in Reference
Example 87, in the same manner as in Reference Example 23 and then in the same manner
as in Reference Example 27; hi Reference Example 88, in the same manner as hi Reference
Example 3; in Reference Example 89, in the same manner as in Reference Example 67; in
Reference Example 90, in the same manner as in Reference Example 27; in Reference
Example 91, hi the same manner as hi Reference Example 3; the compounds shown in
Tables 7 and 8 were produced.
Reference Example 92:
4-Fluoro-6-hydroxy-2,2,7-trimethylhidan-1 -one:
In the same manner as in Reference Example 14, the compound (442 mg) of
Reference Example 92, and a mixture (239 mg) of 4-fluoro-6-hydroxy-2,2,5-
trimethylindan-1-one and 4-fluoro-6-hydroxy-2,2-dimemylindan-l-one were obtained each
as a brown solid, from the compound of Reference Example 91.
In Reference Example 93, the compound shown in Table 8 was produced from
the compound of Reference Example 92, in the same manner as in Reference Example 27.
Reference Example 94:
1 -(4-Fluoro-2-hydroxyphenyl)-2-methylpropan-1 -one:
A mixture of A1C13 (150 g) and NaCl (150 g) was melted at 160°C with stirring.
At the same temperature, 3-fluorophenyl 2-methylpropanoate (50 g) was added, followed
by stirring for 1 hour. The reaction liquid was cooled, then with cooling on ice, water was
gradually added thereto to break AlCh. Then, concentrated hydrochloric acid was added,
followed by heating and stirring so as to dissolve the mass. When the mass became
suspended, this was cooled, and extracted with diethyl ether, washed with saturated brine,
dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure
to obtain the compound (49 g) of Reference Example 94 as a brown oil.
Reference Example 95:
l-(3,5-Dibromo-4-fluoro-2-hydroxyphenyl)-2-methylpropan-l-one:
At -10°C, NBS (1 15 g) was added to a mixed solution of the compound (49 g) of
Reference Example 94 in trifluoroacetic acid (200 ml) and concentrated sulfuric acid (40
ml), taking 1 hour. Then, this was stirred at -10°C to 0°C for 1 hour, and the reaction
solution was poured into ice-water, followed by extraction with diethyl ether. The organic
layer was concentrated under reduced pressure, the residue was subjected to liquid-liquid
separation with an aqueous saturated sodium hydrogencarbonate solution and diethyl ether,
and the organic layer was washed several times with an aqueous 5% sodium thiosulfate
solution. This was further washed with saturated brine, dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure to obtain a brown oil.
After allowing it as it is, partial crystallization was found. The crystallized part was
collected by filtration to obtain the compound (91 g) of Reference Example 95 as a brown
crystal.
Reference Example 96:
N'-[l-(3,5-dibromo-4-fluoro-2-hydroxyphenyl)-2-methylpropylidene]-l-methylpiperidine-
4-carbohydrazide acetate:
Acetic acid (7.3 ml) was added to an i-PrOH solution of the compound (34 g) of
Reference Example 95 and l-methylpiperidine-4-carbohydrazide (20 g), followed by
heating under reflux for 5 hours. Since an insoluble matter precipiated therein, the
reaction solution was cooled to room temperature, and it was collected by filtration and
washed with i-PrOH to obtain the compound (40 g) of Reference Example 96 as a crystal.
Reference Example 97:
3,4-Difluoro-5-methoxybenzaldehyde:
1 .58 M n-BuLi/hexane solution (1 .4 ml) was added to a diethyl ether solution of
5-bromo-l,2-difluoro-3-methoxybenzene (497 nig) in an argon atmosphere at -70°C,
followed by stirring at that temperature for 1 hour. DMF (0.259 ml) was added, followed
byjpring for 30 minutes. After completion of the reaction, water was added, followed by
extraction with diethyl ether, washing with saturated brine, and drying over anhydrous
sodium sulfate. The solvent was evaporated under reduced pressure to obtain the
compound (317 mg) of Reference Example 97.
In Reference Example 98, the compound in Table 8 was produced in the same
manner as in Reference Example 84.
Reference Example 99:
1 -(2-Fluoro-6-methoxyphenyl)-2-methylpropan-1 -ol:
1.58 M n-BuLi/hexane solution (152 ml) was gradually added to a THF solution
of 3-fluoroanisole (28 g) andN,N,N',N',N"-pentamethyldiethylenetriamine (48 ml), in an
argon atmosphere at -78°C, followed by stirring at that temperature for 1 hour.
Isobutylaldehyde (22 ml) was gradually added to it, and further stirred for 15 minutes.
This was gradually heated to room temperature, then water was added to it, and extracted
with diisopropyl ether. This was washed with water and saturated brine, dried over
anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain
the compound (47 g) of Reference Example 99 as an oil.
In Reference Example 100, in the same manner as in Reference Example 27; in
Reference Example 101, in the same manner as in Reference Example 1; in Reference
Example 102, in the same manner as in Reference Example 23; in Reference Example 103,
in the same manner as in Reference Example 27; in Reference Example 104, in the same
manner as in Reference Example 3; the compounds shown in Table 9 were produced.
[0054]
Reference Example 105:
4-Bromo-5,5-difluoro-7-methoxyindan-l-one:
A trifluoroacetic acid/concentrated sulfuric acid (5/1) mixed solution of the
compound (4.4 g) of Reference Example 104 was cooled to 0°C, and NBS (3.8 g) was, as
divided into 10 portions, separately added thereto, followed by stirring at 0°C for 1 hour.
Water was added to the reaction solution, followed by extraction with ethyl acetate,
wasTing with saturated brine, and drying over anhydrous sodium sulfate. The solvent was
evaporated under reduced pressure to obtain 3-(2-bromo-3,4-difluoro-5-
methoxyphenyl)propionic acid as a crude product. Then, this was dissolved in TfOH (8.8
ml), followed by stirring at room temperature for 30 minutes. The reaction solution was
poured into ice-water, followed by extraction with ethyl acetate, washing with saturated
brine, and drying over anhydrous sodium sulfate. The solvent was evaporated under
reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: n-hexane/ethyl acetate = 4/1) to obtain the compound (2.84 g) of Reference
Example 105.
Reference Example 106:
5,5-Difluoro-7-methoxy-2,2-dimethylindan-l-one:
At room temperature, 55% oily NaH (978 mg) was added to a THF solution of
the compound (2.8 g) of Reference Example 105 and Mel (1.4 ml), followed by stirring at
that temperature for 1 hour. An aqueous saturated ammonium chloride solution was
added, followed by extraction with ethyl acetate, washing with saturated brine, and drying
over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to
obtain 4-bromo-5,5-difluoro-7-methoxy-2,2-dimethylindan-l-one as a crude product.
Then, this was dissolved in EtOH, 10% Pd-C was added, followed by stirring in a hydrogen
atmosphere (1 atmospheric pressure) at room temperature for 20 hours. The insoluble
matter was removed by filtration using Celite, the solvent was evaporated under reduced
pressure, and the residue was purified by silica gel column chromatography (eluent: nhexane/
ethyl acetate = 9/1) to obtain the compound (550 mg) of Reference Example 106 as
a colorless oil.
Reference Example 107:
5,6-Difluoroindan-1 -ol:
With cooling on ice, NaBtL1 (774 mg) was added to an MeOH solution of 5,6-
difluoroindan-1-one (3.44 g), followed by stirring at that temperature for 1 hour. Acetone
was added to the reaction solution, then the solvent was evaporated under reduced pressure,
ami-Hie residue was subjected to liquid-liquid separation with saturated ammonium chloride
and ethyl acetate. The organic layer was washed with saturated brine, dried over
anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain
the compound (4.29 g) of Reference Example 107 as an oil.
[0055]
Reference Example 108:
5,6-Difluoro-1 - {[2-(trimethylsilyl)ethoxy]methoxy} indane:
With cooling on ice, 55% oily NaH (1.31 g) and l-(chloromethoxy)-2-
(trimethylsilyl)ethane (5.0 g) were added to a DMF solution of the compound (4.29 g) of
Reference Example 107, followed by stirring overnight at room temperature. Water was
added to the reaction solution, extracted with ethyl acetate, washed with water and
saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column chromatography (eluent:
n-hexane/ethyl acetate = 20/1) to obtain the compound (4.25 g) of Reference Example 108
as an oil.
Reference Example 110:
5,6-Difluoro-7-hydroxymethyl-l-{[2-(trimethylsilyl)ethoxy]methoxy}indane:
1.58 M n-BuLi/hexane solution (3.6 ml) was added to a THF solution of the
compound (1.46 g) of Reference Example 107 in an argon atmosphere at -78 °C, followed
by stirring at that temperature for 1 hour. DMF (0.49 ml) was added to it at that
temperature, and gradually heated to room temperature, and then subjected to liquid-liquid
separation with an aqueous saturated ammonium chloride solution and ethyl acetate, and
the organic layer was washed with saturated brine. This was dried over anhydrous sodium
sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by
silica gel column chromatography (eluent: n-hexane/ethyl acetate = 4/1) to obtain 5,6-
difluoro-7-formyl-l-{[2-(trimethylsilyl)ethoxy]methoxy}indane (1.31 g) as an oil. With
cooling on ice, NaBtLj (227 mg) was added to its MeOH solution, followed by stirring at
that temperature for 1 hour. Acetone was added to the reaction solution, then the solvent
wawevaporated under reduced pressure, and the residue was subjected to liquid-liquid
separation with saturated ammonium chloride and ethyl acetate. The organic layer was
washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure to obtain the compound (929 mg) of Reference Example
110 as an oil.
Reference Example 111:
5,6-Difluoro-7-methoxymethyl-l-{[2-(trimethylsilyl)ethoxy]methoxy}indane:
With cooling on ice, 55% oily NaH (147 mg) was added to a THF solution of the
compound (929 mg) of Reference Example 110 and Mel (0.21 ml), followed by stirring
overnight at room temperature. The reaction solution was subjected to liquid-liquid
separation with an aqueous saturated ammonium chloride solution and ethyl acetate, and
the organic layer was washed with saturated brine. This was dried over anhydrous sodium
sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by
silica gel column chromatography (eluent: n-hexane/ethyl acetate = 20/1) to obtain the
compound (905 mg) of Reference Example 111 as an oil.
[0056]
Reference Example 112:
5,6-Difluoro-7-methoxymethylindan-1 -ol:
CsF (1.59 g) was added to a DMF solution of the compound (899 mg) of
Reference Example 111, followed by stirring overnight under heat at 130°C. The reaction
solution was cooled to room temperature, ethyl acetate was added thereto and stirred, and
the insoluble matter was removed by filtration using Celite. The filtrate was concentrated
under reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: n-hexane/ethyl acetate = 2/1) to obtain the compound (479 mg) of Reference
Example 112 as an oil.
Reference Example 113:
5,6-Difluoro-7-methoxymethylindan-1 -one:
The compound (479 mg) of Reference Example 112, N-methylmorpholine (393
mg) and Pr4N+RuO4" (79 mg) were added to a 1/1 mixed solvent of MeCN and methylene
chloride, followed by stirring overnight at room temperature. The solvent was evaporated
under reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: n-hexane/ethyl acetate = 2/1) to obtain the compound (450 mg) of Reference
Example 113 as an oil.
In Reference Example 114, in the same manner as in Reference Example 27; in
