Indian Patents
Title of Invention

"DERIVATIVES OF PHOSPHONOOXY QUINAZOLINE"
Abstract Quinu/oline derivatives of formula (I) wherein A is 5-membered heteroaryl containing a nitrogen atom and one or two further nitrogen atoms; compositions containing them, processes for their preparation and their use in therapy.
Full Text PHOSPHONOOXY QUINAZOLINE DERIVATIVES AND THEIR PHARMACEUTICAL USE
The present invention relates to certain quinazoline derivatives for use in the treatment of certain diseases in particular to proliferative disease such as cancer and in the preparation of medicaments for use in the treatment of proliferative disease, to novel quinazoline compounds and to processes for their preparation, as well as pharmaceutical compositions containing them as active ingredient.
Cancer (and other hyperproliferative disease) is characterised by uncontrolled cellular proliferation. This loss of the normal regulation of cell proliferation often appears to occur as the result of genetic damage to cellular pathways that control progress through the cell cycle. In eukaryotes, an ordered cascade of protein phosphorylation is thought to control the cell cycle. Several families of protein kinases that play critical roles in this cascade have now been identified. The activity of many of these kinases is increased in human tumours when compared to normal tissue. This can occur by either increased levels of expression of the protein (as a result of gene amplification for example), or by changes in expression of co activators or inhibitory proteins.
The first identified, and most widely studied of these cell cycle regulators have been the cyclin dependent kinases (or CDKs). Activity of specific CDKs at specific times is essential for both initiation and coordinated progress through the cell cycle. For example, the CDK4 protein appears to control entry into the cell cycle (the GO-G1-S transition) by phosphorylating the retinoblastoma gene product pRb. This stimulates the release of the transcription factor E2F from pRb, which then acts to increase the transcription of genes necessary for entry into S phase. The catalytic activity of CDK4 is stimulated by binding to a partner protein, Cyclin D. One of the first demonstrations of a direct link between cancer and the cell cycle was made with the observation that the Cyclin Dl gene was amplified and cyclin D protein levels increased (and hence the activity of CDK4 increased) in many human tumours (Reviewed in Sherr, 1996, Science 274: 1672-1677; Pines, 1995, Seminars in Cancer Biology 6: 63-72). Other studies (Loda et al., 1997, Nature Medicine 3(2): 231 -234; Gemma et al., 1996, International Journal of Cancer 68(5): 605-11; Elledge et al. 1996, Trends in Cell Biology 6; 388-392) have shown that negative regulators of CDK function are frequently down regulated or deleted in human tumours again leading to inappropriate activation of these kinases.

More recently, protein kinases that are structurally distinct from the CDK family have been identified which play critical roles in regulating the cell cycle and which also appear to be important in oncogenesis. These include the newly identified human homologues of the Drosophila aurora and S.cerevisiae Ipll proteins. The three human homologues of these genes Aurora-A, Aurora-B and Aurora-C (also known as aurora2, auroral and auroraS respectively) encode cell cycle regulated serine-threonine protein kinases (summarised in Adams et al, 2001, Trends in Cell Biology. 11(2): 49-54). These show a peak of expression and kinase activity through G2 and mitosis. Several observations implicate the involvement of human aurora proteins in cancer. The Aurora-A gene maps to chromosome 20ql3, a region that is frequently amplified in human tumours including both breast and colon tumours. Aurora-A may be the major target gene of this amplicon, since Aurora-A DNA is amplified and mRNA overexpressed in greater than 50% of primary human colorectal cancers. In these tumours Aurora-A protein levels appear greatly elevated compared to adjacent normal tissue. In addition, transfection of rodent fibroblasts with human Aurora-A leads to transformation, conferring the ability to grow in soft agar and form tumours in nude mice (Bischoff et al., 1998, The EMBO Journal. 17(11): 3052-3065). Other work (Zhou et al., 1998, Nature Genetics. 20(2): 189-93) has shown that artificial overexpression of Aurora-A. leads to an increase in centrosome number and an increase in aneuploidy, a known event in :he development of cancer. Further work has shown an increase hi expression of Aurora-B Adams et al., 2001, Chromsoma. 110(2):65-74) and Aurora-C (Kimura et al, 1999, Journal jf Biological Chemistry, 274(11): 7334-40) in tumour cells when compared to normal cells.
Importantly, it has also been demonstrated that abrogation of Aurora-A expression and unction by antisense oligonucleotide treatment of human tumour cell lines (WO 97/22702 tnd WO 99/37788) leads to cell cycle arrest and exerts an antiproliferative effect in these amour cell lines. Additionally, small molecule inhibitors of Aurora-A and Aurora-B have ieen demonstrated to have an antiproliferative effect in human tumour cells (Keen et al. 2001 'oster #2455, American Association of Cancer research annual meeting), as has selective brogation of Aurora-B expression alone by siRNA treatment (Ditchfield et al. 2003, journal f Cell Biology, 161(2): 267-280). This indicates that inhibition of the function of Aurora-A ad/or Aurora-B will have an antiproliferative effect that may be useful in the treatment of uman tumours and other hyperproliferative disease. Further, inhibition of Aurora kinases as a therapeutic approach to these diseases may have significant advantages over targeting signalling pathways upstream of the cell cycle (e.g. those activated by growth factor receptor

tyrosine kinases such as epidermal growth factor receptor (EGFR) or other receptors). Since the cell cycle is ultimately downstream of all of these diverse signalling events, cell cycle directed therapies such as inhibition of Aurora kinases would be predicted to be active across all proliferating tumour cells, whilst approaches directed at specific signalling molecules (e.g. EGFR) would be predicted to be active only in the subset of rumour cells which express those receptors. It is also believed that significant "cross talk" exists between these signalling pathways meaning that inhibition of one component may be compensated for by another.
A number of quinazoline derivatives have been proposed hitherto for use in the inhibition of various kinases. For example, WO 96/09294, WO 96/15118 and WO 99/06378 describe the use of certain quinazoline compounds as receptor tyrosine kinase inhibitors, which may be useful in the treatment of proliferative disease and WO 00/21955 discloses certain quinazoline derivatives as inhibitors of the effects of VEGF.
Quinazoline derivatives have also been disclosed for use in the inhibition of Aurora-A kinase. WO 02/00649 discloses quinazoline derivative bearing a 5-membered heteroaromatic ring where the ring is, in particular, substituted thiazole or substituted thiophene and co-pending patent application WO 03/055491 discloses quinazoline derivatives bearing an optionally substituted pyrazole ring. However despite the compounds of WO 02/00649 and WO 03/055491 there still exists the need for further compounds having Aurora kinase inhibitory properties.
The applicants have been successful in finding a novel series of compounds which inhibit the effects of the Aurora kinases and in particular Aurora-A and/or Aurora-B kinase and which have certain properties that make them particularly useful in formulating medicaments for the treatment of disease. In particular the compounds are of use in the treatment of proliferative disease such as cancer occurring as either solid and haematological tumours where Aurora kinases are known to be active, and especially in diseases such as colorectal, breast, lung, prostate, pancreatic or bladder and renal cancer as well as leukaemias and lymphomas.
According to one aspect of the present invention there is provided a compound of formula (I):
(Formula Remove)

formula (I)
wherein A is 5-membered heteroaryl containing a nitrogen atom and optionally containing one or two further nitrogen atoms; X is O, S, S(0), S(O)2 or NR14; mis 0, 1,2 or 3;
Z is a group selected from -NR'R2, phosphonooxy, Cs-gcycloalkyl which Cs-gcycloalkyl is substituted by phosphonooxy or Chalky! substituted by phosphonooxy, and a 4- to 7-membered ring linked via a carbon atom containing a nitrogen atom and optionally containing a further nitrogen atom, which ring may be saturated, partially saturated or unsaturated wherein the ring is substituted on carbon or nitrogen by phosphonooxy or Chalky! substituted by phosphonooxy, and wherein the ring is optionally further substituted on carbon or nitrogen by 1, 2 or 3 halo or Chalky! groups;
R1 is a group selected from -COR8, -CONR8R9 and Ci.6alkyl which C].6alkyl is substituted by phosphonooxy and optionally further substituted by 1 or 2 halo or methoxy groups; R2 is a group selected from hydrogen, -COR10, -CONR10Rn and Ci.6alkyl which Ci_6alkyl is optionally substituted by 1, 2 or 3 halo or Cj^alkoxy groups, -S(O)PRU (where p is 0,1 or 2) or phosphonooxy, or R2 is a group selected from Ca-ealkenyl, C2-6alkynyl, Cs-ecycloalkyl and Cs-gcycloalkylC i^alkyl;
or R1 and R2 together with the nitrogen to which they are attached form a 4- to 7- membered ring optionally containing a further nitrogen atom which ring may be saturated, unsaturated or partially saturated, wherein the ring is substituted on carbon or nitrogen by a group selected from phosphonooxy and Chalky! which Chalky! is substituted by phosphonooxy or-NR8R9, and where the ring is optionally further substituted on carbon or nitrogen by 1,2 or 3 halo or Ci-4alkyl groups;
R3 is a group selected from hydrogen, halo, cyano, nitro, Cj^alkoxy, Ci^alkyl, -OR12, -CHR12R13, -OC(0)R12, -C(0)R12, -NR12C(O)R13, -C(O)NR12R13, -NR12SO2R13 and -NR12R13;
K is hydrogen or a group selected from Chalky!, heteroaryl, heteroarylCi4alkyl, aryl and arylCMalkyl which group is optionally substituted by 1, 2 or 3 substitutents selected from halo, methyl, ethyl, cyclopropyl and ethynyl; R5 is selected from hydrogen, Chalky!, C2wtalkenyl, C2-4alkynyl, Cs-ecycloalkyl and C3.
R6 and R7 are independently selected from hydrogen, halo, Chalky!, C3.6cycloalkyl, hydroxy
and Cj^alkoxy;
R8 is C]_4alkyl substituted by phosphonooxy and optionally further substituted by 1 or 2 halo
or methoxy groups;
R9 is selected from hydrogen and Chalky!;
R10 is selected from hydrogen and Cj^alkyl optionally substituted by halo, Ci^alkoxy, S(O)q
(where q is 0, 1 or 2) or phosphonoxy;
R11, R12, R13 and R14 are independently selected from hydrogen, Ci^alkyl and heterocyclyl;
or a pharmaceutically acceptable salt thereof.
Within the present invention, it is to be understood that, insofar as certain compounds of formula (I) herein defined may exist in optically active or racemic forms by virtue of one or more asymmetric carbon or sulphur atoms, the invention includes in its definition any such optically active or racemic form which possesses Aurora kinase inhibitory activity and in ^articular Aurora-A and/or Aurora-B kinase inhibitory activity. The synthesis of optically ictive forms may be carried out by standard techniques of organic chemistry well known in he art, for example by synthesis from optically active starting materials or by resolution of a acemic form. Similarly, the above-mentioned activity may be evaluated using the standard iboratory techniques referred to hereinafter.
Within the present invention it is to be understood that a compound of formula (I) or a lit thereof may exhibit the phenomenon of tautomerism and mat the formulae drawings ithin this specification can represent only one of the possible tautomeric forms. It is to be understood that the invention encompasses any tautomeric form which has Aurora kinase inhibitory activity and in particular Aurora-A and/or Aurora-B kinase inhibitory activity and is not to be limited merely to any one tautomeric form utilised within the formulae drawings. It is also to be understood that certain compounds of formula (I) and salts thereof can exist in solvated as well as unsolvated forms such as, for example, hydrated forms. It is to t>e understood that the invention encompasses all such solvated forms which have Aurora kinase inhibitory activity and in particular Aurora-A and/or Aurora-B kinase inhibitory activity-
The present invention relates to the compounds of formula (I) as herein defined as well as to the salts thereof. Salts for use in pharmaceutical compositions will be pharmaceutically acceptable salts, but other salts may be useful in the production of the compounds of formula (I) and their pharmaceutically acceptable salts. Pharmaceutically acceptable salts of the invention may, for example, include acid addition salts of compounds of formula (I) as herein defined which are sufficiently basic to form such salts. Such acid addition salts include but are not limited to furmarate, methanesulphonate, hydrochloride, hydrobromide, citrate and maleate salts and salts- formed with phosphoric and sulphuric acid, fn addition where compounds of formula (I) are sufficiently acidic, salts are base salts and 3xamples include but are not limited to, an alkali metal salt for example sodium or potassium, m alkaline earth metal salt for example calcium or magnesium, or organic amine salt for ;xample triethylamine, ethanolamine, diethanolamine, triethanolamine, morpholine, N-methylpiperidine, j¥-ethylpiperidine, dibenzylamine or amino acids such as lysine.
The compounds of formula (I) may also be provided as in vivo hydrolysable esters. An in vivo hydrolysable ester of a compound of formula (I) containing carboxy or hydroxy group is, for example a pharmaceutically acceptable ester which is cleaved in the human or animal body to produce the parent acid or alcohol. Such esters can be identified by administering, for example, intravenously to a test animal, the compound under test and subsequently examining the test animal's body fluid.
Suitable pharmaceutically acceptable esters for carboxy include Ci-6alkoxyniethyJ esters for example methoxymethyl, Ci-ealkanoyloxymethyl esters for example pivaloyloxymethyl, phthalidyl esters, Ca-gcycloalkoxycarbonyloxyCi-galkyl esters for example 1-cyclohexylcarbonyloxyethyl, l,3-dioxolen-2-onylmethyl esters for example 5-methyl-l,3-dioxolen-2-onyhnethyl, and Ci-ealkoxycarbonyloxyethyl esters for example 1-methoxycarbonyloxyethyl; and may be formed at any carboxy group in the compounds of this invention.
Suitable pharmaceutically acceptable esters for hydroxy include inorganic esters such as phosphate esters (including phosphoramidic cyclic esters) and a-acyloxyalkyl ethers and related compounds which as a result of the in vivo hydrolysis of the ester breakdown to give the parent hydroxy group/s. Examples of a-acyloxyalkyl ethers include acetoxymethoxy and 2,2-dimethylpropionyloxymethoxy. A selection of in vivo hydrolysable ester forming groups for hydroxy include Cj-i0alkanoyl, for example formyl, acetyl, benzoyl, phenylacetyl, substituted benzoyl and phenylacetyl; Ci-i0alkoxycarbonyl (to give alkyl carbonate esters), for
example ethoxycarbonyl; di-Ci-4alkylcarbamoyl and7/-(di-Ci-4alkylaminoethyl)-7V-Ci-4alkylcarbamoyl (to give carbamates); di-Ci-4alkylaminoacetyl and carboxyacetyl. Examples of ring substituents on phenylacetyl and benzoyl include arninomethyl, Q. 4alkylaminoniethyl and di-(Ci-4alkyl)aminomethyl, and morpholino or piperazino linked from a ring nitrogen atom via a methylene linking group to the 3- or 4- position of the benzoyl ring. Other interesting in vivo hydrolysable esters include, for example, RAC(O)OCi-6alkyl-CO-, wherein RA is for example, benzyloxy-Ci-4alkyl, or phenyl. Suitable substituents on aphenyl group in such esters include, for example, 4-Ci-4piperazino-C]-4alkyl, piperazino-Ci-4alkyl and morpholino-Ci-4alkyl.
In this specification the generic term "alky!" includes both straight-chain and branched-chain alkyl groups. However references to individual alky! groups such as "propyl" are specific for the straight chain version only and references to individual branched-chain alkyl groups such as "tert-butyl" are specific for the branched chain version only. An analogous convention applies to other generic terms, for example "alkenyl" and "alkynyl".
"Cycloalkyl" is a monocyclic, saturated alkyl ring and "aryl" is a monocyclic or bicyclic aromatic ring.
Unless otherwise specified "heteroaryl" is a monocyclic or bicyclic aromatic ring containing 5 to 10 ring atoms of which 1, 2, 3 or 4 ring atoms are chosen from nitrogen, sulphur or oxygen where a ring nitrogen or sulphur may be oxidised.
"Heterocyclyl" is a saturated, unsaturated or partially saturated monocyclic or bicyclic ring containing 4 to 12 atoms of which 1, 2, 3 or 4 ring atoms are chosen from nitrogen, sulphur or oxygen, which ring may be carbon or nitrogen linked, wherein a -CH;-group can optionally be replaced by a -C(O)-; wherein a ring nitrogen or sulphur atom is optionally oxidised to form the N-oxide or S-oxide(s); wherein a ring -NH is optionally substituted by acetyl, formyl, methyl or mesyl; and wherein a ring is optionally substituted by one or more halo.
"Phosphonooxy" is in one aspect a group of formula -OP(0)(OH)2- However the term "phosphonooxy" also includes salts of this group such as those formed with alkali metal ions such as sodium or potassium ions or alkaline earth metal ions, for example calcium 01 magnesium ions.
Where optional substituents are chosen from "1 or 2", from "1, 2, or 3" or from "1,2, 3 or 4" groups or substituents it is to be understood that this definition includes all substituents being chosen from one of the specified groups i.e. all substitutents being the sane
or the substituents being chosen from two or more of the specified groups i.e. the substitutents not being the same.
Compounds of the present invention have been named with the aid of computer software (ACD/Name version 6.6 or ACD Name Batch version 6.0).
Suitable values for any R group (R1 to R14) or any part or substitutent for such groups include:
for CMalkyl: methyl, ethyl, propyl, isopropyl, butyl, 2-methylpropyl and /erf-butyl;
for Ci-ealkyl: Chalky!, pentyl, 2,2-dimethylpropyl, 3-methylbutyl and hexyl;
for C2^alkenyl: vinyl, allyl and 1-propenyl;
for Ca-ealkenyl: Ca^alkenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylbut-2-enyl, 3-
methylbut-1-enyl, 1-pentenyl, 3-pentenyl and 4-hexenyl;
for Ci^alkynyl: ethynyl, 1-propynyl, 2-propynyl and 3-burynyl;
for Cj-ealkynyl: Cz^alkynyl, 2-pentynyl, hexynyl and l-rnethylpent-2-ynyl;
for Ca-ecycloalkyl: cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl; for Ca-ecycloalkylCMalkyl: cyclopropyhnethyl, cyclopropylethyl, cyclobutyhnethyl,
cyclopentylmethyl and cyclohexyhnethyl;
for aryl: phenyl and naphthyl;
for arylC]_4alkyl: benzyl, phenethyl, naphthyhnethyl and naphthylethyl;
for halo: fluoro, chloro, bromo and iodo;
for Ci-4alkoxy: methoxy, ethoxy, propoxy and isopropoxy;
for Q-ealkoxy: C]_4alkoxy, pentyloxy, 1-ethylpropoxy andhexyloxy;
for heteroaryl: pyridyl, imidazolyl, quinolinyl, cinnolyl, pyrimidinyl, thiophenyl,
pyrrolyl, pyrazolyl, thiazolyl, triazolyl, oxazolyl, isoxazolyl and
pyrazinyl and preferably thiazolyl, pyridyl, imidazolyl and pyrimidinyl;
for heteroarylC]^alkyl: pyridylmethyl, pyridylethyl, pyrimidinylethyl,
pyrimidinylpropyl, pyrimiduiylbutyl, imidazolylpropyl, imidazolylbutyl, quinolinylpropyl, 1,3,4-triazolylpropyl and oxazolylrnethyl;
for heterocyclyl: furyl, thienyl, pyrrolyl, pyrrolidinyl, imidazolyl, triazolyl, thiazolyl, tetrazolyl, oxazolyl, isoxazolyl, pyrazolyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, quinolinyl, isoquinolinyl, quinoxalinyl, benzothiazolyl, benzoxazolyl, benzothienyl, benzofuryl, piperidinyl, TV-acetylpiperidinyl, A'-methylpiperidinyl, N-
formylpiperazinyl, JV-mesylpiperazinyl, homopiperazinyl, piperazinyl, azetidinyl, oxetanyl, morpholinyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, indolinyl, pyranyl, dihydro-J^-pyranyl, tetrahydrofuranyl, 2,5-dioximidazalidinyl, 2,2-dimethyl-l,3-dioxolanyl and 3,4-dimethylenedioxybenzyl.
It should be noted that examples given for terms used in the description are not limiting.
Preferred values of A, X, m, Z, R3, R4, R5, R6 and R7 are as follows. Such values may be used where appropriate with any of the definitions, claims or embodiments defined herein.
hi one aspect of the invention A is pyrrolyl, pyrazolyl, imidazolyl or triazolyl. In a further aspect A is a group of formula (a), (b), (c), (d) or (e): (Formula Remove)

where * is the point of attachment to the X group of formula (I) and ** is the point of attachment to the (CR R7) group of formula (I). In a preferred aspect A is pyrazolyl. hi j more preferred aspect A is a group of formula (a) as defined above.
hi one aspect of the invention X is NR1 t O or S. hi another aspect X is NR14. In yst another aspect X is NH.
hi one aspect of the invention m is 1, 2 or 3. hi one aspect m is 1 or 2. In another aspect m is 0, 2 or 3. hi another aspect m is 0, 1 or 2. In yet another aspect m is 1. hi a further aspect m is 2.
hi one aspect of the invention Z is -NR]R2 or a 5- to 6-membered saturated ring lilted via a carbon atom containing a nitrogen atom and optionally containing a further nitrogen
atom, which ring is substituted on carbon or nitrogen by phosphonooxy or Ci_4alkyl substituted by phosphonooxy. In another aspect Z is -NB^R2.
In one aspect of the invention R1 is Ci-salkyi substituted by phosphonooxy. In another aspect R1 is Ci.salkyi substituted by phosphonooxy and further substituted by 1 or 2 halo. In a further aspect R1 is 2-phosphonooxyethyl, 2-phosphonooxy-l,l-dimethylethyl, 2-phosphonooxy-2-methylethyl, 3 -phosphonooxy-1,1 -dimethylpropyl, 3 -phosphonooxypropyl and 4-phosphonooxybutyl. In yet another aspect R1 is 2-phosphonooxyethyl, 2-phosphonooxy-l,l-dimethylethyl, 3-phosphonooxy-1,1-dimethylpropyl or 3-phosphonooxypropyl. In yet another aspect R1 is 2-phosphonooxyethyl.
In one aspect of the invention R2 is selected from hydrogen and Cj-ealkyl which Ci_ ealkyl is optionally substituted by 1, 2 or 3 halo or Ci^alkoxy groups, or R2 is selected from C2-6alkenyl, Ca-ealkynyl, C3.6cycloalkyl and Ca-ecycloalkylCMalkyl. In another aspect R2 is hydrogen, allyl, 2-propynyl, methyl, ethyl, propyl, isopropyl, 2-methylpropyl, butyl, 2,2-dimethylpropyl, cyclopropyl, cyclopropylmethyl, cycloburyl, cyclobutylmethyl, cyclopentyl, cyclopentylmethyl, 3,3,3-trifluoropropyl or 2-methoxyethyl.
In one aspect of the invention R1 and R2 together with the nitrogen to which they are attached form a saturated 5- to 6-membered ring optionally containing a further nitrogen atom wherein the ring is substituted on carbon or nitrogen by a group selected from phosphonooxy and Cj^alkyl which Chalky! is substituted by phosphonooxy or -NR8R9, and where the ring is optionally further substituted on carbon or nitrogen by 1 or 2 Chalky! groups. In another aspect of the invention R1 and R2 together with the nitrogen to which they are attached form a piperidine, pyrrolidine or piperazine ring which is substituted by a group selected from phosphonooxy, phosphonooxymethyl, 2-phosphonooxyethyl, 7V-ethyl-JV-(2-phosphonooxyethyl)aminornethyl and //-(2-phosphonooxyethyl)aniinomethyl and where the ring is optionally further substituted by 1 or 2 methyl. In a further aspect of the invention R1 arid R2 together with the nitrogen to which they are attached form 4-(phosphonooxymethyl)piperidinyl, 2-(phosphonooxymethyl)pyrrolidinyl, 4-(2 -phosphonooxyethyl)piperazinyl, 3-(phosphonooxy)pyrrolidinyl, 3-
(phosphonooxy)piperidinyl, 2-[//-ethyl-JV-(2-phosphonooxyethyl)aminomethyl]pyrrolidinyl, 4-(phosphonooxy)piperidinyl, 2-[Ar-(2-phosphonooxyethyl)arriinomethyl]pyrrolidinyl, 4-(2-_3hosphonooxyethyl)piperidinyl, 2-(2-phosphonooxyethyl)pyrrolidinyI and 2-(2-phosphonooxyethyl)piperidinyl. In yet another aspect R1 and R2 together with the nitrogen to which they are attached form 4-(phosphonooxyniethyl)piperidinyl, 2-
(phosphonooxymethyl)pyrroh'dinyl, 2-(2-phosphonooxyethyl)pyrrolidinyl and 3-(phosphonooxy)piperidinyl. In a further aspect R1 and R2 together with the nitrogen to which they are attached form 2-(phosphonooxymethyl)pyrrolidinyl.
In one aspect of the invention R3 is Cj^alkoxy, halo or hydrogen. In a further aspect R3 is Cualkoxy or hydrogen. In another aspect R3 is methoxy. In another aspect R3 is hydrogen. In yet a further aspect R3 is fluoro.
In one aspect R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro. In another aspect R is 3-fluorophenyl, 3-chlorophenyl, 3,5-difluorophenyl, 3,4-difluorophenyl, 2-fiuorophenyl, 2,3-difluorophenyl, 2,4-difluorophenyl and 2,5-difluorophenyl. In a further aspect R4 is 3-fluorophenyl, 3,5-difluorophenyl and 2,3-difluorophenyl. In one aspect R4 is 3-fluorophenyl. In a further aspect R4 is 3,5-difluorophenyl. m yet another aspect R4 is 2,3-difluorophenyl.
In one aspect of the invention R5 is hydrogen or methyl. In another aspect R5 is hydrogen.
hi one aspect of the invention R6 is hydrogen, fluoro, chloro or methyl. In another aspect R6 is hydrogen.
hi one aspect of the invention R7 is hydrogen, fluoro, chloro or methyl, hi another aspect R7 is hydrogen.
In one aspect R8 is 2-phosphonooxyethyl. In one aspect of the invention R9 is hydrogen, methyl or ethyl. In one aspect of the invention R10 is hydrogen, methyl or ethyl, hi one aspect of the invention R11 is hydrogen, methyl or ethyl. In one aspect of the invention R12 is hydrogen or methyl. In one aspect of the invention R13 is hydrogen or methyl, hi one aspect of the invention R14 is hydrogen or methyl. A preferred class of compounds is of formula (I) wherein: A is a group of formula (a), (b), (c), (d) or (e) as defined above; X is NH; mis 0,1,2 or 3;
Z is -NR!R2 or a 5- to 6-membered saturated ring linked via a carbon atom containing a nitrogen atom and optionally containing a further nitrogen atom, which ring is substituted on carbon or nitrogen by phosphonooxy or Ci-4alkyl substituted by phosphonooxy; R1 is Ci-salkyl substituted by phosphonooxy;
R2 is selected from hydrogen and Ci-galkyl which Ci.6alkyl is optionally substituted by 1, 2 or 3 halo or Q^alkoxy groups or R2 is selected from C2-6alkenyl, C2-6alkynyl, Cs-ecycloalkyl and
or R1 and R2 together with the nitrogen to which they are attached form a saturated 5- to 6-membered ring optionally containing a further nitrogen atom wherein the ring is substituted on carbon or nitrogen by a group selected from phosphonooxy and Chalky! which Chalky!
B O
is substituted by phosphonooxy or -NR R , and where the ring is optionally further
substituted on carbon or nitrogen by 1 or 2 Ci^alkyl groups;
R3 is Ci^alkoxy, halo or hydrogen;
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro;
R5 is hydrogen or methyl; and
R6 and R7 are independently hydrogen, fluoro, chloro or methyl;
or a pharmaceutically acceptable salt thereof.
A preferred class of compounds is of formula (I) wherein: A is a group of formula (a), .(b), (c), (d) or (e) as defined above; X is NH; mis 1, 2 or 3; Zis-NR'R2;
R1 is Ci-salkyl substituted by phosphonooxy;
R2 is selected from hydrogen and Ci-ealkyl which Chalky! is optionally substituted by 1, 2 or 3 halo or Ci^alkoxy groups, or R2 is selected from C2-6alkenyl, Ca-ealkynyl, and Cs-ecycloalkylCj^alkyl; R3 is Ci^alkoxy, halo or hydrogen;
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro; R5 is hydrogen or methyl; and
R6 and R7 are independently hydrogen, fluoro, chloro or methyl; or a pharmaceutically acceptable salt thereof.
Another preferred class of compounds is of formula (I) wherein: A is a group of formula (a) as defined above; XisNH; mis 1, 2 or 3; Zis-NR!R2; R1 is d-salkyl substituted by phosphonooxy;

R2 is selected from hydrogen and d-ealkyl which Ci.6alkyl is optionally substituted by 1,2 or
3 halo or C^alkoxy groups, or R2 is selected from Ca-ealkenyl, Ci-ealkynyl, Ca-ecycloalkyl
and Cs-ecycloalkylCMalkyl;
R3 is Cj^alkoxy, halo or hydrogen;
R is phenyl optionally substituted by 1 or 2 of fluoro or chloro;
R5 is hydrogen; and
R6 and R7 are each hydrogen;
or a pharmaceutically acceptable salt thereof.
Yet another preferred class of compounds is of formula (I) wherein:
A is a group of formula (a) as defined above;
X is NH;
m is 1 or 2;
Z is -NR'R2;
R1 is Ci-salkyl substituted by phosphonooxy;
R2 is selected from hydrogen and Ci^alkyl which Chalky! is optionally substituted by 1,2 or
3 halo or Cj^alkoxy groups, or R2 is selected from C2-6alkenyl, C2.6alkynyl, C3^cycloalkyl
and
R3 is
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro;
R5 is hydrogen; and
R5 and R7 are each hydrogen; .
or a pharmaceutically acceptable salt thereof.
A further preferred class of compounds is of formula (I) wherein: A is a group of formula (a) as defined above; X is NH; m is 1,2 or 3; Z is -NR'R2;
R1 is Ci-salkyl substituted by phosphonooxy;
R2 is selected from hydrogen and Ci-ealkyl which Cj-ealkyl is optionally substituted by 1, 2 or 3 halo or Ci^alkoxy groups, or R2 is selected from C2-6alkenyl, Ca-ealkynyl, Cs^cycloalkyl and Ca-scycloalkylCi^alkyl; R3 is hydrogen; R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro;