Reference Example 115, in the same manner as in Reference Example 8 but from the
compound of Reference Example 71; the compounds shown in Table 9 were produced.
Reference Example 116:
1 -(2-Fluoro-6-hydroxyphenyl)-2-methylpropan-1 -one:
A methylene chloride solution of the compound (43 g) of Reference Example 99
was added to 1 M BBrs/methylene chloride solution (250 ml) in an argon atmosphere at -
78°C, stirred for 1 hour at a temperature falling between that temperature and -40°C, then
gradually heated to 0°C. Water was added to it for liquid-liquid separation, and the
organic layer was washed with saturated brine. This was dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure to obtain the compound (38
g) of Reference Example 116 as an oil.
[0057]
Reference Example 117:
1 -(3-Bromo-6-fluoro-2-hydroxyphenyl)-2-methylpropan-l -one:
Bromine (60 g) was gradually drop wise added to a toluene solution of t-BuNHa
(51 g) in an argon atmosphere at -30°C. This was stirred fro 30 minutes at that
temperature, then cooled to -78°C, and a methylene chloride solution of the compound (70
g) of Reference Example 116 was gradually added to it. This was further stirred for 1
hour at that temperature, then gradually heated to 0°C, taking 4 hours. Water was added
to tne reaction solution, extracted with ethyl acetate, washed with water and saturated brine,
then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure to obtain the compound (88 g) of Reference Example 117 as an oil.
Reference Example 118:
N'-[l-(3-bromo-6-fluoro-2-hydroxyphenyl)-2-methylpropylidene]quinuclidine-3-
carbohydrazide:
A mixture of methyl quinuclidine-3-carboxylate hydrochloride (1.0 g) and
hydrazine monohydrate (3.0 ml) was stirred for 2 hours under heat at 100°C. Still under
heat, this was concentrated under reduced pressure, and the residue was dissolved in i-
PrOH. To it were added the compound (2.7 g) of Reference Example 117 and acetic acid
(0.596 ml), followed by heating under reflux for 7 hours. After completion of the
reaction, the solvent was evaporated under reduced pressure, and the residue was subjected
to liquid-liquid separation with 0.5 N hydrochloric acid and diisopropyl ether. The
aqueous layer was again washed with diisopropyl ether, then neutralized with sodium
hydrogencarbonate, and extracted three times with chloroform. The chloroform layer was
dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure to obtain the compound (710 mg) of Reference Example 118 as a colorless
amorphous substance.
Reference Example 119:
1 -(2-Fluoro-6-methoxyphenyl)-2-methylpropan-1 -one:
With cooling on ice, SOa-pyridine (139 g) was gradually added to a DMSO
solution of the compound (47 g) of Reference Example 99 and EtaN (152 ml), followed by
stirring overnight at room temperature. Water was added to the reaction solution,
extracted with diisopropyl ether, washed with diluted hydrochloric acid, water and
saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure to obtain the compound (43 g) of Reference Example 119 as an oil.
Refwence Example 120:
6-Fluoro-7-methoxy-2,2-dimethyl-1 -trimethylsiloxayindane-1 -carbonitrile:
At room temperature, (TMS)CN (930 mg) was added to a 1,2-dichloroethane
solution of the compound (485 mg) of Reference Example 64 and ZnI2 (37 mg), followed
by stirring at that temperature for 2 hours. An aqueous saturated sodium
hydrogencarbonate solution was added to the reaction solution, extracted with chloroform,
washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure to obtain the compound (710 mg) of Reference Example
120.
[0058]
Reference Example 121:
Methyl (6-fluoro-l-hydroxy-7-methoxy-2^-dimethyl-2,3-dihydro-lH-uidene)acetate:
2.67 M n-BuLi/hexane solution (17 ml) was added to a THF solution of i-Pr2NH
(6.4 ml) in an argon atmosphere at -78°C, followed by stirring at that temperature for 30
minutes. Methyl acetate (3.6 ml) was added to it, and further stirred for 30 minutes.
Then, a THF solution of the compound (1.9 g) of Reference Example 64 was added to it
and stirred for 2 hours. Water was added to the reaction solution, extracted with ethyl
acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, and
the solvent was evaporated under reduced pressure to obtain the compound (2.8 g) of
Reference Example 121.
Reference Example 122:
6-Fluoro-l-(3-hydroxyethyl)-7-methoxy-2,2-dimethylindan-l-ol:
A THF solution of the compound (1.0 g) of Reference Example 121 was added to
a THF suspension of LiAlH4 (202 mg), followed by heating under reflux at 80°C for 2.5
hours. The reaction solution was cooled, diluted with THF, water (0.8 ml) and an aqueous
15% NaOH solution (0.2 ml) were added thereto and stirred, and the insoluble matter was
removed by filtration using Celite. The solvent was evaporated under reduced pressure,
and tne residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl
acetate = 5/1 to 3/1) to obtain the compound (366 mg) of Reference Example 122.
Reference Example 123:
1 -(1 -Hydroxy-2,2,6-trimethyl-2,3-dihydro-1 H-inden-1 -yl)acetone oxime:
1.58 M n-BuLi/hexane solution (86 ml) was added to a THF solution of acetone
oxime (3.94 g) in an argon atmosphere at 0°C, followed by stirring at that temperature for 2
hours. Next, 2,2,6-trimethylindan-l-one (7.83 g) was added to it, and further stirred for 3
hours. An aqueous saturated ammonium chloride solution was added to the reaction
solution, extracted with ethyl acetate, and washed with water and saturated brine. This
was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure to obtain the compound (12 g) of Reference Example 123.
Reference Example 124:
2^,3',6-Tetramethyl-2,3-dihydro-4rH-spiro[inden-1,5'-isoxazole]:
With cooling on ice, PiOs (60 g) was gradually added to a chloroform solution of
the compound (12 g) of Reference Example 123, followed by stirring at that temperature
for 2 hours. The reaction solution was poured into ice-water, extracted with chloroform,
dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column chromatography (eluent: nhexane/
ethyl acetate = 10/1 to 4/1) to obtain the compound (5.7 g) of Reference Example
124:
[0059]
Reference Example 125:
2,2,3',6-Tetramethyl-2,3-dihydro-4'H-spiro[inden-1,5'-isoxazolidine]:
BFa -EtaO (0.76 ml) was added to a methylene chloride solution of the compound
(1.15 g) of Reference Example 124 in an argon atmosphere at -78°C, followed by stirring at
that temperature for 10 minutes. Then, 0.98 M MeLi/diethyl ether solution (6.12 ml) was
added thereto, followed by stirring at that temperature for 2 hours. An aqueous saturated
sodium hydrogencarbonate solution was added to the reaction solution, and extracted with
chloroform. This was dried over anhydrous sodium sulfate, the solvent was evaporated
under reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: chloroform/ethyl acetate = 2/1) to obtain the compound (421 mg) of Reference
Example 125.
Reference Example 126:
6-Fluoro-7-methoxy-2,2-dimethyl-l-(3-{[(t-butyl)dimethylsilyl]oxy}propyl)indan-l-ol:
In an argon atmosphere, (3-bromopropoxy)(t-butyl)dimethylsilane (3.3 ml) was
dropwise added to a THF suspension of Mg (350 mg), followed by stirring overnight at
room temperature. To this was added a THF solution of the compound (1.0 g) of
Reference Example 64, followed by stirring under heat at 60°C for 1 hour. The reaction
solution was cooled, an aqueous saturated ammonium chloride solution was added thereto,
extracted with ethyl acetate, and dried over anhydrous sodium sulfate. The solvent was
evaporated under reduced pressure, and the residue was purified by silica gel column
chromatography (eluent: n-hexane/ethyl acetate = 10/1) to obtain the compound (865 mg)
of Reference Example 126.
Reference Example 127:
6-Fluoro-1 -(3 -hydoxypropyl)-7-methoxy-2,2-dimethylindan-1 -ol:
1 M n-Bii4NF/THF solution (4.4 ml) was added to a THF solution of the
compound (827 mg) of Reference Example 126, followed by stirring at room temperature
for 2 hours. Water was added to the reaction solution, extracted with ethyl acetate, dried
over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure.
The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl
acetate = 5/1 to 1/1) to obtain the compound (384 mg) of Reference Example 127 as an oil.
[0060]
Reference Example 128:
6-Fluoro-7-methoxy-2,2-dimethyl-1 -(pyridin-2-ylmethyl)indan-l-ol:
2.67 M n-BuLi/hexane solution was added to a THF solution of i-Pr2NH (0.61
ml) in an argon atmosphere at -78°C, followed by stirring for 30 minutes at that
temperature. To it was added 2-picoline (0.43 ml), then heated to room temperature,
followed by stirring for 30 minutes. To it, further added was a THF solution of the
compound (460 mg) of Reference Example 64, followed by stirring at that temperature for
2 hours. Water was added to the reaction solution, extracted with ethyl acetate, washed
with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was
evaporated under reduced pressure, and the residue was purified by silica gel column
chromatography (eluent: n-hexane/ethyl acetate = 5/1) to obtain the compound (525 mg) of
Reference Example 128 as an oil.
Reference Example 129:
4-Fluoro-6,7-dihydroxy-2,2-dimethylindan-1 -one:
With cooling on ice, 1 M BBr3/methylene chloride solution (17 ml) was added to
a 1,2-dichloroethane solution of the compound (1.3 g) of Reference Example 90, followed
by stirring at that temperature for 1 hour. An aqueous saturated sodium
hydrogencarbonate solution was added to the reaction solution, extracted with chloroform,
dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column chromatography (eluent: nhexane/
ethyl acetate = 5/1 to 1/1) to obtain the compound (735 mg) of Reference Example
129.
Reference Example 130:
5-Fluoro-7,7-dimethyl-6,7-dihydro-8H-indano[4,5-d][l,3]dioxol-8-one:
KF (276 mg) and dibromomethane (0.074 ml) were added to a DMF solution of
the compound (200 mg) of Reference Example 129, followed by stirring under heat at
100°C for 5 hours. The reaction solution was concentrated under reduced pressure, then
subjected to liquid-liquid separation with ethyl acetate and an aqueous saturated sodium
hydrogencarbonate solution, and the organic layer was dried over anhydrous sodium
sulfate. The solvent was evaporated under reduced pressure, and the residue was purified
by silica gel column chromatography (eluent: n-hexane/ethyl acetate =5/1) to obtain the
compound (40 mg) of Reference Example 130.
Reference Example 131:
6-Fluoro-8,8-dimethyl-2,3,7,8-tetrahydro-9H-indeno[4,5-b][l,4]dioxin-9-one:
A DMF solution of the compound (251 mg) of Reference Example 129,1,2-
dibromoethane (0.11 ml) and K2CO3 (412 mg) was stirred under heat at 80°C for 4 hours.
The reaction solution was concentrated under reduced pressure, then subjected to liquidliquid
separation with ethyl acetate and an aqueous saturated sodium hydrogencarbonate
solution, the organic layer was dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure. The residue was purified by silica gel column
chromatography (eluent: n-hexane/ethyl acetate = 3/1) to obtain the compound (68 mg) of
Reference Example 131.
In Reference Example 132, the compound in Table 11 was produced in the same
manner as in Reference Example 129 but from the compound of Reference Example 71.
[0061]
Reference Example 133:
4-Fluoro-7-hydroxy-6-iodo-2,2-dimethylindan-1 -one:
The compound (4.26 g) of Reference Example 132 was dissolved hi