R5 is hydrogen; and
R6 and R7 are each hydrogen;
or a pharmaceutically acceptable salt thereof.
A further preferred class of compounds is of formula (I) wherein: J A is a group of formula (a) as defined above; XisNH; m is 1 or 2; Zis-NR'R2;
R! is Ci-salkyl substituted by phosphonooxy;
R2 is selected from hydrogen and Chalky! which Chalky! is optionally substituted by 1, 2 or 3 halo or C^alkoxy groups, or R2 is selected from Ca-galkenyl, Ca-galkynyl, Cs-gcycloalkyl and Ca-ecycloalkylCMalkyl; R3 is fluoro;
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro; R5 is hydrogen; and R6 and R7 are each hydrogen; or a pharmaceutically acceptable salt thereof.
Another preferred class of compounds is of formula (I) wherein: A is a group of formula (a), (b), (c), (d) or (e) as defined above; X is NH; m is 0, 1 or 2; Zis-NR'R2
R1 and R2 together with the nitrogen to which they are attached form a saturated 5- to 6-membered ring optionally containing a further nitrogen atom which ring is substituted by a group selected from phosphonooxy and CMalkyl which Ci^alkyl is substituted by phosphonooxy or -NR8R9, and where the ring is optionally further substituted by 1 or 2 Q. 4alkyl groups;
R3 is Ci^alkoxy., halo or hydrogen;
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro; R5 is hydrogen or methyl; and
R6 and R7 are independently hydrogen, fluoro, chloro or methyl; R8 is 2-phosphonooxyethyl; and R9 is hydrogen, methyl or ethyl;
or a pharmaceutically acceptable salt thereof.
A further preferred class of compounds is of formula (I) wherein: A is a group of formula (a) as defined above; X is NH; m is 0, 1 or 2; Zis-NR!R2
R1 and R2 together with the nitrogen to which they are attached form a saturated 5- to 6-membered ring optionally containing a further nitrogen atom wherein the ring is substituted on carbon or nitrogen by a group selected from phosphonooxy and C^aUcyl which C^alkyl is substituted by phosphonooxy or ~NR8R9, and where the ring is optionally further substituted on carbon or nitrogen by 1 or 2 Ci_4alkyl groups; R3 is Ci^alkoxy, halo or hydrogen;
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro; R5 is hydrogen or methyl; and
R6 and R7 are independently hydrogen, fluoro, chloro or methyl; R8 is 2-phosphonooxyethyl; and R9 is hydrogen, methyl or ethyl; or a pharmaceutically acceptable salt thereof.
A further preferred class of compounds is of formula (I) wherein: A is a group of formula (a) as defined above; X is NH; ai is 0, 1 or 2;
I is -NR]R2
II and R2 together with the nitrogen to which they are attached form a saturated 5- to 6-
membered ring optionally containing a further nitrogen atom wherein the ring is substituted
on carbon or nitrogen by a group selected from phosphonooxy and Cj^alkyl which
is substituted by phosphonooxy or -NR8R9, and where the ring is optionally further
substituted on carbon or nitrogen by 1 or 2 Ci_4alkyl groups;
R3 is CMalkoxy;
R4 is phenyl optionally substituted by 1 or 2 of fluoro or chloro;
R5 is hydrogen; and
R6 and R7 are each hydrogen;
El8 is 2-phosphonooxyethyl; and
R9 is hydrogen, methyl or ethyl;
or a pharmaceutically acceptable salt thereof.
A further preferred class of compounds is of formula (I) wherein:
A is a group of formula (a) as defined above;
XisNH;
m is 0, 1 or 2;
Z is -NR'R2
R1 and R2 together with the nitrogen to which they are attached form a saturated 5- to 6-
membered ring optionally containing a further nitrogen atom wherein the ring is substituted
on carbon or nitrogen by a group selected from phosphonooxy and Chalky! which Chalky!
is substituted by phosphonooxy or-NR8R9, and where the ring is optionally further
substituted on carbon or nitrogen by 1 or 2 Q -4alkyl groups;
R3 is hydrogen;
R4 is phenyl optionally substituted by 1 or 2 of fJuoro or chloro;
R5 is hydrogen; and
R6 and R7 are each hydrogen;
R8 is 2-phosphonooxyethyl; and
R9 is hydrogen., methyl or ethyl;
or a pharmaceutically acceptable salt thereof.
hi another aspect of the invention, a preferred compound of the invention is any compound selected from:
{l-[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-ljy-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]piperidin-4-yl}methyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)arnino]-2-oxoemyl}-lH-pyrazol-3-yl)ammo]-6-rnethoxyquinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate; {(25}-l-[3-({4-[(5-{2-[(3,5-difluorophenyl)animo]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; {(2K>l-[3-({4-[(5-{2-[(3,5-difluorop^^
methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; {(2S)-l -[3-( (4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-yl)araino]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl} methyl dihydrogen phosphate; 2-[[3 yl)aniino]-6-methoxyquinazolin-7-yl} oxy)propyl]amino) ethyl dihydrogen phosphate; 1 -[3-( {4-[(5- {2-[(3 -fluorophenyl)amino]-2-oxoethyl} -lfl-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]piperidin-3-yl dihydrogen phosphate; {(2^)-l-[3-({4-[(5-{2-[(23-a^fluorophenyl)amino]-2-oxoethyl}-m-pyrazol-3-yl)arnino]-6-
methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; 2-[[3 yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJ?-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](3,3,3-trifluoropropyl)amino]ethyl dihydrogen phosphate;
2-{allyl[3 2-{cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lF-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]amino) ethyl dihydrogen phosphate; 2-{cyclopropyl[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazoIin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; 2-{(cyclopropylmethyl)[3-({4-[(5-{2-[(253-difluorophenyl)amino]-2-oxoethyl}-lfi-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]ainino} ethyl dihydrogen phosphate and 2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof.
A more preferred compound of the invention is any compound selected from: 2-{4-[({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amiao] quinazolin-7-yl} oxy)methyl]piperidin-1 -yl} ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lflr-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)arnino]-2-oxoethyl}4^-pyrazol-3-yl)amino]-.quinazolin-7-yl)oxy)propyl](isopropyl)amino]ethyl dihydrogen phosphate; 3-{[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-m-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino}-3-methylbutyl dihydrogen phosphate; 2- {(2S)-1 -[3-({4-[(5~ {2-[(2,3-difluorophenyl)amino]-2-oxoethyl}- l#-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl} ethyl dihydrogen phosphate; {(2^)-l-[3-({4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoe%l}-m-pyrazol-3-yl)arnino]-quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl} methyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](propyl)amino]ethyl dihydrogen phosphate; 2-[[3 2- {cyclopentyl[3-( {4-[(5 - {2-[(3-fluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJ?-pyrazol-3-yl)a]iiino]-qumazoliQ-7-yl}oxy)propyl](ethyl)amino] ethyl dihydrogen phosphate;
2-{[3-({4-[(5-{2-[(3-fluorophenyl)arnino]-2-oxoelhyl}-lH-pyTazol-3-yl)amino]quinazolin-7-yl} oxy)propyl] amino} -2-methylpropyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lI/-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](propyl)amino] ethyl dihydrogen phosphate;
{(2/Z)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl} methyl dihydrogen phosphate;
3-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l/]r-pyrazol-3-yl)amino]-quinazolin-7-
yl}oxy)propyl](ethyl)amino]propyl dihydrogen phosphate
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoetliyl}-lfl-pyrazol-3-yl)amino]quinazolin-7-
yl}oxy)propyl](2-methoxyethyl)amino] ethyl dihydrogen phosphate
2-[[4-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)arnino]-
quinazolin-7-yl}oxy)butylJ(propyl)arnino]ethyl dihydrogen phosphate;
2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoeihyl}-lH-pyrazol-3-yl)arnino]-
quinazolin-7-yl}oxy)butyl](ethyl)amino]ethyl dihydrogen phosphate;
{(27?)-l-[4-({4-[(5-{2-[(23-difliiorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-
quinazolin-7-yl) oxy)butyl]pyrrolidin-2-yl} methyl dihydrogen phosphate;
2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/ir-pyrazol-3-
yl)amino]quinazolin-7-yl} oxy)butyl](methyl)amino]ethyl dihydrogen phosphate; and
{(26)-l-[4 quinazolin-7-yl} oxy)butyl]pyrrolidin-2-yl} methyl dihydrogen phosphate;
or a pharmaceutically acceptable salt thereof.
A further preferred compound is:
2- {ethyl[3-( {6-fluoro-4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof.
A more preferred compound is any compound selected from: {l_[3_({4_[(5-{2-[(3-fluorophenyl)ammo]-2-oxoemyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl) oxy)propyl]piperidin-4-yl}methyl dihydrogen phosphate;
(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl}-l jy-pyrazol-3-yl)amino]-6-methoxyquinazolhi-7-yl} oxy)propyl]pyrrolidin-2-yl}methyI dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l/^pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](isobutyl)amino]ethyl dihydrogen phosphate; 2-{(2,2-dimethylpropyl)[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquuiazolin-7-yl}oxy)propyl]arnino}ethyl dihydrogen phosphate; l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyI]piperidin-3-yl dihydrogen phosphate; 2-{[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJy-pyrazol-3-yl)amino]-6-metlioxyquinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; 2-[[3^{4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](3,3,3-trifIuoropropyl)amino]ethyl dihydrogen phosphate;
2- {cyclopropyl[3 -((4-[(5 - {2-[(3-fluorophenyl)amino]-2-oxoethyl} - lH-pyrazol-3-yl)amino] -6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; 2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate; {(26)-l-[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethy]}-lH-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl} methyl dihydrogen phosphate; 2-{cyclopentyl[3-({4-[(5-{2-[(3-fluorophenyl)arniao]-2-oxoe1hyl}-l/f-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJFf--pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](ethyl)amino] ethyl dihydrogen phosphate;
2-{[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]quinazoUn-7-yl}oxy)propyl]amino}-2-methylpropyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-17:r-pyrazol-3-yl)aniino]-quinazolin-7-yl}oxy)propyl](propyl)amino]ethyl dihydrogen phosphate;
{(27?)-l-[3 2-[[3-({4-[(5-{2-[(3-fluorophenyl)arru'no]-2-oxoethyl}-lff-pyrazol-3-yl)ammo]quinazolin-7-yl}oxy)propyl](2-methoxyethyl)amino]ethyl dihydrogen phosphate; and
2-{ethyl[3-({6-fluoro-4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-17?-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof.
A further preferred compound is any compound selected from: {l-[3 2-{cyclopropyl[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoemyl}-l//:-pyrazol-3-yl)arnino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate; and 2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)arnino]-6-metlioxyquinazolin-7-yl} oxy)propyl]amino}ethyl dihydrogen phosphate; 3r a pharmaceutically acceptable salt thereof.
Another preferred compound is any compound selected from: ^[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJff-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl dihydrogen phosphate; 2-{(2,2-dimethylpropyl)[3-({4-[(5-{2-[(3-fluorophenyl)amirio]-2-oxoethyl}-l^'-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]amino) ethyl dihydrogen phosphate; 2-{[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJ:r-pyrazol-3-yl)amino]-6-
methoxyquinazolin-7-yl}oxy)propyl](3333-trifluoropropyl)amino]ethyldihydrogen
phosphate;
2- {cyclopropyl[3-({4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-yl)aminoj-
6-methoxyquinazolin-7-yl}oxy)propyl]amiiio} ethyl dihydrogen phosphate; and
2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)ammo]-6-
methoxyquiBazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate;
or a pharmaceutically acceptable salt thereof.
A particularly preferred compound is any compound selected from: {(2^-!-[3-({4-[(5-{2-[(3-fluorophenyl)aniino]-2-oxoethyl}-l/r-pyrazol-3-yl)arnino> quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}metliyl dihydrogen phosphate; 2-{cyclopentyl[3-({4-[(5-{2-[(3-fluorophenyl)arnino]-2-oxoethyl}-lH-pyrazol-3-yl)arnino]-quinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH'-pyrazol-3-yl)arnino]-quinazolin-7-/!} oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate;
2-{[3-({4-[(5-{2-[(3-fluorophenyl)arrmio]-2-oxoemyl}-l//-pyrazol-3-yl)arrmao]qumazolin-7-
yl}oxy)propyl]amino}-2-methylpropyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amiiio]-quuiazolin-7-
yl}oxy)propyl](propyl)amino] ethyl dihydrogen phosphate; {(2^)-l-[3-({4-[(5-{2-[(3-fluorophenyl)arnino]-2-oxoethyl}-lH-pyrazol-3-yl)amuio]-
quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate;
3-[[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-l//--pyrazol-3-yl)arnino]-quinazolin-7-
yl}oxy)propyl](ethyl)amino]propyl dihydrogen phosphate; and
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]quinazolin-7-
yl}oxy)propyl](2-methoxyethyl)amino]ethyl dihydrogen phosphate;
or a pharmaceutically acceptable salt thereof.
An especially preferred compound of the invention is any compound selected from:
2-{cyclopentyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoemyl}-lff-pyrazol-3-yl)arnino]-
quinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)aiiuno]-2-oxoefliyl}-l£f-pyrazol-3-yl)arnino]-quinazolin-7-
^l}oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate;
I- {[3-( {4-[(5- (2-[(3 -fluorophenyl)amino]-2-oxoethyl} - lF-pyrazoI-3 -yl)amino]quinazolin-7-
^1}oxy)propyl]amino} -2-methylpropyl dihydrogen phosphate;

2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJff-pyrazol-3-yl)amino]-qiiinazolin-7-yl}oxy)propyl](propyl)amino] ethyl dihydrogen phosphate;
3-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-qiiina2;olin-7-
yl}oxy)propyl](ethyl)amino]propyl dihydrogen phosphate; and
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]quiiia2olin-7-
yl} oxy)propyl] (2-methoxyethyl)amino] ethyl dihydrogen phosphate;
or a pharmaceutically acceptable salt thereof.
A further preferred compound is any compound selected from:
2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)ainino]-6-
methoxyquinazolin-7-yl} oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate;
{(2S)-1 -[3-( (4-[(5- {2-[(3,5-difluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate;
{(2R*)-1 -[3-( {4-[(5- {2-[(3,5-difluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}niethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}4F-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](isobutyl)amino]ethyl dihydrogen phosphate; 2-[[3 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxbe%l}-lJH'-pyrazol-3-yl)ainino]-6-methoxyquiriazolin-7-yl} oxy)propyl](prop-2-yn-l-yl)amino]ethyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof.
A further preferred compound is any compound selected from: 2-[[3-( {4-[(5-{2-[(3,5-difluorophenyl)ammo]-2-oxoethyl}-l/?-pyrazol-3-yl)arnino]-6-methoxyquinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate; 2-[[3-( {4-[(5- {2-[(3,5-difluorophenyl)amino]-2-oxoethyl} -lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl] (isobutyl)amino]ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)anmo]-2-oxoethyl}-lJfir-pyrazol-3-yl)amino]-6-[nemoxyquinazolm-7-yl}oxy)propyl](propyl)arnino]ethyl dihydrogen phosphate; and ^[[3.({4-[(5-{2-[(3,5-difluorophenyl)arriino]-2-oxoe%l}-l^-pyrazol-3-yl)amino]-6-nethoxyquinazolm-7-yl}oxy)propylJ(prop-2-yn-l-yl)amino]ethyl dihydrogen phosphate; >r a pharmaceutically acceptable salt thereof.
Another more preferred compound is any compound selected from:

2-[[3
{(2J?)4-[3 i {(2J?)4-[4-({4-[(5-{2-[(23-difluorophenyl)amino]-2-oxoethyl}4H-pyrazol-3-yl)ainino]-quinazolm-7-yl) oxy)butyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; 2-[[4-({4-[(5-{2-[(2)3-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)butyl](methyl)amino]ethyl dihydrogen phosphate; and {(25)4-[4-({4-t(5-{2-[(23-dilluorophenyl)arruno]-2-oxoethyl}4H-pyrazol-3-yl)ammo^ quinazolrri-7-yl}oxy)butyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof.
A particularly preferred compound is any compound selected from: 2-[[3-({4-[(5-{2-[(2,3-difluoropheayl)arrdno]-2-oxoethyl}-lF-pyrazol-3-yl)amino]-6-methoxyqumazolin-7 -yl} oxy)propyl](propyl)amino]ethyl dihydrogen phosphate; 2-[[3 > methoxyqainazolin-7-yl} oxy)propyl](isopropyl)amino]ethyl dihydrogen phosphate; 2-[[3-( (4-[(5- {2-[(233-difluorophenyl)amrno]-2-oxoethyl} -lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](prop-2-yn-l -yl)amrno]ethyl dihydrogen phosphate;

2-[[3 Yet another preferred compound is any compound selected from: 2-[[3
2-{(cyclopropylmethyl)[3-({4-[(5-{2-[(253-difluorophenyl)amino]-2-oxoethyl}-lff-pyra2ol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof. .
Another preferred compound is any compound selected from: 2-{4-[({4-[(5-{2-[(2,3-difluorophenyl)arnino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)methyl]piperidin-l-yl}ethyl dihydrogen phosphate; 2-[[3-( {4-[(5- {2-[(2>difluorophenyl)arnino]-2-oxoethyl}- l#-pyrazol-3-yl)arnino]-quinazolm-7-yl}oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoemyl}-l//'-pyrazol-3-yl)arnino]-quinazolm-7-yl}oxy)propyl](isopropyl)amino]ethyl dihydrogen phosphate; 3-{[3-({4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoethyl}-lF-pyrazol-3-yl)amino]quinazolin-7-yl} oxy)propyljamino} -3-methylbutyl dihydrogen phosphate; 2- {(2S)-l -[3-({4-[(5- {2-[(2,3-difluorophenyl)ammo]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl} ethyl dihydrogen phosphate; {(2^)-l-[3^{4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)arnino]-quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihy±'ogen phosphate;
2-[[3-({4-[(5-{2-[(2)3-difluorophenyl)amino]-2-oxoethyl}.-l//'-pyrazol-3-yl)amino]-
quinazolin-7-yl}oxy)propyl](propyl)amino]ethyl dihydrogen phosphate;
2-[[3-( {4-[(5- {2-[(2,3-difluorophenyl)arnino]-2-pxoethyl} »l#-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)propyl](butyl)amino] ethyl dihydrogen phosphate;
2-{cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/£-pyrazol-3-
yl)amino]-quinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate; {(25)-l-[3-({4-[(5-{2-[(23-difluorophenyl)arnino]-2-oxoethyl}-l/f-pyrazol-3-yl)arnino]-
quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate;
2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lJ:f-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)butyl](propyl)amino]ethyl dihydrogen phosphate;
2-[[4-({4-[(5-{2-[(23-difluorophenyl)armno]-2-oxoethyl}-lJ!?-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)butyl](ethyl)amino]ethyl dihydrogen phosphate;
{(2^)-l-[4-({4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoethyI}-l//-pyrazol-3-yl)arnino]-
quinazolin-7-yI}oxy)butyl]pyrrolidin-2-yl}methyl dihydrogen phosphate;
2.[[4.({4-[(5-{2-[(2]3-difluorophenyl)amino]-2-oxoethyl}-lfir-pyrazol-3-
^l)aniino]quinazolin-7-yl}oxy)butyl](memyl)arnino]ethyl dihydrogen phosphate; and

- {2-[(2s3-difluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3~yl)amino]-quinazolin-7-yl}oxy)butyl]pyrrolidin-2-yl} methyl dihydrogen phosphate; or a pharmaceutically acceptable salt thereof.
Yet another preferred compound is any compound selected from: 2-[[3-({4-[(5-{2 A further particularly preferred compound is any compound selected from: {l-[3K{4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-lJ?-pyrazol-3-yl)arnino]-6-methoxyquinazolm-7-yl} oxy)propyl]piperidin-4-yl}methyl dihydrogen phosphate; {(25}-l-[3-({4-[(5-{2-[(3,5-difluorophenyl)aniino]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-6-methoxyquinazolm-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; {(2^)-l-[3
l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-ljy'-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]piperidin-3-yl dihydrogen phosphate; ((2^)-l-[3-({4-[(542-[(2^-difluorophenyl)amino]-2-oxoe%l}-l^-pyrazol-3-yl)ainiiio]-6-nethoxyquinazolin-7-yl} oxy)propyl]pyrroIidin-2-yl}methyl dihydrogen phosphate; »-{(25)-l-[3-({4-[(5-{2-[(2,3-difluorophenyO
quinazolin-7-yl) oxy)propyl]pyrrolidin-2-yl} ethyl dihydrogen phosphate; {(2^)-l-[3r a pharmaceutically acceptable salt thereof.
A nirther embodiment of the invention comprises any one of:
A^(2,3-difluorophenyl)-2- {3-[(7- {[ 1 -(2-hydroxyethyl)piperidin-4-yl]methoxy} quinazolin-4-
yl)amino]-lJc/-pyrazol-5-yl}acetamide;
A^-(2,3-difluorophenyl)-2- {3-[(7- {3-[(3-hydroxy-l, 1-
dmiethylpropyl)amuio]propoxy}quinazolin-4-yl)ammo]-U/-pyrazol-5-yl}acetamide;
A^-(2,3-difluorophenyl)-2-{3-[(7-{3-[(25)-2-(2-hydroxyethyl)pyrrolidin-l-yl]propoxy}-
quinazolin-4-yl)amino]-17:/-pyrazol-5-yl}acetamide;
JV-(2,3-difiuorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(butyl)amino]propoxy} -quinazolin-4-
yl)aminoJ-l//-pyrazol-5-yl}acetamide;
2- {3-[(7- {3-[cyclopentyl(2-hydroxyethyl)amino]propoxy} -quinazolin-4-yl)amino]-1H-
pyrazol-5-yl}-jV-(2,3-difluorophenyl)acetamide;
^-(233-difluorophenyl)-2-{3-[(7-{3-[(21S}-2-(tydroxymemy])pyrrolidin-l-yl]propoxy}-
quinazolin-4-yl)arnino]-1 fl-pyrazol-5-yl} acetamide;

N-(3 -£hiorophenyl)-2- (3 -[(7- {3-[(25}-2-(hydroxymetliyl)pyrrolidin-1 -yl]propoxy} -
quinazoIin-4-yl)amino]-lH-pyrazol-5-yl}aceta]iiide;
2-{3-[(7-{3-[cyclopentyl(2-hydroxyethyl)amino]propoxy}-quinazolin-4-yl)amino]-lH-
pyra2ol-5-yl}-A^-(3-fluorophenyl)acetamide;
7V-(3-fluorophenyl)-2- {3-[(7- {3-[ethyl(2-hydroxyethyl)amino]propoxy} -quinazolin-4-
yl)amino] - l#-pyrazol-5-yl} acetamide;
A^-(3-fluorophenyl)-2-{3-[(7-{3-[(2-hydroxy-lJ-dime1hylet3iyl)amino]propoxy}quinazolin-4-
yl)amino] -lH-pyrazol-5-yl} acetamide;
^-(3-fluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(propyl)amiao]propoxy}-quinazolin-4-
yl)amino]-lH-pyrazol-5-yl}acetamide;
JV-(3-fluorophenyl)-2-{3-[(7-{3-[(2^)-2-(hydroxymethyl)pyrrolidin-l-yl]propoxy}-
quina2olin-4-yl)aaaino]-lH-pyrazol-5-yl}acetamide;
JV"-(23-difluorophenyl)-2-{3-[(7-{4-[(2-hydroxyethyl)(propyl)ainmo]butoxy}-quinazolin-4-
yl)amino]-lff-pyrazol-5-yl}acetamide;
//-(3-fluoroplienyl)-2-{3-[(7-{4-[ethyl(2-hydroxyethyl)amino]biitoxy}-quinazolin-4-
y l)amino] -1 .ff-pyrazol-5 -yl} acetamide;
^-(2,3-difluorophenyl)-2-{3-[(7-{4-[(2^)-2-(Tiydroxymethyl)pyrrolidin-l-yl]butoxy}-
quinazolin-4-yl)amino]- lH-pyrazol-5-yl} acetamide;
JV-(23-dafluorophenyl)-2-{3-[(7-{4-[(2-hydroxyethyl)(methyl)ainino]butpxy}quijiazoliii-4-
yl)amino]- l-H-pyrazol-5 -yl} acetamide;
JV-(2,3-difluorophenyl)-2- {3-[(7- {4-[(25}-2-(hydroxymethyl)pyrrolidin-1 -yljbutoxy} -
quinazolin-4-yl)amino]- l.H-pyrazol-5-yl} acetamide;
2-{3-[(7-{3-[ethyl(3rhydroxypropyl)ainmo]propoxy}-quinazo!in-4-yl)amino]-lH~pyrazol-5-
yl}-JV-(3-iluorophenyl)acetamide;
7V-(3-fluorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyi)(2-
methoxyetiayl)amino]propoxy}quina2olin-4-yl)amino]-lfl'-pyrazol-5-yl}acetamide; and
2- {3-[(7- {3-[ethyl(2-hydroxyethyl)amino]propoxy} -6-fluoroqumazolin-4-yl)amino]-l^-
pyrazol-5-yl} -JV-(3-fluorophenyl)acetamide;
or a pharmaceutically acceptable salt thereof.
Synthetic routes to any of compounds can be found hi the examples.
A preferred compound of this embodiment is any compound selected from: W-(3-fluorophenyl)-2-{3-[(7-{3-[(21S}-2-(hydroxymethyl)pyrrolidin-l-yl]propoxy}-quinazolm4-yl)amino]-lH-pyrazol-5-yl}acetarnide;

2-{3-[(7-{3-[cyclopentyl(2-hydroxyethyl)amino]propoxy}-quinazolin^-yl)amino]-lflr-
pyrazol-5-yl}-JV"-(3-fluorophenyl)acetamide;
7V-(3-fluorophenyI)-2-{3-[(7-{3-[ethyl(2-hydroxyethyl)amiQo]propoxy}-quinazolin-4-
yl)amino]- l#-pyrazol-5-yl} acetamide;
jV-(3-fluorophenyl)-2- {3-[(7- (3-[(2-hydroxy-1,1 -dimethylethyl)ainino]propoxy} quinazolin-4-
yl)ammo]~l#-pyrazol-5-yl}acetamide;
jV-(3-fluorophenyl)-2- (3-[(7- {3-[(2-hydroxyethyl)(propyl)amino]propoxy} -quinazolin-4-
yl)amino]-lJ:f-pyrazol-5-yl}acetamide;
JV-(3-fluorophenyl)-2- {3 - [(7- {3 -[(2/?)-2-(hydroxymethyl)pyrrolidin-1 -yl]propoxy} -
quinazolin-4-yl)amino]-l//-pyrazol-5-yl} acetamide;
7vr-(3-fluorophenyl)-2- (3-[(7- {4-[ethyl(2-hydroxyethyl)amino]butoxy} -quinazolin-4-
yl)amino] -1 f/-pyrazol-5-yl} acetamide;
2- {3-[(7- {3-[ethyl(3-hydroxypropyl)amino]propoxy} -quinazolin-4-yl)amino]-lH-pyrazol-5-
yl}-A^-(3-fluorophenyl)acetamide;
A?-(3-fluorophenyl)-2- {3-[(7- (3-[(2-hydroxyethyl)(2-
methoxyethyl)amino]propoxy}quinazolin-4-yl)amino]- lH-pyrazol-5-yl}acetamide; and
2-{3-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}-6-fluoroquinazolin-4-yl)amino]-l/f-
pyrazol-5-yl) -^-(S-fluoropheny^acetamide;
sr a pharmaceutically acceptable salt thereof.
Another preferred compound is any compound selected from :
A^-(23-difluorophenyl)-2-{3-[(7-{[l-(2-hydroxyethyl)piperidui-4-yl]methoxy}quinazolin-4-yl)amino]-l#-pyrazol-5-yl} acetamide; AH2,3-difluorophenyl)-2- {3-[(7- {3-[(3-hydroxy-1,1 -
dimethylpropyl)amino]propoxy} quinazolin-4-yl)amino]- UZ-pyrazol-5-yl} acetamide; A^(2,3-difluorophenyl)-2-{3-[(7-{3-[(26)-2-(2-hydroxyethyl)pyrrolidin-l-yl]propoxy}-quinazolin-4-yl)amino]-l^"-pyrazol-5-yl}acetamide;
Ar-(2,3-difluorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(butyl)amino]propoxy} -quinazolin-4-yl)arnino]-1 JY-pyrazol-5-yl} acetamide;
2-{3-[(7-{3-[cyclopentyl(2-hydroxyemyl)ammo]propoxy}-quinazolin-4-yl)amiiio]-lH-pyrazol-5-yl}-jV-(2,3-difluorophenyl)acetamide;
/V-(2,3-difluorophenyl)-2-{3-[(7-{3-[(26)-2-(hydroxymethyl)pyrrolidin-l-yl]propoxy}-quinazolin-4-yl)amino]-lJfir-pyrazol-5-yl}acetamide;

A^-(23-difluorophenyl)-2-{3-[(7-{4-[(2-hydroxyethyl)(propyl)amino]butoxy}-quinazolin-4-
yl)amino] - l.fl-pyrazol-5 -yl} acetamide;
^-(2,3-difluorophenyl)-2-{3-[(7-{4-[(2^)-2-(hydroxymethyl)pyrrolidin-l-yl]butoxy}-
quinazolin-4-yl)amino]-lH-pyrazol-5-yl} acetamide;
JV-(2^-difluorophenyl)-2-{3-[(7-{4-[(2-hydroxyeiiiyl)(methyl)amino]butoxy}qumazolin-4-
yl)amino]-l#-pyrazol-5-yl} acetamide; and
AH2,3-difluorophenyl)-2- {3-[(7- {4-[(21S)-2-(hydroxymethyl)pyrrolidin-1 -yl]butoxy} -
quinazolin-4-yl)amino]-lJff-pyrazol-5-yl} acetamide;
or a pharmaceutically acceptable salt thereof.
In another aspect the present invention provides a process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof, which process comprises converting a compound of formula (II) into a compound of formula (I) by phosphorylation of an appropriate hydroxy group:

(Formula Remove)
where A, X, m, R3, R4, R5, R6, R7 and R9 are as defined for formula (I); and Z' is a group selected from —NR1 R2, hydroxy, Ca-ecycloalkyl which Cs-gcycloalkyl is substituted by hydroxy or Ci^alkyl substituted by hydroxy, and a 4- to 7-membered ring linked via a carbon atom containing a nitrogen atom and optionally containing a further nitrogen atom, which ring may be saturated, unsaturated or partially saturated wherein the ring is substituted on carbon or nitrogen by hydroxy or Chalky! substituted by hydroxy and wherein the ring is optionally further substituted on carbon or nitrogen by 1,2 or 3 halo or Chalky! groups; R1' is a group selected from -COR8', -CONR8>R9 and Chalky! which Chalky! is substituted by hydroxy and optionally further substituted by 1 or 2 halo or methoxy groups; R2' is a group selected from hydrogen, -COR10, -CONR^R1' and Cj.6alkyl which C].6alkyl is optionally substituted by 1,2 or 3 halo or C^alkoxy groups or -S(0)pRn (where p is 0, 1 or 2) or hydroxy, or R2 is selected from C2-6alkenyl, C2.6alkynyl5 C3.6cycloalkyl and Cs-gcycloalkylCj^alkyl;

or R1 and R2 together with the nitrogen to which they are attached form a 4- to 7- membered
ring optionally containing a further nitrogen atom which may be saturated, unsaturated or
partially saturated wherein the ring is substituted on carbon or nitrogen by a group selected
from hydroxy and Chalky! substituted by hydroxy or -NR8>R9 and where the ring is
optionally further substituted on carbon or nitrogen by 1, 2 or 3 halo or Chalky! groups; and
where R8 is Chalky! substituted by hydroxy and optionally further substituted by 1 or 2 halo
or methoxy groups:
and thereafter if necessary:
i) converting a compound of the formula (I) into another compound of the formula (I); and/or
ii) removing any protecting groups; and/or
iii) forming a pharmaceutically acceptable salt thereof.
Phosphorylation may be suitably performed by treatment with 1-H tetrazole (or a suitable replacement such as S-ethyl tetrazole or pyridinium hydrochloride) and di-tert-butyldiemylphosphoramidite or dibenzyldiethylphosphoramidite at 5 to 35 °C under an inert atmosphere for 30 minutes to 4 hours followed by treatment with an oxidizing agent such as rneta-chloroperbenzoic acid (mCPBA) or 30% aqueous hydrogen peroxide at -10 to 25 °C for 2 to 18 hour. Deprotection of the tert-butyl groups to yield the phosphate group is required as a. final step with these reagents and may be readily achieved by treatment with 4.0 N lydrochloric acid in 1,4-dioxane at 10 to 35 °C for 12 to 18 hours.
This process may further comprise a method for the preparation of a compound of K>rmula (II) where Z' is -NR1 R2 which method comprises the reaction of a compound of brmula (III) where L is a leaving group such as halo (e.g.chloro): (Formula Remove)
-34-Rr
R2'
formula (IV).
Suitable reaction conditions for this method include heating a compound of formula (ID) with an excess of amine of formula (IV) in an inert solvent such as dimethylacetamide, with or without the addition of a suitable catalyst (such as te/ra-n-butylammoniuim iodide or potassium iodide) at a temperature of 50 to 100 °C for 12 to 72 hours. In an alternative procedure., the leaving group L in formula (III) may be a carboxaldehyde and the reaction with amine (IV) may be carried out under reductive conditions using a reducing agent such as sodium cyanoborohydride.
The amines of formula (IV) are known in the art or may be prepared by the skilled person using methods known in the art.
The process may further comprise a method for the preparation of a compound of formula (III) where X is NR14 which method comprises the reaction of a compound of formula (V) where R' and R" are alkyl groups such as methyl and ethyl and L is as defined in relation to formula (III):
(Formula Remove)
with a compound of formula (VI) where R may be either hydrogen or a group such as tert-butoxycarbonyl (Boc) or trityl:
(Formula Remove)
Such a reaction can be achieved under a range of conditions described in the literature, such as heating a compound of formula (V) with a compound of formula (VI) in a solvent such as acetic acid at a temperature of 100 to 130 °C for 2 to 18 hours.
Alternatively, the process may further comprise a method for Hie preparation of a compound of formula (HI) where X is NR14, O or S which method comprises the reaction of a compound of formula (VII) where R* is a leaving group such as halo (e.g.chloro):
(Formula Remove)



with a compound of formula (VI) where R is either hydrogen or tert-butoxycarbonyl (Boc) or trityl. Such a reaction can be achieved under a range of conditions described in the literature, such as heating a compound of formula (VII) with a compound of formula (VI) in a solvent such as isopropanol or dimethylacetamide, in the presence of an acid catalyst such as hydrochloric acid, at a temperature of 80 to 100 °C for 2 to 6 hours. Alternatively the reaction may be effected using a base such as sodium hydride' carrying out the reaction in an inert solvent such as dimethylformamide at a temperature of 50 to 80 °C for 2 to 6 hours.
Compounds of formula (V) can be prepared from a compound of formula (VET) where P is a hydroxy protecting group such as benzyl:

(Formula Remove)
by reaction with a compound of formula (IX) where L' is a leaving group such as halo (e.g. bromo) and L is as defined in relation to formula (III):

L'
formula (DC)
Such a reaction can be achieved (after removal of the protecting group using a method selected from those already described in the literature) under a range of conditions described in the literature such as heating a compound of formula (VIII) with a compound of formula (IX) in the presence of a catalyst such as caesium carbonate in a solvent such as acetonitrile at a temperature of 80 to 100 °C for 1 to 4 hours.
A method for the preparation of a compound of formula (VHT) comprises the reaction compound of formula (X) where P is as defined in relation for formula (VIE):
(Formula Remove)
with an appropriate acetal such as TV.N-dimernylformamide dimethyl acetal. The reaction is suitably effected in an organic solvent such as toluene or benzene, at elevated temperature, conveniently at the reflux temperature of the solvent.
Compounds of formula (X) are either known compounds or they can be prepared by the skilled person using conventional methods. In particular, compounds of formula (X) may be prepared by reduction of the corresponding nitro compound of formula (XI) where P is as described in relation to formula (VIII):
(Formula Remove)
Suitable reaction conditions are illustrated hereinafter.
Compounds of formula (XI) may be obtained by nitration of a compound of formula (XII) where P is as defined in relation to formula (VIE)
(Formula Remove)
for example, using nitric acid as the nitrating agent. Again, suitable reaction conditions are illustrated hereinafter.
The nitrile of formula (XII) may be derived by reaction of the corresponding aldehyde of formula (XIII) with hydroxylamine as illustrated hereinafter:
£(Formula Remove)
The process may further comprise a method for the preparation of a compound according to formula (VII) which method comprises the reaction of a compound of formula
(Formula Remove)
where L* is a hydroxy group, with a suitable chlorinating agent such as thionyl chloride, phoshoryl chloride or phoshorus pentachloride. Again, suitable reaction conditions are illustrated hereinafter.
Compounds of formula (XIV) are either known compounds or they can be prepared by the skilled person using conventional methods. In particular, compounds of formula (XIV) may be prepared by reaction of a compound of formula (XV) where L" is a leaving group such as halo (fluoro)

(Formula Remove)
compound of formula (XVI) where L* is a hydroxy group:
formula (XVI) Suitable reaction conditions are illustrated hereinafter.
Compounds of formula (XV) are either known compounds or they can be prepared by the skilled person using conventional methods. In particular, compounds of formula (XV) may be prepared by reaction of a compound of formula (XVTI) (where L" is a leaving group 1 0 such as halo (fluoro) and L" ' is an alkoxy or hydroxy group) by reaction with neat formamide at a temperature of 140 to 200 °C for 3 to 6 hours. (Formula Remove)
Suitable reaction conditions are illustrated hereinafter.
15 Compounds of formula (XVII) are either known compounds or they can be prepared
by the skilled person using conventional methods. In particular, compounds of formula (XVII) may be prepared by reduction of a compound of formula (XVIII) (where L" is a leaving group such as halo (fluoro) and L'" is an alkoxy or hydroxy group) using a reducing agent such as sodium dithionite in a water: dichloromethane solvent system at ambient
20 temperature for 1 to 3 hours.


(Formula Remove)
formula (XVffl)
Compounds of formula (XVIII) may be obtained by nitration of a compound of formula (XIX) where L" and L"' are as defined in relation to formula (XVIII)
L'"

R3
(Formula Remove)
for example, using nitric acid as the nitrating agent. Again, suitable reaction conditions are illustrated hereinafter.
The process may further comprise a method for the preparation of a compound according to formula (VI) where X is NR14, 0 or S which method comprises the reaction, of a compound of formula (XX), where P is a suitable protecting group:
(Formula Remove)
formula (XX)
5
with an amine of formula HNR R in the presence of a coupling reagent (such as 0-(7-azabenzotriazol- 1 -yl)-N,N,N ', N -tetramethyluronium hexafluorophosphate) and diisopropylethylamine in a solvent (such as dimethylacetamide) under inert and anhydrous conditions.
A compound of formula (XX) where X is NR14 and P is COOR may be prepared from a compound of formula (XXI):
(Formula Remove)
with a compound of formula (XXII) where L is an appropriate leaving group:
Suitable reagent and reaction conditions for this reaction include the use of di(/e/-?-butyl)dicarbonate and triethylamine in tetrahydroftiran at 0 °C under a nitrogen atmosphere.
A compound of formula (III) may also be prepared (following deprotection) from a compound of formula (XX) by reacting it with a compound of formula (V) under a range of conditions described in the literature., such as heating the reaction mixture in a solvent such as acetic acid at a temperature of 1 00 to 130°C for 2 to 18 hours. The product, a compound of formula (XXIII):
(Formula Remove)
may men be reacted with an amine of formula HNR4R5 in the presence of a coupling agent (such as O-(7-azabenzotriazol-l-yl)-7V;7V>7V>,JV -tetramethyluroniurn hexafluorophosphate) and diisopropylethylamine in a solvent (such as dimethylacetamide) under inert and anhydrous conditions.
Further a compound of formula (XXIII) may also be prepared by reacting a deprotected compound of formula (XX) with a compound of formula (VII) under a range of conditions described in the literature, such as heating the reaction mixture in a solvent such as isopropanol or dimethylacetamide, in the presence of an acid catalyst such as hydrochloric

~v.^, ui. a icuijjcracure oi su to 100 UC for 2 to 6 hours. Alternatively the reaction may be effected using a base such as sodium hydride; carrying out the reaction in an inert solvent such as dimethylformamide at a temperature of 50 to 80 °C for 2 to 6 hours.
Compounds of formula (XXI) which comprise a heteraromatic ring are made according to the literature. However for illustrative purpose, when A is a pyrazole ring, a compound of formula (XXI) may be prepared according to the following scheme:
(Formula Remove)
It will be appreciated that certain of the various ring substituents in the compounds of the present invention may be introduced by standard aromatic substitution reactions or generated by conventional functional group modifications either prior to or immediately following the processes mentioned above, and as such are included in the process aspect of the invention. Such reactions and modifications include, for example, introduction of a substiruent by means of an aromatic substitution reaction, reduction of substituents, alkylation of substituents and oxidation of substituents. The reagents and reaction conditions for such procedures are well known in the chemical art. Particular examples of aromatic substitution reactions include the introduction of a nitro group using concentrated nitric acid, the introduction of an acyl group using, for example, an acyl halide and Lewis acid (such as aluminium trichloride) under Friedel Crafts conditions; the introduction of an alkyl group using an alkyl halide and Lewis acid (such as aluminium trichloride) under Friedel Crafts conditions; and the introduction of a halogen group. Particular examples of modifications include the reduction of a nitro group to an amino group by for example, catalytic hydrogenation with a nickel catalyst or treatment with iron in the presence of hydrochloric acid with heating; oxidation of alkylthio to alkylsulphinyl or alkyl sulphonyl.
It will also be appreciated that in some of the reactions mentioned herein it may be necessary/desirable to protect any sensitive groups in the compounds. The instances where protection is necessary or desirable and suitable methods for protection are known to those skilled in the art. Conventional protecting groups may be used in accordance with standard practice (for illustration see T.W. Green, Protective Groups in Organic Synthesis, John Wiley and Sons, 1991). Thus, if reactants include groups such as amino, carboxy or hydroxy it may be desirable to protect the group in some of the reactions mentioned herein.

protecting group for an amino or alkylamino group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an alkoxycarbonyl group, for example a methoxycarbonyl, ethoxycarbonyl or ter/-butoxycarbonyl group, an aryhnethoxycarbonyl group, for example benzyloxycarbonyl, or an aroyl group, for example benzoyl. The deprotection conditions for the above protecting groups necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or alkoxycarbonyl group or an aroyl group may be removed for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively an acyl group such as a /er/'-butoxycarbonyl group may be removed, for example., by treatment with a suitable acid as hydrochloric, sulphuric or phosphoric acid or trifluoroacetic acid and an arylmethoxycarbonyl group such as a benzyloxycarbonyl group maybe removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon, or by treatment with a Lewis acid for example boron tris(trifluoroacetate). A suitable alternative protecting group for a primary amino group is, for example, a phthaloyl group which may be removed by treatment with an alkylamine, for example dimethylaniinopropylamirie, or with hydrazine. A suitable protecting group for a hydroxy group is, for example, an acyl group, fo* example an alkanoyl group such as acetyl, an aroyl group, for example benzoyl, or an arylmethyl group, for example benzyl. The deprotection conditions for the above protecting groups will necessarily vary with the choice of protecting group. Thus, for example, an ^cyl group such as an alkanoyl or an aroyl group may be removed, for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide-Alternatively an arylmethyl group such as a benzyl group may be removed, for example, "by hydrogenation over a catalyst such as palladium-on-carbon.
A suitable protecting group for a carboxy group is, for example, an esterifying group, for example a methyl or an ethyl group which may be removed, for example, by hydrolysis with a base such as sodium hydroxide, or for example a tert-bntyl group which may be removed, for example, by treatment with an acid, for example an organic acid such as trifluoroacetic acid, or for example a benzyl group which may be removed, for example, t>y hydrogenation over a catalyst such as palladium-on-carbon.
The protecting groups may be removed at any convenient stage in the synthesis conventional techniques well known in the chemical art.

According to a farther aspect of the invention there is provided a pharmaceutical composition which comprises a compound formula (I), or a pharmaceutically acceptable salt thereof, as defined herein in association with a pharmaceutically acceptable diluent or carrier. The compositions of the invention may be in a form suitable for oral use (for example as tablets, lozenges, hard or soft capsules, aqueous or oily suspensions, emulsions, dispersible powders or granules, syrups or elixirs), for topical use (for example as creams, ointments, gels, or aqueous or oily solutions or suspensions), for administration by inhalation (for example as a finely divided powder or a liquid aerosol), for administration by insufflation (for example as a finely divided powder) or for parenteral administration (for example as a sterile aqueous or oily solution for intravenous, subcutaneous, intramuscular or intramuscular dosing or as a suppository for rectal dosing).
The compositions of the invention may be obtained by conventional procedures using conventional pharmaceutical excipients, well known in the art. Thus, compositions intended for oral use may contain, for example, one or more colouring, sweetening, flavouring and/or preservative agents.
Suitable pharmaceutically acceptable excipients for a tablet formulation include, for example, inert diluents such as lactose, sodium carbonate, calcium phosphate or calcium carbonate, granulating and disintegrating agents such as corn starch or algenic acid; binding agents such as starch; lubricating agents such as magnesium stearate, stearic acid or talc; preservative agents such as ethyl or propyl j>hydroxybenzoate, and anti-oxidants, such as ascorbic acid. Tablet formulations may be uncoated or coated either to modify their disintegration and the subsequent absorption of the active ingredient within the gastrointestinal track, or to improve their stability and/or appearance, in either case, using conventional coating agents and procedures well known in the art.
Compositions for oral use may be in the form of hard gelatin capsules in which the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules in which the active ingredient is mixed with water or an oil such as peanut oil, liquid paraffin, soya bean oil, coconut oil, or preferably olive oil, or any other acceptable vehicle.
Aqueous suspensions generally contain the active ingredient in finely powdered form together with one or more suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylrnethylcellulose, sodium alginate, polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents such as lecithin or condensation

products of an alkylene oxide with fatty acids (for example polyoxyethylene stearate), or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives (such as ethyl or propyl p_-hydroxybenzoate, anti-oxidants (such as ascorbic acid), colouring agents, flavouring agents, and/or sweetening agents (such as sucrose, saccharine or aspartame).
Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil (such as arachis oil, olive oil, sesame oil or coconut oil) or in a mineral oil (such as liquid paraffin). The oily suspensions may also contain a thickening agent such as beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set out above, and flavouring agents may be added to provide a palatable oral preparation. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.
Dispersible or lyophilised powders and granules suitable for preparation of an aqueous suspension or solution by the addition of water generally contain the active ingredient together with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients such as sweetening, flavouring and colouring agents, may also be present.
The pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, such as olive oil or arachis oil, or a mineral oil, such as for example liquid paraffin or a mixture of any of these. Suitable emulsifying agents may be, for example, naturally-occurring gums such as gum acacia or gum tragacanth, naturally-occurring phosphatides such as soya bean, lecithin, an esters or partial esters derived from fatty acids and hexitol anhydrides (for example sorbitan monooleate) and condensation products of the said partial esters with ethylene oxide such as polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening, flavouring and preservative agents.

Syrups and elixirs may be formulated with sweetening agents such as glycerol, propylene glycol, sorbitol, aspartame or sucrose, and may also contain a demulcent, preservative, flavouring and/or colouring agent.
The pharmaceutical compositions may also be in the form of a sterile injectable aqueous or oily suspension, solutions, emulsions or particular systems, which may be formulated according to known procedures using one or more of the appropriate dispersing or wetting agents and suspending agents, which have been mentioned above. A sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example a solution in polyethylene glycol.
Suppository formulations may be prepared by mixing the active ingredient with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Suitable excipients include, for example, cocoa butter and polyethylene glycols.
Topical formulations, such as creams, ointments, gels and aqueous or oily solutions or suspensions, may generally be obtained by formulating an active ingredient with a conventional, topically acceptable, vehicle or diluent using conventional procedure well known in the art.
Compositions for administration by insufflation may be in the form of a finely divided powder containing particles of average diameter of, for example, SOfim or much less preferably 5 urn or less and more preferably between 5|im and l|jni, the powder itself comprising either active ingredient alone or diluted with one or more physiologically acceptable carriers such as lactose. The powder for insufflation is then conveniently retained in a capsule containing, for example, 1 to 50mg of active ingredient for use with a turbo-inhaler device, such as is used for insufflation of the known agent sodium cromoglycate.
Compositions for administration by inhalation may be in the form of a conventional pressurised aerosol arranged to dispense the active ingredient either as an aerosol containing finely divided solid or liquid droplets. Conventional aerosol propellants such as volatile fluorinated hydrocarbons or hydrocarbons may be used and the aerosol device is conveniently arranged to dispense a metered quantity of active ingredient.
For further information on formulation the reader is referred to Chapter 25.2 in Volume 5 of Comprehensive Medicinal Chemistry (Corwin Hansch; Chairman of Editorial Board), Pergamon Press 1990.