trifluoroacetic acid (169 ml) and concentrated sulfuric acid (35 ml), and N-iodosuccinimide
(5.18 g) was added to it at 0°C. This was stirred at that temperature for 1 hour, then water
was added thereto, and extracted with ethyl acetate. This was washed with saturated
brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column chromatography (eluent: nhexane/
ethyl acetate = 10/1) to obtain the compound (6.46 g) of Reference Example 133.
Reference Example 134:
5-Fluoro-7,7-dimethyl-2-(trimethylsilyl)-6,7-dihydro-8H-indene[5,4-b]furan-8-one:
Et3N (43.5 ml), trimethylsilylacetylene (17.3 ml), PdCl2(PPh3)2(548 mg) and Cul
(595 mg) were added to an MeCN solution of the compound (5.0 g) of Reference Example
133, followed by stirring at 50°C for 2 days. The reaction solution was concentrated
under reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: hexane/ethyl acetate = 5/2) to obtain the compound (4.09 g) of Reference Example
134.
In Reference Example 135, in the same manner as in Reference Example 3; in
Reference Example 136, in the same manner as in Reference Example 23; in Reference
Example 137, in the same manner as in Reference Example 27; the compounds shown in
Table 11 were produced.
Reference Example 138:
6-Fluoro-7-(2-hydroxyethoxy)-2,2-dimethylindan-1 -one:
A DMF solution of the compound (500 mg) of Reference Example 83,2-
bromoethanol (0.55 ml) and KiCOs (1.1 g) was stirred under heat at 80°C. After 6 hours,
and after 8 hours, 2-bromoethanol (0.55 ml) was added thereto, followed by stirring
overnight under heat at that temperature. Water was added to the reaction solution,
extracted with ethyl acetate, and washed with water and saturated brine. This was dried
over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent; n-hexane/ethyl acetate
5/1) to obtain the compound (578 mg) of Reference Example 138 as an oil.
Reference Example 139:
1 -(3-Buten-l -yl)-6-fluoro-7-methoxy-2,2-dimethylindan-1 -ol:
In an argon atmosphere, 4-bromo-l-butene (1.5 ml) was drop wise added to a
THF suspension of Mg (350 mg), followed by stirring overnight at room temperature. A
THF solution of the compound (1.0 g) of Reference Example 64 was added to it at room
temperature, followed by stirring under heat at 60°C for 1 hour. An aqueous saturated
ammonium chloride solution was added to the reaction solution, extracted with ethyl
acetate, and dried over anhydrous sodium sulfate. The solvent was evaporated under
reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: n-hexane/ethyl acetate =10/1) to obtain the compound (890 mg) of Reference
Example 139.
Reference Example 140:
2,l'-indene]:
An MeCN solution of the compound (888 mg) of Reference Example 139 was
gradually dropwise added to an acetonitrile solution of iodine (1.7 g) and NaHCO3 (1.5 g),
at room temperature. This was stirred at that temperature for 1 hour, then an aqueous
sodium thiosulfate solution was added to the reaction solution, extracted with ethyl acetate,
washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was
evaporated under reduced pressure, and the residue was purified by silica gel column
chromatography (eluent: n-hexane/ethyl acetate = 20/1) to obtain the compound (985 mg)
of Reference Example 140 as an oil.
Reference Example 141 :
2-(2-Hydroxyethyl)-6-metiiylindan- 1 -one:
A mixture of 34HMeylbenzyl)dihydrofuran-2(3H)one (2.9 g) and TfOH (23 g)
was stirred overnight at 80°C. This was restored to room temperature, then water was
added thereto and extracted with chloroform. The organic layer was dried over anhydrous
sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was
purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate = 1/1) to
obtain the compound (1.4 g) of Reference Example 141.
Reference Example 142:
2-(2-Hydroxyethyl)-2,6-dimethylindan- 1 -one:
55% oily NaH (696 mg) was added to a THF solution of the compound (1.38 g)
of Reference Example 141 at room temperature, followed by stirring for 10 minutes. To it
was added Mel (1 .04 ml), followed by stirring at room temperature for 2 hours. An
aqueous saturated ammonium chloride solution was added to the reaction solution, and
extracted with ethyl acetate. This was dried over anhydrous sodium sulfate, and the
solvent was evaporated under reduced pressure to obtain a mixture of the compound of
Refifence Example 142 and 2-(2-methoxyethyl)-2,6-dimethylindan-l-one. This was
dissolved in 1,2-dichioroethane, and 1 M BBr3/dichloromethane solution (7.3 ml) was
added thereto and stirred at room temperature for 1 hour. An aqueous saturated sodium
hydrogencarbonate solution was added to the reaction solution, extracted with chloroform,
dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column chromatography (eluent: nhexane/
ethyl acetate = 5/2) to obtain the compound (540 mg) of Reference Example 142
and 2-(2-bromoethyl)-2,6-dimethylindan-l-one (1.25 g).
[0063]
Reference Example 143:
N'-[l-(3-butyl-6-fluoro-2-hydroxyphenyl)-2-methylpropylidene]isonicotinohydrazide:
An EtOH suspension of the compound (88 g) of Reference Example 117 and
isonicotinohydrazide (55 g) was heated under reflux for 6 hours. The solvent was
evaporated, water and diethyl ether were added, followed by stirring. The precipitated
matter was collected by filtration, washed with water and diethyl ether, and dried under
reduced pressure to obtain the compound (92) of Reference Example 143 as a crystal.
Reference Example 144:
4-Bromo-7-fluoro-3-hydroxy-2,2-dimethyl-3-(pyridin-4-yl)indan-1 -one:
At room temperature, PhI(OAc)2 (92 g) was added to a 1,2-dichloroethane
solution of the compound (91 g) of Reference Example 143, followed by stirring at that
temperature for 2 hours. An aqueous saturated ammonium hydrogencarbonate solution
was added, followed by stirring. The precipitated matter was removed by filtration using
Celite. The filtrate was subjected to liquid-liquid separation, the organic layer was dried
over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure.
The residue was dissolved in 1,2-dichloroethane, then l,8-diazabicyclo[5,4,0]undec-7-ene
(7.2 ml) was added thereto, followed by stirring under heat at 60°C for 1 hour. The
reaction suspension was cooled to room temperature, the precipitated matter was collected
by miration and washed with a small amount of 1,2-dichloroethane to obtain the compound
(65 g) of Reference Example 144 as a crystal.
[0064]
Example 1:
2,2-Dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol monofumarate:
With cooling on ice, a THF solution of (l-methylpiperidin-4-yl)magnesium
chloride (2 equivalents) that had been separately prepared from 4-chloro-lmethylpiperidine,
Mg (2 equivalents) and EtBr (catalytic amount) was added to a THF (20
ml) solution of 2,2-dimethylindan-l-one (961 mg), followed by stirring for 2 hours at a
temperature falling between that temperature and room temperature. An aqueous
saturated ammonium chloride solution was added to the reaction solution, and the aqueous
layer was extracted with ethyl acetate, washed with saturated brine, and dried over
anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent:
chloroform/methanol/aqueous saturated ammonia = 10/1/0.1) to obtain a colorless crystal
(1.46 g). This was formed into its salt with 1 equivalent of fumaric acid, and washed with
diethyl ether to obtain the compound of Example 1 as a colorless crystal.
In Examples 2 to 5, the compounds shown in Table 12 were produced in the same
manner as in Example 1.
Example 6:
2,2,6-Trimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol monofumarate:
With cooling on ice, a THF solution of (l-methylpiperidin-4-yl)magnesium
chloride (2 equivalents) that had been separately prepared from 4-chloro-lmethylpiperidine,
Mg (2 equivalents) and EtBr (catalytic amount) was added to a THF (100
ml) solution of 2,2,6-trimethylindan-l-one (8.0 g), followed by stirring for 2 hours at a
temperature falling between that temperature and room temperature. An aqueous
saturated ammonium chloride solution was added to the reaction solution, and the aqueous
layer was extracted with ethyl acetate, washed with saturated brine, and dried over
anhfBrous sodium sulfate. The solvent was evaporated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent:
chloroform/methanol/aqueous saturated ammonia = 10/1/0.1) to obtain a colorless crystal
(9.2 g). This was formed into its salt with 1 equivalent of fumaric acid, and recrystallized
from ethanol/ethyl acetate to obtain the compound of Example 6 as a colorless crystal.
In Examples 7 to 12, the compounds shown in Tables 13 and 14 were produced in
the same manner as in Example 6.
[0065]
Example 13:
7-Bromo-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol monofumarate:
The compound (1.93 g) of Example 48 was dissolved in a mixed solvent of THF
(50 ml) and ethyl acetate (50 ml), and i-PrNEt (0.68 ml) and then 10% PD-C (1 g) were
added, and in a hydrogen atmosphere (ordinary pressure), this was stirred at room
temperature for 2 hours. The reaction solution was diluted with ethanol, the insoluble
matter was removed by filtration, and the solvent was evaporated under reduced pressure.
The residue was subjected to liquid-liquid separation with an aqueous saturated sodium
hydrogencarbonate solution and chloroform, the organic layer was dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was
purified by silica gel column chromatography (eluent: chloroform/methanol/aqueous
saturated ammonia = 20/1/0.1) to obtain a crystal (735 mg). This was formed into its salt
with one equivalent of fumaric acid, and recrystallized from EtOH/acetone to obtain the
compound of Example 13 as a colorless crystal.
In Examples 14 to 16, the compounds shown in Table 14 were produced in the
same manner as in Example 6.
Example 17;
6-Cyano-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol monofumarate:
An N-methylpyrrolidone (5 ml) solution of a desalted product (500 mg) of the
compound of Example 14, Zn(CN)2 (191 mg), Pd(PPh3)4 (512 mg) and Ca(OH)2 (121 mg)
was'ltirred under heat at 100°C for 4 hours. The reaction solution was subjected to liquidliquid
separation with chloroform and an aqueous saturated sodium hydrogencarbonate
solution. The organic layer was washed with water and saturated brine, and dried over
anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The
residue was purified by silica gel column chromatography (eluent:
chloroform/methanol/aqueous saturated ammonia = 10/1/0.1) to obtain a crystal (330 mg).
This was formed into its salt with one equivalent of fumaric acid, and washed with diethyl
ether to obtain the compound of Example 17 as a colorless crystal.
In Examples 18 to 62, the compounds shown in Tables 15 to 23 were produced in
the same manner as in Example 6.
[0066]
Example 63:
7-nuoro-33-dimethyl(l-methylpiperidinyl)-l3,4-tetrahydroqiiinolin-4-ol
monofumarate:
With cooling on ice, LiAlKt (302 mg) was added to a THF (30 ml) solution of the
compound (500 mg) of Example 64, followed by heating under reflux for 24 hours. The
reaction solution was cooled with ice, NaaSCVlOttO and Celite were added thereto,
followed by stirring. Then, the insoluble matter was removed by filtration. The solvent
was evaporated under reduced pressure, and the residue was purified by silica gel column
chromatography (eluent: chloroform/methanol/aqueous saturated ammonia = 10/1/0.1) to
obtain an amorphous substance (450 mg). This was formed into its salt with one
equivalent of fumaric acid, and washed with acetone to obtain the compound of Example