Therefore in a further aspect of the invention there is provided a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in therapy. Further provided is a compound of formula (I), or a pliarmaceutically acceptable salt thereof, for use as a medicament. A compound of formula (I), or a pharmaceutically acceptable salt thereof, is also provided for use in the treatment of a disease where the inhibition of one or more Aurora kinase is beneficial. In particular it is envisaged that inhibition of Aurora-A kinase and/or Aurora-B kinase may be beneficial. Preferably inhibition of Aurora-B kinase is beneficial. A compound of formula (I), or a pharmaceutically acceptable salt thereof, has further use in the treatment of hyperproliferative diseases such as cancer and in particular colorectal, breast, lung, prostate, pancreatic or bladder and renal cancer or leukemias or lymphomas.
Additionally a compound of formula (I), or a pharmaceutically acceptable salt thereof is provided for use in a method of treatment of a warm-blooded animal such as man by therapy. According to this aspect, there is provided a compound of formula (I) or a pharmaceutically acceptable salt thereof for use in the method of treating a human suffering from a disease in which the inhibition of one or more Aurora kinases is beneficial, comprising the steps of administering to a person in need thereof a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof. In particular it is envisaged that inhibition of Aurora-A kinase and/or Aurora-B kinase may be beneficial. Preferably inhibition of Aurora-B kinase is beneficial. Further provided is a compound of formula (I) or a pharmaceutically acceptable salt thereof for use in the method of treating a human suffering from a hyperproliferative disease such as cancer and in particular particular colorectal, breast, lung, prostate, pancreatic or bladder and renal cancer or leukemias or lymphomas, comprising the steps of administering to a person hi need thereof a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.
In another aspect of the invention, there is provided the use of a compound of formula (I) or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for the treatment of a disease where the inhibition of one or more Aurora kinase is beneficial. In particular it is envisaged that inhibition of Aurora-A kinase and/or Aurora-B kinase may be beneficial. Preferably inhibition of Aurora-B kinase is beneficial. In another aspect of the invention, there is provided the use of a compound of formula (I) or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for the treatment of hyperproliferative diseases such as cancer and in particular colorectal, breast, lung, prostate,

pancreatic or bladder and renal cancer or leukemias or lymphomas.
For the above mentioned therapeutic uses the dose administered will vary with the compound employed, the mode of administration, the treatment desired, the disorder indicated and the age and sex of the animal or patient. The size of the dose would thus be calculated according to well known principles of medicine.
In using a compound of formula (I) for therapeutic or prophylactic purposes it will generally be administered so that a daily dose in the range, for example, 0.05 nag/kg to 50 mg/kg body weight is received, given if required in divided doses. In general lower doses will be administered when a parenteral route is employed. Thus, for example, for intravenous administration, a dose in the range, for example, 0.05 mg/kg to 25 mg/kg body weight will generally be used. Similarly, for administration'by inhalation, a dose in the range, for example, 0.05 mg/kg to 25 mg/kg body weight will be used.
The treatment defined hereinbefore may be applied as a sole therapy or may involve, in addition to the compound of the invention, conventional surgery or radiotherapy or chemotherapy. Such chemotherapy may include one or more of the following categories of anti-tumour agents :-
(i) antiproliferative/antineoplastic drugs and combinations thereof, as used in medical oncology, such as alkylating agents (for example cis-platin, carboplatin, cyclophosphamide, nitrogen mustard, melphalan, chlorambucil, busulphan and nitrosoureas); antimetabolites (for example antifolates such as fluoropyrimidines like 5-fluorouracil and tegafur, raltitrexed, rnethotrexate, cytosine arabinoside and hydroxyurea; antitumour antibiotics (for example anthracyclines like adriamycin, bleomycin, doxorubicin, daunomycin, epirubicin, idarubicin, mitomycin-C, dactinomycin and mithramycin); antimitotic agents (for example vinca alkaloids like vincristine, vinblastine, vindesine and vinorelbine and taxoids like taxol and taxotere); and topoisomerase inhibitors (for example epipodophyllotoxins like etoposide and teniposide, amsacrine, topotecan and camptothecin);
(ii) cytostatic agents such as antioestrogens (for example tamoxifen, toremifene, raloxifene, droloxifene and iodoxyfene), antiandrogens (for example bicalutamide, flutamide, nilutamide and cyproterone acetate), LHRH antagonists or LHRH agonists (for example goserelin, leuprorelin and buserelin), progestogens (for example megestrol acetate), aromatase inhibitors (for example as anastrozole, letrozole, vorazole and exemestane) and inhibitors of Sa-reductase such as finasteride;

(iii) agents which inhibit cancer cell invasion (for example metalloproteinase inhibitors like marimastat and inhibitors of urokinase plasminogen activator receptor function); (iv) inhibitors of growth factor function, for example such inhibitors include growth factor antibodies, growth factor receptor antibodies (for example the anti-erbb2 antibody
i trastuzumab [Herceptin™] and the anti-erbbl antibody cetuximab [C225]), farnesyl transferase inhibitors, tyrosine kinase inhibitors and serine-threonine kinase inhibitors, for example inhibitors of the epidermal growth factor family (for example EGFR family tyrosine kinase inhibitors such as JV-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-morpholiBopropoxy)quinazolin-4-amine (gefitinib, AZD1839), ^-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine (erlotinib, OSI-774) and 6-acrylamido-JV-(3-chloro-4-fluorophenyl)-7-(3-morpholinopropoxy)quinazolin-4-amine (CI 1033)), for example inhibitors of the platelet-derived growth factor family and for example inhibitors of the hepatocyte growth factor family;
(v) antiangiogenic agents such as those which inhibit the effects of vascular endothelial growth factor, (for example the anti-vascular endothelial cell growth factor antibody bevacizumab [Avastin™], compounds such as those disclosed in Internationa] Patent Applications WO 97/22596, WO 97/30035, WO 97/32856 and WO 98/13354) and compounds that work by other mechanisms (for example linomide, inhibitors of integrin ocvpS function and angiostatin);
(vi) vascular damaging agents such as Combretastatin A4 and compounds disclosed in International Patent Applications WO 99/02166, WOOO/40529, WO 00/41669, W001/92224, WO02/04434 and WO02/08213;
(vii) antisense therapies, for example those which are directed to the targets listed above, such as ISIS 2503, an anti-ras antisense;
(viii) gene therapy approaches, including for example approaches to replace aberrant genes such as aberrant p53 or aberrant BRCA1 or BRCA2, GDEPT (gene-directed enzyme pro-drug therapy) approaches such as those using cytosine deaminase, thymidine kinase or a bacterial nitroreductase enzyme and approaches to increase patient tolerance to chemotherapy or radiotherapy such as multi-drug resistance gene therapy; and
(ix) immunotherapy approaches, including for example ex vivo and in vivo approaches to increase the immunogenicity of patient tumour cells, such as transfection with cytokines such as interleukin 2, interleukin 4 or granulocyte-macrophage colony stimulating factor,
approaches to decrease T-cell anergy, approaches using transfected immune cells such as

cytokine-transfected dendritic cells, approaches using cytokine-transfected tumour cell lines and approaches using anti-idiotypic antibodies.
In addition a compound of the invention may be used in combination with one or more cell cycle inhibitors. In particular with cell cycle inhibitors which inhibit bubl, bubRl or CDK. Such conjoint treatment may be achieved by way of the simultaneous, sequential or separate dosing of the individual components of the treatment. Such combination products employ the compounds of this invention within the dosage range described hereinbefore and the other pharmaceutically active agent within its approved dosage range.
In addition to their use in therapeutic medicine, the compounds of formula (I) and their pharmaceutically acceptable salts are also useful as pharmacological tools in the development and standardisation of in vitro and in vivo test systems for the evaluation of the effects of inhibitors of cell cycle activity in laboratory animals such as cats, dogs, rabbits, monkeys, rats and mice, as part of the search for new therapeutic agents.
In the above other pharmaceutical composition, process, method, use and medicament manufacture features, the alternative and preferred embodiments of the compounds of tie invention described herein also apply.
The compounds of the invention inhibit the serine-threonine kinase activity of the Aurora kinases, in particular Aurora-A and/or Aurora-B and thus inhibit the cell cycle aid cell proliferation. These properties may be assessed for example, using one or more of the procedures set out below. Whilst not wishing to be bound by theoretical constraints, it is believed that the compounds of formula (I) described herein may act as prodrugs. In procedures (c) and (d) set out below it is believed that a phosphonooxy group present in he compound of formula (I) is cleaved in situ to yield a hydroxy group and that such cleavaje is necessary for activity is these assays, (a) In Vitro Aurora-A kinase inhibition test
This assay determines the ability of a test compound to inhibit serine-threonine kiase activity. DNA encoding Aurora-A may be obtained by total gene synthesis or by cloning.rhis DNA may then be expressed in a suitable expression system to obtain polypeptide with serine-threonine kinase activity, hi the case of Aurora-A, the coding sequence was isolate! from cDNA by polymerase chain reaction (PCR) and cloned into the BamHl and Notl restriction endonuclease sites of the baculovirus expression vector pFastBac HTc (GibcoBRL/Life technologies). The 5' PCR primer contained a recognition sequence for tb restriction endonuclease BamHl 5' to the Aurora-A coding sequence. This allowed the

insertion of the Aurora-A gene in frame with the 6 histidine residues, spacer region and rTEV protease cleavage site encoded by the pFastBac HTc vector. The 3' PCR primer replaced the Aurora-A stop codon with additional coding sequence followed by a stop codon and a recognition sequence for the restriction endonuclease Notl. This additional coding sequence (5' TAG CCA TAG GAT GTT CCA GAT TAG GCT TCT TAA 3') encoded for the polypeptide sequence YPYDVPDYAS. This sequence, derived from the influenza hemagglutin protein, is frequently used as a tag epitope sequence that can be identified using specific monoclonal antibodies. The recombinant pFastBac vector therefore encoded for an N-terrninally 6 bis tagged, C terminally influenza hemagglutin epitope tagged Aurora-A protein. Details of the methods for the assembly of recombinant DNA molecules can be found in standard texts, for example Sambrook et al. 1989, Molecular Cloning - A Laboratory Manual, 2nd Edition, Cold Spring Harbor Laboratory press and Ausubel et al. 1999, Current Protocols in Molecular Biology, John Wiley and Sons hie.
Production of recombinant virus can be performed following manufacturer's protocol from GibcoBRL. Briefly, the pFastBac-1 vector carrying the Aurora-A gene was transformed into E. coli DHlOBac cells containing the baculovirus genome (bacmid DNA) and via a transposition event in the cells, a region of the pFastBac vector containing gentamycin resistance gene and the Aurora-A gene including the baculovirus polyhedrin promoter was transposed directly into the bacmid DNA. By selection on gentamycin, kanamycin, tetracycline and X-gal, resultant white colonies should contain recombinant bacmid DNA encoding Aurora-A. Bacmid DNA was extracted from a small scale culture of several BHIOBac white colonies and transfected into Spodoptera frugiperda S£21 cells grown in TCI00 medium (GibcoBRL) containing 10% serum using CellFECTIN reagent (GibcoBRL) following manufacturer's instructions. Virus particles were harvested by collecting cell culture medium 72 hrs post transfection. 0.5 mis of medium was used to infect 100 ml suspension culture of S£21 s containing 1 x 107 cells/ml. Cell culture medium was harvested 48 hrs post infection and virus titre determined using a standard plaque assay procedure. Virus stocks were used to infect Sf9 and "High 5" cells at a multiplicity of infection (MOI) of 3 to ascertain expression of recombinant Aurora-A protein.
For the large scale expression of Aurora-A kinase activity, Sf21 insect cells were grown at 28°C in TCI 00 medium supplemented with 10% foetal calf serum (Viralex) and 0.2% F68 Pluronic (Sigma) on a Wheaton roller rig at 3 r.p.m. When the cell density reached 1.2xl06 cells ml"1 they were infected with plaque-pure Aurora-A recombinant virus at a

multiplicity of infection of 1 and harvested 48 hours later. All subsequent purification steps were performed at 4°C. Frozen insect cell pellets containing a total of 2.0 x 108 cells were thawed and diluted with lysis buffer (25 mM HEPES (N-[2-hydroxyethyl]piperazine-N'-[2-ethanesulphonic acid]) pH7.4 at 4°C, 100 mM KC1,25 mM NaF, 1 mM Na3VO4, 1 mM PMSF (phenyknethylsulphonyl fluoride), 2 mM 2-mercaptoethanol, 2 mM imidazole, 1 ug/ml aprotinin, 1 ug/ml pepstatin, 1 pg/ml leupeptin), using 1.0 ml per 3 x 107 cells. Lysis was achieved using a dounce homogeniser, following which the lysate was centrifuged at 41,000^ for 35 minutes. Aspirated supernatant was pumped onto a 5 mm diameter chromatography column containing 500 pi Ni NTA (nitrilo-tri-acetic acid) agarose (Qiagen, product no. 30250) which had been equilibrated in lysis buffer. A baseline level of UV absorbance for the eluent was reached after washing the column with 12 ml of lysis buffer followed by 7 ml of wash buffer (25 mM HEPES pH7.4 at 4°C , 100 mM KC1,20 mM imidazole, 2 mM 2-mercaptoethanol). Bound Aurora-A protein was eluted from the column using elution buffer (25 mM HEPES pH7.4 at 4°C , 100 mM KC1, 400 mM imidazole, 2 mM 2-mercaptoethanol). An elution fraction (2.5 ml) corresponding to the peak in UV absorbance was collected. The elution fraction, containing active Aurora-A kinase, was dialysed exhaustively against dialysis buffer (25 mM HEPES pH7.4 at 4°C , 45% glycerol (v/v), 100 mM KC1, 0.25% Nonidet P40 (v/v), 1 mM dithiothreitol).
Each new batch of Aurora-A enzyme was titrated in the assay by dilution with enzyme diluent (25mM Tris-HCl pH7.5, 12.5mM KC1, 0.6mM DTT). For a typical batch, stock enzyme is diluted 1 in 666 with enzyme diluent and 20ul of dilute enzyme is used for each assay well. Test compounds (at lOmM in dimethylsulphoxide (DMSO) were diluted with water and lOfil of diluted compound was transferred to wells in the assay plates. "Total" and "blank" control wells contained 2.5% DMSO instead of compound. Twenty microlitres of freshly diluted enzyme was added to all wells, apart from "blank" wells. Twenty microlitres of enzyme diluent was added to "blank" wells. Twenty microlitres of reaction mix (25 mM Tris-HCl, 78.4 mM KC1, 2.5 mM NaF, 0.6 mM dithiothreitol, 6.25 mM MnCl2, 6.25 mM ATP, 7.5 uM peptide substrate [biotin-LRRWSLGLRRWSLGLRRWSLGLRRWSLG]) containing 0.2 \id ['y33P]ATP (Amersham Pharmacia, specific activity >2500 Ci/mmol) was then added to all test wells to start the reaction. The plates were incubated at room temperature for 60 minutes. To stop the reaction 100 jil 20% v/v orthophosphoric acid was added to all wells. The peptide substrate was captured on positively-charged nitrocellulose P30 filtermat (Whatman) using a 96-well plate harvester (TomTek) and then assayed for

incorporation of 33P with a Beta plate counter. "Blank" (no enzyme) and "total" (no compound) control values were used to determine the dilution range of test compound which gave 50% inhibition of enzyme activity.
In this test, the compounds of the invention give 50% inhibition of enzyme activity at concentrations of 0.3 nM to 1000 nM and in particular compound 5 in Table 1 gave 50% inhibition of enzyme activity at a concentration of 5.5 nM.
(b) In Vitro Aurora-B kinase inhibition test
This assay determines the ability of a test compound to inhibit serine-threonine kinase activity. DNA encoding Aurora-B may be obtained by total gene synthesis or by cloning. This DNA may then be expressed in a suitable expression system to obtain polypeptide with serine-threonine kinase activity, hi the case of Aurora-B, the coding sequence was isolated from cDNA by polymerase chain reaction (PCR) and cloned into the pFastBac system in a manner similar to that described above for Aurora-A (i.e. to direct expression of a 6-histidine tagged Aurora-B protein).
For the large scale expression of Aurora-B kinase activity, Sf21 insect cells were grown at 28°C in TC100 medium supplemented with 10% foetal calf serum (Viralex) and 0.2% F68 Pluronic (Sigma) on a Wheaton roller rig at 3 r.p.m. When the cell density reached 1.2x106 cells ml"1 they were infected with plaque-pure Aurora-B recombinant virus at a multiplicity of infection of 1 and harvested 48 hours later. All subsequent purification steps were performed at 4°C. Frozen insect cell pellets containing a total of 2.0 x 108 cells were thawed and diluted with lysis buffer (50 mM HEPES (N-[2-hydroxyethyl]piperazine-N'-[2-ethanesulphonic acid]) pH7.5 at 4°C , 1 mM NaaVCU, 1 mM PMSF (phenylmethylsulphonyl fluoride), 1 mM dithiothreitol, 1 ug/ml aprotinin, 1 ug/ml pepstatin, 1 ug/ml leupeptin), using 1.0 ml per 2 x 107 cells. Lysis was achieved using a sonication homogeniser, following which the lysate was centriruged at 41,000g for 35 minutes. Aspirated supernatant was pumped onto a 5 mm diameter chromatography column containing 1.0 ml CM sepharose Fast Flow (Amersham Pharmacia Biotech) which had been equilibrated in lysis buffer. A baseline level of UV absorbance for the eluent was reached after washing the column with 12 ml of lysis buffer followed by 7 ml of wash buffer (50 mM HEPES pH7.4 at 4°C, 1 mM dithiothreitol). Bound Aurora-B B protein was eluted from the column using a gradient of elution buffer (50 mM HEPES pH7.4 at 4°C, 0.6 M NaCl, 1 mM dithiothreitol, running from 0% elution buffer to 100% elution buffer over 15 minutes at a flowrate of 0.5 ml/min). Elution fractions (1.0 ml)