63 as a crystal.
In Examples 64 to 70, the compounds shown in Tables 23 and 24 were produced
in the same manner as in Example 6.
In Example 71, the compound shown in Table 24 was produced in the same
manner as in Example 72 given below.
Example 72:
2,2,6-Trimethyl-l -(1 -methylpyrrolidin-3-yl)indan-1 -ol monofumarate:
At -10°C, 1.6 M n-BuLi/hexane solution (3.16 ml) was added to a THF (20 ml)
solution of i-PriNH (0.7 ml), followed by stirring at that temperature for 30 minutes. The
reaction solution was cooled to -78°C, and N-methylpyrrolidone (0.386 ml) was added,
followed by further stirring for 1 hour. A THF (5 ml) solution of 2,2,6-trimethylindan-lone
(450 ml) was added, followed by stirring for 30 minutes, and then heated to -30°C.
Then, an aqueous saturated ammonium chloride solution was added, followed by extraction
with diethyl ether. The organic layer was washed with saturated brine, dried over
anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The
residue was dissolved in THF (50 ml), and LiAlH4 (950 mg) was added thereto, followed
by heating under reflux for 1 hour. With cooling on ice, NaaSO^lO^O and Celite were
added to the reaction solution, followed by stirring. Then, the insoluble matter was
removed by filtration. The solvent was evaporated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent:
chloroform/methanol/aqueous saturated ammonia = 10/1/0.1) to obtain an oil (435 mg).
This was formed into its salt with one equivalent of fumaric acid, and washed with ethyl
acetate to obtain the compound of Example 72 as a colorless crystal.
[0067]
Example 73:
2,2,6-Trimethyl-1 -(piperidin-4-yl)indan-1 -ol monofumarate:
The compound (1.04 g) of Reference Example 68 was dissolved in a mixed
solvent of MeOH (10 ml), EtOH (10 ml) and water (10 ml), and KOH (15 g) was added,
followed by stirring at 80°C for 2 hours. The reaction solution was extracted with ethyl
acetate, washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent
was evaporated under reduced pressure. The residue was purified by silica gel column
chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia = 5/1/0.1) to
obtain an amorphous substance (810 mg). This was formed into its salt with one
equwalent of fumaric acid, and washed with diethyl ether to obtain the compound of
Example 73 as a colorless crystal.
In Examples 74 and 75, the compounds shown in Table 25 were produced in the
same manner as in Example 73.
In Examples 76 and 77, the compounds shown in Table 25 were produced in the
same manner as in Example 78 given below.
Example 78:
2,2,6-Trimethyl-1 -(1 -benzylpiperidin-4-yl)indan-1 -ol monofumarate:
Acetic acid (0.44 ml) was added to a 1,2-dichloroethane (4 ml) solution of a
desalted product (200 mg) of the compound of Example 73 and benzaldehyde (0.157 ml) at
room temperature, followed by stirring for 15 minutes. Then, NaB(OAc)3H (817 mg) was
added, followed by further stirring for 1 hour. An aqueous saturated ammonia was added
to the reaction solution, followed by extraction with ethyl acetate and washing with
saturated brine. This was dried over anhydrous sodium sulfate, the solvent was
evaporated under reduced pressure, and the residue was purified by silica gel column
chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia = 20/1/0.1). This
was formed into its salt with one equivalent of fumaric acid, and washed with diethyl ether
to obtain the compound (178 mg) of Example 78 as a crystal.
In Example 79, the compound shown in Table 26 was produced in the same
manner as in Example 78.
[0068]
Example 80:
4-( 1 -Methoxy-2,2,6-trimethyl-2,3 -dihydro-1 H-inden-1 -yl)-1 -methylpiperidin
monofumarate:
10-Camphorsulfonic acid (255 mg) was added to an MeOH (5 ml) solution of a
desalted product (200 mg) of the compound of Example 6, followed by stirring at room
temperature for 24 hours. The reaction liquid was subjected to liquid-liquid separation
with an aqueous saturated sodium hydrogencarbonate solution and ethvl acetate
orgiRc layer was washed with saturated brine, dried over anhydrous sodium sulfate, and
the solvent was evaporated under reduced pressure. The residue was purified by basic
silica gel column chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia
= 10/1/0.1), then formed into its salt with one equivalent of fumaric acid, and recrystallized
from MeOH/diethyl ether to obtain the compound (151 mg) of Example 80 as a colorless
crystal.
Example 81:
[6-Fluoro-2,2-dimethyl-l-(l-methylpiperidin-4-yl)-2,3-dihydro-lH-inden-l-yl]amine
monofumarate:
10% Pd-C (0.5 g) was added to an MeOH solution of a desalted product (2.29 g)
of the compound of Example 82, and in a hydrogen atmosphere (normal pressure), this was
stirred at room temperature for 20 hours. The insoluble matter was removed by filtration.
The solvent was evaporated under reduced pressure, the residue was purified by silica gel
column chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia =
10/1/0.1), then formed into its salt with one equivalent of fumaric acid, and washed with
diethyl ether to obtain the compound (1.81 g) of Example 81 as a colorless crystal.
[0069]
Example 82:
4-( 1 -Azido-6-fluoro-2,2-dimethyl-2,3-dihydro-1 H-inden-1 -yl)-1 -methylpiperidine
monofumarate:
With cooling on ice, a chloroform solution of trifluoroacetic acid (4.03 ml) and a
desalted product (2.4 g) of the compound of Example 9 was added to a chloroform (15 ml)
solution of NaNs (1.36 g), followed by stirring at room temperature for 4 hours. An
aqueous saturated ammonia was added to the reaction solution, followed by extraction with
chloroform, washing with water, and drying over anhydrous sodium sulfate. The solvent
was evaporated under reduced pressure, and the residue was purified by silica gel column
chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia = 5/1/0.1) to
obtain an oil (2.48 g). This was formed into its salt with one equivalent of fumaric acid,
and flashed with diethyl ether to obtain the compound of Example 82 as an amorphous
substance.
In Examples 83, 84 and 85, the compounds shown in Tables 26 and 27 were
produced in the same manner as in Examples 81, 82 and 6, respectively.
In Example 86, in the same manner as in Example 73; and in Example 87, in the
same manner as in Example 6, the compounds shown in Table 27 were produced.
[0070]
Example 88:
2,2-Dimethyl-1 -(1 -methylpiperidin-4-yl)-6-(piperidin-1 -ylcarbonyl)indan-1 -ol:
An aqueous 10% NaOH solution (17 ml) was added to an MeOH solution of a
desalted product (345 mg) of the compound of Example 17, followed by stirring under heat
at 60°C for 13 hours. After completion of the reaction, this was neutralized with IN
hydrochloric acid to have a pH of from 5 to 6, and the solvent was evaporated under
reduced pressure. Next, the residue was dissolved in DMF, and then piperidine (0.6 ml),
1-hydroxybenzotriazole (164 mg), l-ethyl-3-(3-dimethylaminopropyl)carbodiimide
hydrochloride (232 mg) were added, followed by stirring for 1 day. Water and chloroform
were added to the reaction solution for liquid-liquid separation, the organic layer was
washed with saturated brine, and followed by drying over anhydrous sodium sulfate. The
solvent was evaporated under reduced pressure, and the residue was purified by silica gel
column chromatography (eluent: chloroform/methanol/aqueous saturated ammonia =
20/1/0.1 to 10/1/0.1) to obtain the compound (12 mg) of Example 88 as a colorless
amorphous substance.
Example 89:
Benzyl 3-hydroxy-2,2-dimethyl-3-(l-methylpiperidin-4-yl)indane-5-carboxylate:
An aqueous 10% NaOH solution (8.4 ml) was added to an MeOH solution of a
desalted product (600 mg) of the compound of Example 17, followed by stirring at 70°C for
21 hours. The reaction solution was subjected to liquid-liquid separation with water and
chloroform, the aqueous layer was neutralized with 1 N hydrochloric acid to have a pH of 6
or SCT, and water was evaporated under heat under reduced pressure. The residue was
dissolved in acetonitrile, and with cooling on ice, benzyl alcohol (2.2 ml), N,Ndimethylpyridine-
4-amine (258 mg) and l-ethyl-3-(3-dimethylaminopropyl)carbodiimide
hydrochloride (445 mg) were added thereto, followed by stirring at room temperature for
18 hours. The reaction solution was subjected to liquid-liquid separation with chloroform
and water, and the organic layer was washed with saturated brine, and dried over anhydrous
sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was
purified by silica gel column chromatography (eluent: chloroform/MeOH/aqueous saturated
ammonia = 10/1/0.1) to obtain the compound (8 mg) of Example 89 as a colorless
amorphous substance.
In Example 90, the compound shown in Table 27 was produced in the same
manner as in Example 6.
In Examples 91 and 100, the compounds shown in Tables 28 and 29 were
produced in the same manner as in Example 6 but from the mixture of 4-fluoro-6-hydroxy-
2,2,5-trimethylindan-l-one and 4-fluoro-6-hydroxy-2,2-dimethylindan-l-one obtained in
Reference Example 92.
In Examples 92 to 94, in the same manner as in Example 6; and in Example 95,
in the same manner as in Example 119, the compounds shown in Table 28 were produced.
[0071]
Example 96:
7-Ethyl-5-fluoro-2,2-dimethyl-l -(1 -methylpiperidin-4-yl)indan-1 -ol monofumarate:
In MeOH in the presence of 10% Pd-C in a hydrogen atmosphere having one
atmospheric pressure, a desalted product (27 mg) of the compound of Example 116 was
stirred at room temperature for 5 hours. The insoluble matter was removed by filtration
using Celite. The solvent was evaporated under reduced pressure, and the residue was
formed into its fumarate with one equivalent fumaric acid, and then washed with diethyl
ether to obtain the compound (25 mg) of Example 96 as a colorless powder.
In Example 97, in the same manner as in Example 6 but from the compound of
Reference Example 82; and in Examples 98, 99, 101 and 102, in the same manner as in
Example 6, the compounds shown in Tables 29 and 30 were produced.
Example 103:
5,7-Dibromo-6-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol:
With cooling on ice, SOCk (0.89 ml) was gradually dropwise added to an MeCN
suspension of the compound (1.1 g) of Example 153. This was stirred at that temperature
for 1 hour, then the solvent was evaporated under reduced pressure with cooling with water.
The residue was dissolved in acetic acid, and Zn powder (0.8 g) was added, followed by
stirring under heat at 60°C for 2 hours. Zn was removed by filtration using Celite, acetic
acid was evaporated under reduced pressure, and the residue was subjected liquid-liquid
separation with a diluted aqueous ammonia and chloroform. The chloroform layer was
dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia = 20/1/0.1) to obtain the compound (436
mg) of Example 103 as a colorless amorphous substance.
In Examples 104 to 106, in the same manner as in Example 6; in Example 107, in
the same manner as in Example 119; and in Examples 108 and 109, in the same manner as
in Example 6, the compounds shown in Tables 30 and 31 were produced.
[0072]
Example 110:
A THF solution of a desalted product (207 mg) of the compound of Example 113
was cooled to -70°C, and 1 M i-BuaAlH/toluene solution (3.1 ml) was dropwise added,
followed by stirring at -70°C for 1 hour. Then, it was heated to room temperature, and
further heated for 4 hours. NaiSCVlOHbO was added to the reaction solution and stirred,
then the insoluble matter was removed by filtration using Celite, and the solvent was
evaporated under reduced pressure. The residue was dissolved in MeOH, and with
cooffng on ice, NaBH4 (24 mg) was added thereto, followed by stirring at that temperature
for 30 minutes. The reaction solution was concentrated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia = 10/1/0.1) to obtain the compound (59 mg)
of Example 110 as an amorphous substance.
Example 111:
4-Fluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-6-(morpholin-4-
ylmethyl)indan-1 -ol:
Morpholine (0.07 ml) and i-PraNEt (0.01 ml) were added to a THF suspension of
the compound (30 mg) of Example 112, followed by stirring at room temperature for 7
hours. The reaction solution was concentrated under reduced pressure, and the residue
was purified by silica gel column chromatography (eluent: chloroform/MeOH/aqueous
saturated ammonia = 10/1/0.1) to obtain the compound (12 mg) of Example 111 as a
colorless amorphous substance.
Example 112:
6-Chloromethyl-4-fluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol
hydrochloride:
An MeCN solution of the compound (52 mg) of Example 110 was cooled at 0°C,
and then SOCli (0.06 ml) was gradually added, followed by stirring for 1.5 hours. After
completion of the reaction, the solvent was evaporated under reduced pressure to obtain the
compound (61 mg) of Example 112 as an amorphous substance.
In Example 113, in the same manner as in Example 119; in Example 114, in the
same manner as in Example 6; and in Example 115, as the side product of Example 114,
the compounds shown in Table 32 were produced.
Example 116:
4-Fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-7-vinylindan-1 -ol fumarate:
Water (1 ml) was added to a toluene (2 ml) suspension of the compound (200
mg) of Example 36, 2-vinyl-4,4,5,5-tetramethyl-l,3,2-dioxaborolan (108 mg), Na2CO3 (180
mg) and Pd(PPli3)4 (58 mg), followed by heating overnight under reflux. The reaction
solution was subjected to liquid-liquid separation with chloroform and an aqueous saturated
sodium hydrogencarbonate solution, the organic layer was dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The residue was purified
by silica gel column chromatography (eluent: chloroform/MeOH/aqueous saturated
ammonia = 10/1/0.1), then formed into its fumarate with one equivalent of fumaric acid,
and washed with diethyl ether to obtain the compound of Example 116 as a colorless
powder.
Example 117:
4-Fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-7-phenylindan-1 -ol fumarate:
Water (0.5 ml) was added to a toluene (1 ml) suspension of the compound (102
mg) of Example 36, PhB(OH)2 (43 mg), Na2CO3 (95 mg) and Pd(PPh3)4 (35 mg), followed
by heating under reflux for one day. The reaction solution was subjected to liquid-liquid
separation with chloroform and an aqueous saturated sodium hydrogencarbonate solution,
the organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated
under reduced pressure. The residue was purified by silica gel column chromatography
(eluent: chloroform/MeOH/aqueous saturated ammonia = 10/1/0.1), then formed into its
fumarate with one equivalent of fumaric acid, and recrystallized from isopropanol to obtain
the compound (38 mg) of Example 117 as a colorless crystal.
In Example 118, the compound shown in Table 23 was produced in the same
manner as in Example 117.
Example 119:
7-Cyano-4-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol fumarate:
A l-methyl-2-pyrrolidinone solution of the compound (107 mg) of Example 36,
Zn(CN)2 (47 mg), Pd(PPh3)4 (69 mg) and Ca(OH)2 (30 mg) was stirred under heat at 180°C
for 8 hours. The reaction liquid was cooled, and then subjected to liquid-liquid separation
with chloroform and saturated sodium hydrogencarbonate. The organic layer was dried
over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and
the residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia =10/1/0.1), then formed into its fumarate
with one equivalent of fumaric acid, and washed under heat with MeCN to obtain the
compound (19 mg) of Example 119 as a colorless crystal.
In Examples 120 to 122, in the same manner as in Example 117; in Example 123,
as a side product hi Example 124; and in Example 124, in the same manner as in Example
103, the compounds shown in Table 34 were produced.
[0074]
Example 125:
l-(Aminomethyl)-4-fluoro-7-memoxy-2,2-dimethylindan-l-ol fumarate:
A THF solution of the compound (700 mg) of Reference Example 120 was added
to a THF suspension of LiAlHt (175 mg), followed by stirring under heat at 60°C for 2
hours. The reaction solution was diluted with THF, then water (0.7 ml) and an aqueous
15% sodium hydroxide (0.175 ml) solution were added, followed by stirring. Then, the
insoluble matter was removed by filtration using Celite. The solvent was evaporated
under reduced pressure, the residue was dissolved in THF, and then water (2 ml) and NaF
(200 mg) were added, followed by stirring overnight at room temperature. An aqueous
saturated sodium hydrogencarbonate solution was added to the reaction liquid, followed by
extraction with ethyl acetate, washing with saturated brine, and drying over anhydrous
sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was
purified by silica gel column chromatography (eluent: chloroform/MeOH/aqueous saturated
ammonia = 20/1/0.1), then formed into its fumarate with one equivalent of fumade acid,
and washed with ethyl acetate/MeCN to obtain the compound (72 mg) of Example 125 as a
colorless crystal.
Example 126:
4-Fluoro-7-methoxy-2,2-dimethyl-1 -(dimethylamino)indan-1 -ol fumarate:
Formalin (0.4 ml) and formic acid (0.2 ml) were added to a THF solution of a
desalted product (97 mg) of the compound of Example 125, followed by stirring under heat
at 80°C for 7 hours. The reaction solution was subjected to liquid-liquid separation with
an aqueous saturated sodium hydrogencarbonate solution and ethyl acetate, the organic
layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia = 20/1/0.1), then formed into its fumarate
with one equivalent of fumaric acid, and washed with ethyl acetate/acetone to obtain the
compound (72 mg) of Example 126 as a colorless crystal.
In Examples 127 to 130, the compounds shown in Tables 34 and 35 were
produced in the same manner as in Example 132 but from the compound of Reference
Example 122.
[0075]
Example 131:
1 -(2-Amino-2-methylpropyl)-2,2,6-trimethylindan-1 -ol fumarate:
With cooling on ice, a THF solution of the compound (400 mg) of Reference
Example 125 was added to a THF suspension of LiAlHj (186 mg), followed by stirring at
room temperature for 1 hour. Na2S04'10H2O was added to the reaction solution, followed
by stirring. Then, the insoluble matter was removed by filtration using Celite, and the
solvent was evaporated under reduced pressure. The residue was purified by silica gel
column chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia = 50/1/0.1
to 10/1/0.1), then formed into its fumarate with one equivalent of fumaric acid, and
recrystallized from ethyl acetate/acetone to obtain the compound (128 mg) of Example 131
as a colorless crystal.
Example 132:
6-Fluoro-7-methoxy-2,2-dimethyl-1 -[3-(piperidin-1 -yl)propyl]indan-1 -ol fumarate:
MsCl (0.11 ml) was added to a THE solution of the compound (120 mg) of
Reference Example 127 and i-PraNEt (0.4 ml) at room temperature, followed by stirring at
that temperature for 1 hour. The reaction solution was dried into solid under reduced
pressure, then the residue was dissolved in DMF. Piperidine (0.25 ml) was added,
followed by stirring under heat at 80°C for 3 hours. The reaction solution was subjected
liquid-liquid separation with water and ethyl acetate, and the organic layer was washed with
saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated
under reduced pressure, and the residue was purified by silica gel column chromatography
(eluent: chloroform/MeOH/aqueous saturated ammonia = 20/1/0.1), and then formed into
its fumarate with one equivalent of fumaric acid to obtain the compound (24 mg) of
Example 132 as an amorphous substance.
In Examples 133 and 134, the compounds shown in Tables 35 and 36 were
produced in the same manner as hi Example 132.
Example 135:
6-Fluoro-7-methoxy-2,2-dimethyl-1 -[(1 -methylpiperidin-2-yl)methyl]indan-1 -ol fumarate:
A THF solution of the compound (355 mg) of Reference Example 128 and Mel
(1 ml) was heated under reflux for 1.5 hours. The solvent was evaporated under reduced
pressure, the residue was dissolved in ethanol, then NaBKt (267 mg) was added, followed
by stirring at 60°C for 2 hours. The reaction solution was cooled, an aqueous sodium
hydrogencarbonate solution was added thereto, followed by extraction with ethyl acetate
and drying over anhydrous sodium sulfate. The solvent was evaporated under reduced
pressure, and the residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia = 20/1/0.2). Then, the resulting product
was dissolved in EtOH, followed by stirring overnight in a hydrogen atmosphere (one
atn^pheric pressure) in the presence of 10% Pd-C at room temperature. The insoluble
matter was removed by filtration using Celite, and the solvent was evaporated under
reduced pressure to obtain a product. This was formed into its fumarate with one
equivalent of fumaric acid to obtain the compound (212 mg) of Example 135 as an
amorphous substance.
[0076]
Example 136:
6-Fluoro-7-methoxy-2,2-dimethyl-1 - {5 - [(dimethylamino)methyl] -2-thienyl} -indan-1
fumarate:
1.6 M n-BuLi/hexane solution (0.9 ml) was added to a THF solution of 2-
(dimethylaminomethyl)thiophene (203 mg) in an argon atmosphere at -78°C, followed by
stirring at that temperature for 1 hour. To this was added a THF solution of the compound
(100 mg) of Reference Example 64, followed by further stirring for 1 hour. Water was
added to the reaction solution, followed by extraction with ethyl acetate and drying over
anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia = 20/1/0.1), and then formed into its
fumarate with one equivalent of fumaric acid to obtain the compound (121 mg) of Example
136 as an amorphous substance.
In Examples 137 and 138, the compounds shown in Table 36 were produced in
the same manner as in Example 6.
Example 139:
5-Fluoro-7,7-dimethyl-8-(l-methylpiperidin-4-yl)-2,6,7,8-tetrahydro-2H-indeno[4,5-
b]furan-8-ol fumarate:
10% Pd-C was added to an MeOH solution of a desalted product (500 mg) of the
compound of Example 140, followed by stirring in a hydrogen atmosphere (1 atmospheric
pressure) at room temperature for 5 hours. The insoluble matter was removed by filtration
using Celite, and the solvent was evaporated under reduced pressure. This was formed
i n t e s fumarate with one equivalent of fumaric acid, and then crystallized from THF to
obtain the compound (536 mg) of Example 139 as a colorless crystal.
[0077]
Example 140:
5-Fluoro-7,7-dimethyl-8-(l-methylpiperidin-4-yl)-7,8-dihydro-6H-indeno[4,5-b]furan-8-
fumarate:
A THF solution (20 ml) of 0.7 M (N-methylpiperidin-4-yl)magnesium chloride
was added to a THF solution of the compound (2.0 g) of Reference Example 134, followed
by stirring at room temperature for 1 hour. A THF solution (24 ml) of 1 M (n-BufoNF
was added to it, followed by further stirring at room temperature for 1 hour. An aqueous
saturated ammonium chloride solution was added, followed by extraction with ethyl acetate
and drying over anhydrous sodium sulfate. The solvent was evaporated under reduced