corresponding to the peak in UV absorbance was collected. Elution fractions were dialysed exhaustively against dialysis buffer (25 mM HEPES pH7.4 at 4°C, 45% glycerol (v/v), 100 mM KC1, 0.05% (v/v) IGEPAL CA630 (Sigma Aldrich), 1 mM dithiothreitol). Dialysed fractions were assayed for Aurora-B kinase activity.
Each new batch of Aurora-B enzyme was titrated in the assay by dilution with enzyme diluent (25 mM Tris-HCl pH7.5,12.5 mM KC1, 0.6 mM DTT). For a typical batch, stock enzyme is diluted 1 in 40 with enzyme diluent and 20|il of dilute enzyme is used for each assay well. Test compounds (at 10 mM in dimethylsulphoxide (DMSO) were diluted with water and lOjil of diluted compound was transferred to wells in the assay plates. 'Total" and "blank" control wells contained 2.5% DMSO instead of compound. Twenty microlitres of freshly diluted enzyme was added to all wells, apart from "blank" wells. Twenty microlitres of enzyme diluent was added to "blank" wells. Twenty microlitres of reaction mix (25 mM Tris-HCl, 78.4 mM KC1, 2.5 mM NaF, 0.6 mM dithiothreitol, 6.25 mM MnCl2, 37.5 mM ATP, 25 |iM peptide substrate [biotin-LRRWSLGLPvRWSLGLRRWSLGLRRWSLG]) containing 0.2u.Ci [733P]ATP (Arnersham Pharmacia, specific activity >2500Ci/mrnol) was then added to all test wells to start the reaction. The plates were incubated at room temperature for 60 minutes. To stop the reaction lOOjxl 20% v/v orthophosphoric acid was added to all wells. The peptide substrate was captured on positively-charged nitrocellulose P30 filtermat (Whatman) using a 96-well plate harvester (TomTek) and then assayed for incorporation of 33P with a Beta plate counter. "Blank" (no enzyme) and "total" (no compound) control values were used to determine the dilution range of test compound which gave 50% inhibition of enzyme activity.
In this test, the compounds of the invention give 50% inhibition of enzyme activity at concentrations of 0.3 nM to 1000 nM and in particular compound 5 in Table 1 gave 50% inhibition of enzyme activity at a concentration of 1.6 nM.
(c) In Vitro cell proliferation assay
This and other assays can be used to determine the ability of a test compound to inhibit the growth of adherent mammalian cell lines, for example the human rumour cell line SW620 (ATCC CCL-227). This assay determines the ability of at test compound to inhibit the incorporation of the thymidine analogue, 5'-bromo-2'-deoxy-uridine (BrdU) into cellular DNA. SW620 or other adherent cells were typically-seeded at IxlO5 cells per well in L-l 5 media (GIBCO) plus 5% foetal calf serum, 1% L-glutamine (100 pi / well) in 96 well tissue

culture treated 96 well plates (Costar) and allowed to adhere overnight. The following day the cells were dosed with compound (diluted from 10 mM stock in DMSO using L-15 (with 5% PCS, 1% L-glutamine). Untreated control wells and wells containing a compound known to give 100% inhibition of BrdU incorporation were included on each plate. After 48 hours in the presence / absence of test compound the ability of the cells to incorporate BrdU over a 2 hour labelling period was determined using a Boehringer (Roche) Cell Proliferation BrdU ELISA kit (cat. No. 1 647 229) according to manufacturers directions. Briefly, 15 p.1 of BrdU labelling reagent (diluted 1:100 in media - L-15, 5% PCS, 1 % L-glutamine) was added to each well and the plate returned to a humidified (+5% €62) 37°C incubator for 2 hours. After 2 hours the labelling reagent was removed by decanting and tapping the plate on a paper towel. FixDenat solution (50 |J.l per well) was added and the plates .incubated at room temperature for 45 minutes with shaking. The FixDenat solution was removed by decanting and tapping the inverted plate on a paper towel. The plate was then washed once with phosphate buffered saline (PBS) and 100 ul /well of Anti-BrdU-POD antibody solution (diluted 1:100 in antibody dilution buffer) added. The plate was then incubated at room temperature with shaking for 90 minutes. Unbound Anti-BrdU-POD antibody was removed by decanting and washing the plate 4 times with PBS before being blotted dry. TMB substrate solution was added (100 fil/well) and incubated for approximately 10 minutes at room temperature with shaking until a colour change was apparent. The optical density of the wells was then determined at 690 nm wavelength using a Titertek Multiscan plate reader. The values from compound treated, untreated and 100% inhibition controls were used to determine the dilution range of a test compound that gave 50% inhibition of BrdU incorporation. The compounds of the invention are active at 0.3 nM to 10000 nM in this test and in particular compound 5 in table 1 was active at 0.1 nM.
(d) In Vitro cell cycle analysis assay
This assay determines the ability of a test compound to arrest cells in specific phases of the cell cycle. Many different mammalian cell lines could be used in this assay and SW620 cells are included here as an example. SW620 cells were seeded at 7 x 10s cells per T25 flask (Costar) in 5 ml L-15 (5% PCS, 1% L-glutamine). Flasks were then incubated overnight in a humidified 37°C incubator with 5% C02. The following day, 5 (il of L-15 (5% PCS, 1% L-glutamine) carrying the appropriate concentration of test compound solubilised in DMSO was added to the flask . A no compound control treatments was also included (0.5% DMSO). The

cells were then incubated for a defined time (24 hours) with compound. After this time the media was aspirated from the cells and they were washed with 5 ml of prewarmed (37°C) sterile PBS A, then detached from the flask by brief incubation with trypsin and followed by resuspension in 5 ml of 1 % Bovine Serum Albumin (BSA, Sigma-Aldrich Co.) in sterile PBS A. The samples were then centrifuged at 2200 rpm for 10 minutes. The supernatant was aspirated to leave 200 jil of the PBS/BSA solution. The pellet was resuspended in this 200 pi of solution by pipetting 10 times to create a single cell suspension. One ml of ice-cold 80% ethanol was slowly added to each cell suspension and the samples stored at -20°C overnight or until required for staining. Cells were pelleted by centrifugation, ethanol aspirated off and pellets resuspended in 200 Jll PBS containing 100 |J,g/ml RNAse (Sigma Aldrich) and 10 |ig/ml Propidium Iodide (Sigma Aldrich). Cell suspensions were incubated at 37°C for SOmin, a further 200 fil PBS added and samples stored in the dark at 4°C overnight.
Each sample was then syringed 10 times using 21-guage needle. The samples were then transferred to LPS tubes and DNA content per cell analysed by Fluorescence activated cell sorting (F ACS) using a FACScan flow cytometer (Becton Dickinson). Typically 30,000 events were counted and recorded using CellQuest vl.l software (Verity Software). Cell cycle distribution of the population was calculated using Modfit software (Verity Software) and expressed as percentage of cells with 2N (GO/G1), 2N-4N (S phase) and with 4N (G2/M) DNA content.
The compounds of the invention are active in this test at 0.3nM to lOOOOnM.
The invention will now be illustrated in the following non limiting examples, in which standard techniques known to the skilled chemist and techniques analogous to those described in these Examples may be used where appropriate, and in which, unless otherwise stated: (i) evaporations were carried out by rotary evaporation in vacua and work up procedures were carried out after removal of residual solids such as drying agents by filtration; (ii) operations were carried out at ambient temperature, typically in the range 18-25°C and in air unless stated, or unless the skilled person would otherwise operate under an atmosphere of an inert gas such as argon;
(iii) column chromatography (by the flash procedure) and medium pressure liquid chromatography (MPLC) were performed on Merck Kieselgel silica (Art. 9385); (iv) yields are given for illustration only and are not necessarily the maximum attainable; (v) the structures of the end products of the formula (I) were generally confirmed by nuclear

(generally proton) magnetic resonance (NMR) and mass spectral techniques; proton magnetic resonance chemical shift values were measured in deuterated dimethyl sulphoxide (DMSO de) (unless otherwise stated) on the delta scale (ppm downfield from tetramethylsilane) using one of the following four instruments
- Varian Gemini 2000 spectrometer operating at a field strength of 300 MHz
- Broker DPX300 spectrometer operating at a field strength of 300MHz
- JEOL EX 400 spectrometer operating at a field strength of 400 MHz
- Broker Avance 500 spectrometer operating at a field strength of 500MHz
Peak multiplicities are shown as follows: s, singlet; d, doublet; dd, double dooblet; t, triplet; q, quartet; qu, quintet; m, multiplet; br s, broad singlet.
(vi) robotic synthesis was carried out using a Zymate XP robot, with solution additions via a
Zymate Master Laboratory Station and stirred via a Stem RS5000 Reacto-Station at 25°C;
(vii) work up and purification of reaction mixtures from robotic synthesis was carried out as
follows: evaporations were carried out in vacua using a Genevac HT 4; column
;hromatography was performed using either an Anachem Sympur MPLC system on silica
jsing 27 mm diameter columns filled with Merck silica (60 urn, 25 g); the structures of the
final products were confirmed by LCMS on a Waters 2890 / ZMD micromass system using
the following and are quoted as retention time (RT) in minutes:
Column: waters symmetry CIS 3.5 pm 4.6x50 mm
Solvent A: H2O
Solvent B: CH3CN
Solvent C : methanol + 5% HCOOH
Flow rate: 2.5 ml / min
Run time: 5 minutes with a 4.5 minute gradient from 0-100% C
Wavelength: 254 nm, bandwidth 10 nm
Mass detector: ZMD micromass
Injection volume 0.005 ml
(viii) Analytical LCMS for compounds which had not been prepared by robotic synthesis was
performed on a Waters Alliance HT system using the following and are quoted as retention
time (RT) in minutes:
Column: 2.0 mm x 5 cm Phenomenex Max-RP 80A
Solvent A: Water
Solvent B: Acetonitrile

Solvent C: Methanol /1% formic acid or Water / 1% formic acid
Flow rate: 1.1 ml / min
Run time: 5 minutes with a 4.5 minute gradient from 0-95% B + constant 5%
solvent C
Wavelength: 254 nm, bandwidth 10 nm
Injection volume 0.005 ml
Mass detector: Micromass ZMD
(ix) Preparative high performance liquid chromatography (HPLC) was performed on either
- Waters preparative LCMS instrument, with retention time (RT) measured in minutes:
Column: p-basic Hypercil (21x100 mm) 5pm
Solvent A: Water / 0.1% Ammonium carbonate
Solvent B: Acetonitrile
Flow rate: 25 ml / min
Run time: 10 minutes with a 7.5 minute gradient from 0-100% B
Wavelength: 254 nm, bandwidth 10 nm
Injection volume 1 - 1.5 ml
Mass detector : Micromass ZMD
- Gilson preparative HPLC instrument, with retention time (RT) measured in minutes:
Column: 21 mm x 15 cmPhenomenex Luna2 CIS
Solvent A: Water + 0.2% trifluoracetic acid,
Solvent B: Acetonitrile + 0.2% trifluoracetic acid
Flow rate: 21ml/min
Run time: 20 minutes with various 10 minute gradients from 5-100% B
Wavelength: 254 nm, bandwidth 10 nm
Injection volume 0.1 -4.0 ml
(x) intermediates were not generally fully characterised and purity was assessed by thin layer
chromatography (TLC), HPLC, infra-red (IR), MS or NMR analysis.
Particular examples of compounds of formula (I) are set out hi the following tables, in which
- represents the point of attachment of the groups in each table to the compound of formula
(I) above each table:

(Table Remove)