pressure, and the resulting crude product was purified by recrystallization from ethyl
acetate, formed into its fumarate with one equivalent of fumaric acid, and recrystallized
from THF to obtain the compound of Example 140 as a colorless crystal.
In Examples 141 and 142, the compounds shown in Table 37 were produced hi
the same manner as hi Example 6.
Example 143:
4-(9-Fluoro-5,5-dimethyl-2,3,5,6-tetrahydro-4aH-indeno[l,7-ef][l,4]dioxepin-4a-yl-lmethylpiperidine
fumarate:
3N hydrochloric acid (9 ml) and concentrated hydrochloric acid (2.3 ml) were
added to a THF solution of the compound (910 mg) of Example 142, followed by stirring
under heat at 60°C for 3 days. The reaction solution was neutralized with an aqueous
NaOH solution, followed by extraction with ethyl acetate and drying over anhydrous
sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was
purified by silica gel column chromatography (eluent: chloroform/MeOH/aqueous saturated
ammonia = 20/1/0.1), then formed into its fumarate with one equivalent of fumaric acid,
andjlfccrystallized from acetone to obtain the compound (320 mg) of Example 143 as a
colorless crystal.
Example 144:
1 -(e'-fluoro-y'-methoxy dimethyl-Z'^'^.S-tetrahydro-SH-spirotfuran-l, 1 '-inden]-5-yl)-
N,N-dimethylrnethanamine fumarate:
An aqueous 50% MeiNH solution (1 ml) was added to a DMF solution of the
compound (200 g) of Reference Example 140, followed by stirring under heat at 80°C for
hours. The reaction solution was subjected to liquid-liquid separation with water and
ethyl acetate, and the organic layer was washed with saturated brine and dried over
anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the
residue was purified by silica gel column chromatography (eluent:
chloroform/MeOH/aqueous saturated ammonia = 20/1/0.1), and formed into its fumarate
with one equivalent of fumaric acid to obtain the compound (182 mg) of Example 144 as an
amorphous substance.
In Example 145, in the same manner as in Example 144; and in Example 146, in
the same manner as in Example 6, the compounds shown in Table 38 were produced.
[0078]
Example 147:
l-Methyl-4-(7-methyl-2,3,3a,4-tetrahydro-8bH-indeno[l,2-b]furan-8b-yl)piperidine
fumarate:
An aqueous 3N HC1 solution (15 ml) was added to a THF solution of the
compound (1.59 g) of Example 146, and vigorously stirred for 2 hours. An aqueous IN
NaOH solution was added to the reaction solution so as to make it alkaline, followed by
extraction with ethyl acetate and drying over anhydrous sodium sulfate. The solvent was
evaporated under reduced pressure, and this was formed into its fumarate with one
equivalent of fumaric acid, and recrystallized from MeOH/diethyl ether to obtain the
compound (1.41 g) of Example 147 as a colorless crystal.
In Example 148, the compound shown in Table 38 was produced in the same
manner as in Reference Example 149.
Reference Example 149:
4,6-Dibromo-5-fiuoro-3-hydroxy-2,2-dimethyl-3-(l-methylpiperidin-4-yl)indan-l-one:
A 1,2-dichloroethane suspension of the compound (39 g) of Reference Example
96 and PhI(OAc)2 (47 g) was stirred at 40°C for 3 hours. After it was confirmed that the
generation of nitrogen ended completely, saturated sodium hydrogencarbonate and an
aqueous 5% sodium thiosulfate solution were added, followed by stirring for liquid-liquid
separation. The organic layer was dried over anhydrous sodium sulfate, and the solvent
was evaporated under reduced pressure. Then, the residue was dissolved in THF, and t-
BuOK (9.7 g) was added thereto and stirred at 70°C for 3 hours. After completion of the
reaction, the reaction solution was concentrated under reduced pressure, and subjected to
liquid-liquid separation with ethyl acetate and saturated brine. The organic layer was
washed with saturated brine, men dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure. Ethyl acetate (200 ml) and n-hexane (500 ml) were
added to the residue, followed by stirring. Then, the insoluble matter was collected by
filtration, and washed with diethyl ether to obtain the compound (20 g) of Reference
Example 149 as a pale brown powder.
In Example 150, in the same manner as in Example 149; and in Example 151, in
the same manner as in Example 153, the compounds shown in Tables 38 and 39 were
produced.
Example 152:
Cis-7-bromo-4-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indane-1,3 -diol fumarate:
The compound (6.5 g) of Example 11 was dissolved in 2 N hydrochloric acid
(100 ml), followed by heating under reflux for 5 hours. With cooling on ice, this was
neutralized with an aqueous ammonia added thereto, followed by extraction with
chloroform and drying over anhydrous sodium sulfate. Then, the solvent was evaporated
under reduced pressure and isopropanol was added to a mixture of the residue and trans2,3
J||s(benzoyloxy)succinic acid (6.3 g), followed by stirring. The starting trans-diol
precipitated out as a salt, and the precipitate was removed by filtration. The filtrate was
concentrated under reduced pressure, subjected to liquid-liquid separation with diluted an
aqueous ammonia and chloroform, the chloroform layer was dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The residue was formed
into its fumarate with fumaric acid (1.4 g), and crystallized from acetone to obtain the
compound (4.25 g) of Example 152 as a colorless crystal.
[0079]
Example 153:
Trans-5,7-dibromo-6-fluoro-2,2-dimethyl-l-(l-rnethylpiperidin-4-yl)indane-l,3-diol:
A THF (200 ml) suspension of LiAlHt was cooled to -78°C, and with stirring, a
THF (50 ml) solution of the compound (20 g) of Example 149 was dropwise added thereto,
taking 15 minutes. After the addition, the cooling bath was removed, and the reaction
liquid was warmed to 0°C, taking 1 hour. With cooling on ice, Na2SO4»10H2O was
added, followed by stirring. Then, the insoluble matter was removed by filtration using
Celite. The filtrate was distilled under reduced pressure, and the residue was purified by
silica gel column chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia
= 20/1/0.1 to 5/1/0.1) to obtain the compound (3.2 g) of Example 153 as an amorphous
substance.
Example 154:
Trans-7-brorno-4-fluoro-2,2-dimethyl-1 -(1 -methyl-1,2,3,6-tetrahydropyridin-4-yl)indane-
1,3-diol:
Mel (0.52 ml) was added to a THF solution of the compound (1.04 g) of
Reference Example 144, followed by heating under reflux for 6 hours. The solvent was
evaporated under reduced pressure to obtain 4-(7-bromo-4-floro-l-hydroxy-2,2-dimethyl-3-
oxo-2,3-dihydro-lH-inden-l-yl)-l-methylpyridinium iodide (1.46 g) as an amorphous
substance. This was dissolved in MeOH, and at -10°C, NaBRj (545 mg) was added,
followed by stirring at that temperature for 1 hour. The reaction solution was diluted with
and the precipitated matter was collected by filtration to obtain the compound (640
mg) of Example 154 as a colorless crystal.
Example 155:
Cis-7-bromo-4-fluoro-2,2-dimethyl- 1 -( 1 -methyl- 1 ,2,3 ,6-tetrahydropyridin-4-yl)indane- 1 ,3-
diol:
A few drops of water were added to a methanol solution of 4-(7-bromo-4-fluoro-
1 -hydroxy-2,2-dimethyl-3 -oxo-2,3 -dihydro- 1 H-inden- 1 -yl)- 1 -methylpyridinium iodide
(285 mg) obtained in the same manner as in Reference Example 154 and CeCls (858 mg),
followed by stirring, and at -10°C, NaBfLt (132 mg) was added to it and stirred for 3 hours.
Water was added to the reaction solution, followed by extraction with chloroform and
drying over anhydrous sodium sulfate. The solvent was evaporated under reduced
pressure to obtain the compound of Example 155 as a colorless amorphous substance (70
In Example 1 56, the compound shown in Table 40 was produced in the same
manner as in Example 153.
[0080]
Example 157:
3-Hydroxy-2,2-dimethyl-3-(l-methylpiperidin-4-yl)indane-5-carboxylicacid:
An EtOH solution of the compound (31 mg) of Example 89 and 1,4-
cyclohexadiene (0.6 ml) was stirred in an argon atmosphere in the presence of 10% Pd-C at
room temperature for 1 hour. After completion of the reaction, this was filtered using
Celite to remove the insoluble matter, and the solvent was evaporated under reduced
pressure to obtain the compound (24 mg) of Example 157 as a colorless powder.
Example 158:
7-Methoxy-2,2-dimethyl- 1 -(1 -methylpiperidin-4-yl)-6-nitro-l ,2,3,4-tetrahydronaphthalen-
1-olfumarate:
An AcaO (1.0 ml) solution of the compound (100 mg) of Example 54 was cooled
to 0°C, and an Ac2O (1.0 ml) solution of fuming nitric acid (16 mg) was gradually added
thereto, ims was stirred for 30 minutes, then fuming nitric acid (30 mg) was further
added thereto, followed by stirring at that temperature for 30 minutes. Ice-water was
added to the reaction solution, followed by stirring. Then, it was subjected to liquid-liquid
separation with chloroform and an aqueous saturated sodium hydrogencarbonate solution,
and the organic layer was washed with saturated brine. This was dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced pressure to obtain a mixture
of 7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-6-nitro-1,2,3,4-
tetrahydronaphthalen-1 -ol and 7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-8-nitro-
1,2,3,4-tetrahydronaphthalen-l-ol. This was formed into its fumarate with one equivalent
of fumaric acid, and recrystallized from EtOB to obtain the compound of Example 158 as a
colorless crystal.
[0081]
Example 159:
7-Amuio-6-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-1,2,3,4-
tetrahydronaphthalen-1-ol, and
Example 160:
N-[5-hydroxy-2-methoxy-6,6-dimethyl-5-(l-methylpiperidm-4-yl)-5,6,7,8-
tetrahydronaphthalen-l-yl]acetamide:
10% Pd-C was added to an EtOH/ethyl acetate mixed solution of a mixture (779
mg) 6-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-7-nitro-1,2,3,4-
tetrahydronaphthalen-1 -ol and 6-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)-5-nitro-
1,2,3,4-tetrahydronaphthalen-l-ol that had been obtained through nitration of the compound
of Example 55 in the same manner as in Example 158, followed by stirring in a hydrogen
atmosphere (1 atmospheric pressure) at room temperature for 6 hours. After completion
of the reaction, the insoluble matter was removed by filtration using Celite, and the solvent
was evaporated under reduced pressure. The residue was purified by silica gel column
chromatography (eluent: chloroform/MeOH/aqueous saturated ammonia = 10/1/0.1 to
obtain the compound (167 mg) of Example 159 and the compound (230 mg) of Example
160^ amorphous substances. (The formation of the compound of Example 160 would
result from the residual acetic anhydride in the starting compound.)
In Example 161, the compound shown in Table 40 was produced in the same
manner as in Example 126 but from the compound of Example 159.
[0082]
The structural formulae and the physicochemical data of the compounds of the
above Reference Examples and the compounds of the above Examples are shown in the
following Tables 2 to 40. The compounds shown in Tables 41 to 45 may be readily
produced similarly to the above Examples or Production Methods or according to the
modifications apparent to one skilled in the art. The symbols in the Tables have the
following meanings.
Rf. Reference Example
Ex. Example
(Table Removed)
As described hereinabove, the compounds of the present invention have an
NMDA receptor antagonistic activity, and are useful for treatment and prevention of
Alzheimer's disease, cerebrovascular dementia, Parkinson's disease, ischemic apoplexy,
pain, etc., and they have many industrial applications.







We Claim:
1. A cyclic amine and its salt of the following formula (III):
(Formula Removed)
(wherein the symbols have the following meanings:
X1: a bond, or a linear or branched C1-6 alkylene;
Y1: -OH, -O-linear or branched C1-6 alkyl, -NH2 or -N3;
R1 and R2: the same or different, and a halogen atom, or a linear or branched C1-6
alkyl;
R3 to R6 : the same or different, and a hydrogen atom, a halogen atom, a linear or
branched C1-6 alkyl, -O-linear or branched C1-6 alkyl, -OH, -CN, or -CF3;
R7: a hydrogen atom, a linear or branched C1-6 alkyl, -linear or branched C1-6
alkylene-aryl, or -linear or branched C1-6 alkylene-heteroaryl;
R8 to R11: the same or different, and a hydrogen atom, or a linear or branched C1-
6 alkyl;
provided that 6-chloro-2,2-dimethyl-l-(l-methyl-4-piperidinyl)indan-l-ol is
excluded from the compound).
2. The compound and its salt as claimed in claim 1, selected from
2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
2,2,6-trimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
5-bromo-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6-chloro-5-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6-bromo-4-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
7-bromo-6-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
7-bromo-4-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6-fluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
4-fluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
4-fluoro-6-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
7-ethoxy-6-fluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
4-fluoro-6,7-dimethoxy-2,2-dimethyl-l-(l-methylpiperidin-4-yl)indan-l-ol, 5,6-
difluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6-cyano-4-fluoro-7-methoxy-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
7-bromo-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6,7-difluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
6-fluoro-2,2,7-trimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol,
5,6,7-trifluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol, and 4-bromo-6,7-difluoro-2,2-dimethyl-1 -(1 -methylpiperidin-4-yl)indan-1 -ol
3. A pharmaceutical composition comprising the cyclic amine or a salt thereof as
claimed in any one of claims 1 and 2 and a pharmaceutically acceptable excipient as and when used for treating dementia.

Documents:

2013-DELNP-2007-Abstract-(07-07-2011).pdf

2013-delnp-2007-abstract.pdf

2013-DELNP-2007-Claims-(07-07-2011).pdf

2013-DELNP-2007-Claims-(09-02-2012).pdf

2013-delnp-2007-claims.pdf

2013-DELNP-2007-Correspondence Others-(07-07-2011).pdf

2013-DELNP-2007-Correspondence Others-(08-11-2011).pdf

2013-DELNP-2007-Correspondence Others-(09-02-2012).pdf

2013-delnp-2007-correspondence-others 1.pdf

2013-delnp-2007-correspondence-others.pdf

2013-delnp-2007-description (complete).pdf

2013-DELNP-2007-Form-1-(07-07-2011).pdf

2013-delnp-2007-form-1.pdf

2013-delnp-2007-form-18.pdf

2013-DELNP-2007-Form-2-(07-07-2011).pdf

2013-delnp-2007-form-2.pdf

2013-delnp-2007-form-26.pdf

2013-DELNP-2007-Form-3-(07-07-2011).pdf

2013-DELNP-2007-Form-3-(08-11-2011).pdf

2013-delnp-2007-form-3.pdf

2013-DELNP-2007-Form-5-(07-07-2011).pdf

2013-delnp-2007-form-5.pdf

2013-DELNP-2007-GPA-(07-07-2011).pdf

2013-delnp-2007-pct-210.pdf

2013-delnp-2007-pct-304.pdf


Patent Number 251142
Indian Patent Application Number 2013/DELNP/2007
PG Journal Number 09/2012
Publication Date 02-Mar-2012
Grant Date 27-Feb-2012
Date of Filing 15-Mar-2007
Name of Patentee ASTELLAS PHARMA INC.
Applicant Address 3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
Inventors:
# Inventor's Name Inventor's Address
1 SHINGO YAMASAKI C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
2 DAISUKE SUZUKI C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
3 HIROAKI HOSHII C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
4 KYOICHI MAENO C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
5 YOSHITSUGU SHITAKA C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
6 JOTAROU SUZUKI C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
7 SHIGETI KAWABATA C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
8 NOBUYUKI SHIRAISHI C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
9 SATOSHI HAYASHIBE C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
10 TAKATOSHI KANAYAMA C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
11 JUNYA OHMORI C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
12 TAKAHIKO TOBE C/O ASTELLAS PHARMA INC.,3-11, NIHONBASHI-HONCHO 2-CHOME, CHUO-KU, TOKYO 103-8411, JAPAN
PCT International Classification Number C07C 217/54
PCT International Application Number PCT/JP2005/017272
PCT International Filing date 2005-09-20
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 2004-274105 2004-09-21 Japan