Example 1 - Preparation of Compound 1 in Table 1 - Il-f3-(|4-r(5-l2-f(3-fluorophenvnaminol^-oxoethyll-lfl-pyrazoI^-vDaminol-d-methoyyquinazolin-?-Yl}oxy)propvnpiperidin-4-yl}methyl dihydrogen phosphate
Di(terf-butyl) {l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-17?-pyrazol-3-yl)amino]-6-methoxyqumazolin-7-yl}oxy)propyl]piperidin-4-yl}methyl phosphate (400 mg, 0.53 mmol) was suspended in dioxane (20 ml) and treated with a solution of hydrochloric acid (4.0 N) in dioxane (795 )il, 3.18 mmol) at ambient temperature for 15 hours. The solid was recovered by filtration., washed with dioxane, dried in vacua at 50 °C to yield compound 1 in table 1 (360 mg, 94 % yield) :
'H-NMR (DMSO d6, AcOD): 8.88 (s, 1H), 8.27 (s, 1H), 7.61 (m, 1H), 7.35 (m, 3H)3 6.84 (m, 1H), 6.81 (s, 1H), 4.28 (m, 2H), 3.98 (s, 3H), 3.83 (s, 2H), 3.75 (t, 2H), 3.58 (d, 2H), 3.26 (m, 2H), 3.26 (m, 2H), 2.32 (m, 2H), 1.85 (m, 3H), 1.54 (m, 2H) : MS (+ve ESI): 644.5 (M+H)+.
Di(ter/-butyl) {1 -[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]piperidin-4-yl}methyl phosphate, used as the starting material, was obtained as follows:
a) A mixture of 4-benzyloxy-3-methoxybenzaldehyde (157 g, 649 mmol), sodium acetate (106 g, 1.29 mol), hydroxylamine hydrochloride (90 g, 1.29 mol) and acetic acid (500 rnl) was refluxed for 21 hours. The solvent was evaporated and ice / water (1000 ml) was added to the residue forming a sticky solid. The mixture was neutralised with aqueous sodium hydroxide solution then extracted with dichloromethane (2 x 500 ml). The organic solution was washed with 1.0 N sodium hydroxide (100 ml), brine (100 ml) and then dried over magnesium sulphate. Solvent evaporation, trituration of the residue withhexane : ethyl acetate (3:1) and collection of the solid by vacuum filtration yielded 4-ben2yloxy-3~ rnethoxybenzonitrile (123 g, 80 % yield) as a brown solid : 'H-NMR (DMSO d6): 7.38 (m, 7H), 7.19 (m, 1H), 5.18 (s, 2H), 3.80 (s, 3H): MS(-veESI):238(M-H)~.
b) Acetic acid (17 ml) was added slowly to nitric acid (40 ml, 440 mmol) at 5 °C.
Powdered 4-benzyloxy-3-methoxybenzonitrile (10 g, 42 mmol) was added and the mixture
warmed to 23 °C over 10 minutes. An exotherm occurred and the temperature was controlled
at ice / water (1000 ml). After stirring for two hours the yellow solid was collected by suction
filtration, washed with water and dried to yield 4-ben2yloxy-3-methoxy-6-nitrobenzonitrile
(10.1 g, 85 % yield) as a yellow solid :
'H-NMR (DMSO d6): 7.95 (s, 1H), 7.70 (s, 1H), 7.40 (m, 5H), 5.30 (s, 2H), 3.95 (s, 3H): MS (-ve ESI) : 283 (M-H)'.
c) A mixture of 4-benzyloxy-3-methoxy-6-nitrobenzonitrile (46 g, 162 mmol), sodium
bicarbonate (95 g, 1.13 mol), water (750 ml), dichloromethane (550 ml) and
tetrabutylammonium chloride (30 g, 108 mmol) was rapidly stirred at 20 °C and treated with
sodium dithionite (66 g, 379 mmol) portionwise over 2 hours. The mixture was stirred for a
further hour then the phases separated. The aqueous phase was extracted with
dichloromethane (2 x 200 ml) and the combined organic solution washed with water (300 ml)
and dried over magnesium sulphate. The solution was concentrated to 250 ml and 4.0 M
hydrochloric acid in 1,4-dioxane (150 ml, 0.6 mol) added, then diluted with diethyl ether
(1000 ml) and cooled on ice. The resulting solid was collected by vacuum filtration and
washed with diethyl ether. The solid was stirred in methanol (1000 ml) and sodium
bicarbonate solution (800 ml) added to pH 8 and stirred for 1 hour. The solid was collected by
vacuum filtration, washed with water then methanol and dried in vacua to yield 2-amino-4-
(benzyloxy)-5-methoxybenzonitrile (34 g, 82 % yield) as light brown solid :
'H-NMR (DMSO dfi) : 7.40 (m, 5H), 6.90 (s, 1H), 6.50 (s, 1H), 5.60 (br s, 2H), 5.02 (s, 2H),
3.65 (s, 3H):
MS (+ve ESI) : 254 (M+H)+.
d) 2-amino-4-(benzyloxy)-5-methoxybenzonitrile (100 g, 394 mmol) in toluene (1400
ml) was treated with dimethylformamide dimethylacetal (100 ml, 940 mmol) at reflux with
slow distillation of solvent to maintain the internal temperature at 105 °C. After 3 hours the
solution was cooled and filtered to remove a small amount of solid. The filtrate was
evaporated in vacua and the residue triturated with diethyl ether and the solid collected by
vacuum filtration and dried in vacua to yield AP-(5-(benzyloxy)-2-cyano-4-methoxyphenyl)-
JV^-dimethylimidoformamide (110 g, 90 % yield) as a brown solid :
'H-NMk e) A^-(5-(>enzyloxy)-2-cyano-4-methoxyphenyl)-7\^Ar-dimethylirddofonnamide (110 g,
356 rnmol) and trifluoroacetic acid (600 ml) were refluxed together for 15 min. Evaporation
and co-evaporation with toluene, trituration with diethyl ether and collection of the solid by
vacuum filtration and drying in vacua yielded JV-(2-cyano-5-hydroxy-4-methoxyphenyl)-AyV-
dimethylimidoformamide (112 g, 95 % yield) as a light brown trifluoroacetate salt:
JH-NMR (DMSO dfi): 8.39 (s, 1H), 7.38 (s, 1H), 6.90 (s, 1H), 3.80 (s, 3H), 3.25 (s, 3H), 3.17
(s,3H):
MS (+ve ESI) : 220 (M+H)+ MS(-veESI):218(M-H)'.
f) A mixture of 7V-(2~cyano-5-hydroxy-4-methoxyphenyl)-jV,7Y-
dimethyliniidofornianiide (21.9 g, 66 mmol), cesium carbonate (998 g, 300 mmol) and 1-
bromo-3-chloropropane (11 ml, 110 mmol) in acetonitrile (300 ml) was refluxed for 1 hour.
The reaction mixture was cooled and the solvent evaporated in vacua. The residue in water
(200 ml) was extracted with dichloromethane (2 x 150 ml). The organic solution was washed
with brine (50 ml) and dried over magnesium sulphate. Solvent was evaporated in vacua and
the residue triturated with diethyl ether. The solid was collected by vacuum filtration and
dried in vacuo to yield 7V-(5-(3-chloropropoxy)-2-cyano-4-methoxyphenyl)-7^,A':-
dimethylimidoformamide (17.7 g, 91 % yield) as a white solid :
'H-NMR (DMSO d6): 8.89 (s, IH), 7.07 (s, m), 6.75 (s, IH), 4.15 (t, 2H), 3.77 (t, 2H), 3.70
(s, 3H), 3.05 (s, 3H), 2.95 (s, 3H), 2.18 (m, 2H) : MS (+ve ESI): 296.4 (M+H)+.
g) N'-(5-(3-chloropropoxy)-2-cyano-4-methoxyphenyl)-7V^Ar-dimethyluiiidofonnamide
(230 mg, 0.78 mmol) in acetic acid (0.7 ml) was reacted with methyl (5-amino-lH-pyrazol-3-
yl)acetate (CAS 174891-10-2; WO 95/33724) (110 mg, 0.74 mmol) at reflux for 1 hour. The
mixture was cooled, the acetic acid evaporated, and the residue purified by chromatography
on silica gel, eluting with dichloromethane 71% methanolic ammonia (90:10), to give methyl
(5-((7-(3 -chloropropoxy)-6-metlioxyquinazolin-4-yl)amino)-1 H-pyrazol-3-yl)acetate (219
mg, 69 % yield) as a cream solid :
'H-NMR (DMSO d6, TFA): 8.93 (s, 1H), 8.28 (s, IH), 7.32 (s, IH), 6.80 (s, IH), 4.02 (m, 2H), 4.00 (s, 3H), 3.75-3.85 (m, s, 4H), 3.65 (s, 3H), 2.30 (m, 2H), 1.90 (s, 3H) : MS (+ve ESI): 406.5 (M+H)+.
h) Methyl (5-((7-(3-chloropropoxy)-6-methoxyquinazoHn-4-yl)amino)-1 H-pyrazol-3-yl)acetate (100 mg, 0.247 mmol) in tetrahydrofuran (1.2 ml) / water (0.6 ml), was reacted with lithium hydroxide (21 mg, 0.493 mmol) at ambient temperature over night. The mixture was acidified with 6.0 N hydrochloric acid to pH 4 and the solid was recovered by filtration, washed with water and dried to give (5-((7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl)amino)-lH-pyrazol-3-yl)acetic acid (72 mg, 75 % yield) as a beige solid :
'H-NMR (DMSO d6, TFA) : 8.95 (s, m), 8.28 (s, IH), 7.32 (s, m), e.so (s, IH), 4.33 (m,
2H), 4.00 (s, 3H), 3.83 (m, 2H), 3.74 (s, 2H), 2.40-2.50 (m, 2H) : MS (+ve ESI) : 392.5, 394.5 (M+H)+.
i) (5-((7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl)amino)-lH-pyrazol-3-yl) acetic acid (7.83 g, 20 mmol) in dimethylformamide (78 ml) was reacted with 3-fluoroaniliae (2.44 g, 22 mmol) in the presence of l-(3-dimethylamino-propyl)-3-ethylcarbodiimide hydrochloride (4.2 g, 22 mmol), 2-hydroxypyridin-l-oxide (2.22 g, 20 mmol) and diisopropylethylamine (2.8 g, 22 mmol) at 50 °C for 1.7 hours. The solvent was removed by evaporation under vacuum, the residue was triturated with water (twice), and purified by silica gel chromatography, eluting with dichloromethane : methanol (95:3 to 85:15) to give 2-(5-((7-(3-chloropropoxy)-6-memoxyqumazolm-4-yl)amino)-lH-pyrazol-3-yl)-N-(3-fluorophenyl) acetamide (4.5 g, 46 % yield) as a beige solid:
'H-NMR (DMSO d6): 8.47 (s, IH), 8.02 (s, m), 7.60-7.68 (m, m), 7.30-7.41 (m, 2H), 7.20
(s, IH), 6.88 (m, IH), 6.84 (s, IH), 4.27 (m, 2H), 3.96 (s, 3H), 3.84 (m, 2H), 3.78 (s, 2H),
2.26 (m, 2H):
MS (+ve ESI): 485.6 (M+H)+.
j) Piperidin-4-ylmethanol (115 mg, 1 mmol) was added to a solution of 2-(5-((7~(3-
chloropropoxy)-6-rnethoxyquinazolin-4-yl)ammo)-1 H-pyrazol-3 -yl)-N-(3 -fluorophenyl)
acetamide (121 mg, 0.25 mmol) in dimethylacetamide (1 ml) and the reaction was heated at
90 °C for 9 hours. The reaction was cooled to ambient temperature and the volatile substances
removed in vacua. Purification by reverse phase hplc yielded JV-(3-fluorophenyl)-2-{3-[(7-{3-
[4-(hydroxymethyl)piperidin-1 -yljpropoxy} -6-methoxyquuiazolin-4-yl)amino]-1 .£f-pyrazol-5-
yl} acetamide (80 mg, 57 % yield) as an off-white solid:
'H-NMR (DMSO d6, TFA): 8.96 (s, 1H), 8.30 (s, 1H), 7.63 (m, 1H), 7.36 (m, 3H), 6.90 (m,
1H), 6.84 (s, 1H), 4,30 (t, 2H), 4.01 (s, 3H), 3.85 (s, 2H), 3.62 (d, 2H), 3.32 (d, 2H), 3.27 (m,
2H), 2.98 (t, 2H)5 2.29 (m, 2H), 1.90 (d, 2H), 1.67 (m, 1H), 1.42 (m, 2H):
MS (+ve ESI) : 564.6 (M+H)+.
k) A^-(3-fIuorophenyl)-2-{3-[(7-{3-[4-(hydroxymethyl)piperidin-l-yl]propoxy}-6-
memoxyqumazolm-4-yl)ammo]-l#-pyrazol-5-yl}acetamide (450 mg, 1 mmol) was dissolved
in dimethylformarnide (2 ml), tetrazole (224 mg, 4 mmol) and di-ter/-butyl-diethyl-
phosphoramidite (479 fil, 2 mmol) were added to the mixture at ambient temperature, and
stirring was continued for 3 hours under argon. The reaction mixture was then cooled to —60
°C and a solution of monoperoxyphthalic acid magnesium salt (297 mg, 0.6 mmol) in
dimethylformarnide (1.5 ml) was slowly added to the reaction mixture. This mixture was then
stirred for 1.5 hours at -60 °C, sodium metabisulphite (1.5 g, 10 mmol) in solution in water (2
ml) was then added and the reaction mixture was slowly allowed to warm to ambient
temperature, evaporated, and the residue was purified by silica gel chromatography, eluting
with dichloromethane : 3.0 N methanolic ammonia (100:0 to 92:8), to give di(/ert-butyl) {1-
[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-llT-pyrazol-3-yl)amino]-6-
methoxyquinazolin-7-yl}oxy)propyl]piperidin-4-yl}memyl phosphate (420 mg, 70 % yield)
as a cream solid:
'H-NMR (DMSO d6): 8.46 (s, 1H), 7.99 (s, 1H), 7.63 (d, 1H), 7.36 (m, 2H), 7.35 (s, 1H),
7.15 (s, 1H), 6.90 (m, 1H), 6.88 (s, 1H), 4.17 (t, 2H), 3.95 (s, 3H), 3.77 (s, 2H), 3.72 (t, 2H),
2.91 (d, 2H), 2.46 (t, 2H), 1.96 (m, 4H), 1.65 (m, 2H), 1.58 (m, 1H ), 1.41 (s, 18H), 1.25 (m,
2H):
MS (+ve ESI) : 756.6 (M+H)+.
Example 2 - Preparation of Compound 2 in Table 1 - 2-rf3-(|4-f(5-{2-f(3,5-difluorophenyl)amino1-2-oxoethyl|-lfl-pyrazol-3-yl)aminol-6-methoxyquinazolin-7-yl}oxy)propyl1(ethyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(tert-butyY) 2-[[3K{4-[(5-{2-[(3,5-difluorophenyl)arnino]-2-oxoemyl}-l.H-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl phosphate (320 mg, 0.428 mmol) yielded compound 2 in table 1 (260 mg, 86 % yield) as an off-white solid :
'H-NMR (DMSO d6, CD3cooD): 8.92 (s, m), 8.31 (s, m), 7.41 (m, 3H), 6.88 (t, m), 6.84
(s, 1H), 4.32 (m, 4H), 3.97 (s, 3H), 3.89 (s, 2H), 3.42 (m, 6H), 2.32 (m, 2H), 1.31 (t, 3H) :
MS (+ve ESI) : 636.4 (M+H)+.
Di(te^butyl)2-[[3-({4-[(5-{2-[(3,5-dMuorophenyl)arjrLno]-2-oxoe1iiyl}-m-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl phosphate, used as the starting material, was obtained as follows:
a) A suspension of 3-{[7-(3-chloropropoxy)-6-methoxyquinazoUn-4-yl]amino}-l/f-pyrazol-5-yl)acetic acid (3.91 g, 10 mmol) in dimethylformamide (20 ml) was reacted with 3,5-difluoroaniline (1.42 g , 11 mmol) in the presence of l-(3-dimethylaminopropyl)-3-ethylcarbodimide hydrochloride (2.01 g, 10.5 mmol) and 2-hydroxypyridine-l-oxide (1.11 g, 10 mmol) at 60 °C for 1.75 hours. The solvent was evaporated in vacua and the residue was triturated twice with water. The resulting wet paste was dissolved in a mixture of dichloromethane : water (80:20), adsorbed onto silica gel and purified by chromatography on silica gel, eluting with dichloromethane : methanol (95:5 to 85:15) to give 2-(5-((7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl)amino)-lH-pyrazol-3-yl)-N-(3,5-difluorophenyl) acetamide (2.45 g, 49 % yield) as a beige solid :
'H-NMR (DMSO d6): 8.47 (s, IH), 8.02 (s, IH), 7.36 (m, 2H), 7.20 (s, 1H)5 6.94 (t, IH), 6.84 (s, IH), 4.27 (m, 2H), 3.96 (s, 3H), 3.83 (m, 2H), 3.79 (s, 2H), 2.27 (m, 2H) : MS (+ve ESI) : 503.5, 505.5 (M+H)+.
b) An analogous reaction to that described in example Ij, but starting with 2-
(ethylamino)ethanol (89 mg, 1 mmol) and 2-(5-((7-(3-chloropropoxy)-6-methoxyquinazolin-
4-yl)amino)-lH-pyrazol-3-yl)-N-(3,5-difluorophenyl) acetamide (130 mg, 0.26 mmol) yielded
7V-(3,5-difluorophenyl)-2-{3-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}-6-
methoxyquinazolin-4-yl)amino]-l/f-pyrazol-5-yl}acetamide (124 mg, 86 % yield) as an off-
white solid:
'H-NMR (DMSO d6, TFA) : s.96 (s, IH), 8.30 (s, IH), 7.35 (m, 2H), 7.33 (s, IH), 6.90 (m,
IH), 6.84 (s, IH), 4.30 (m, 2H), 4.01 (s, 3H), 3.86 (s, 2H), 3.78 (t, 2H), 3.30 (m, 6H), 2.29 (m,
2H), 1.27(t,3H):
MS (+ve ESI) : 556.5 (M+H)+.
c) An analogous reaction to that described in example Ik, but starting with N-(3,5-
difluorophenyl)-2-{3-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}-6-methoxyquinazolin-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (400 mg, 0.72 mmol) yielded di(fe/-/-butyl) 2-[[3-({4-
[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-17:/-pyrazol-3-yl)amino]-6-
methoxyquinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl phosphate (320 mg, 60 % yield) as an
off-white solid:
'H-NMR (DMSO d6): 8.36 (s, 1H), 7.88 (s, 1H), 7.26 (m, 2H), 7.04 (s, 1H), 6.83 (t, 2H), 6.73 (s, 1H), 4.07 (m, 2H), 3.85 (s, 3H), 3.77 (q, 2H), 2.68 (s, 2H), 2.55 (m, 4H), 2.43 (m, 2H), 1.81(m,2H),0.88(t,3H): MS C+ve ESI) : 748.5 (M+H)+.
Example 3 - Preparation of Compound 3 in Table 1 - ((2>Sf)-l-r3-fl4-rr5-(2-fr3.5-difluorophenyl)amino1-2-oxoethyI}-lg-pyrazol-3-yl)amino1-6-methoxyquinazoIin-7-yl|oxy)propyI]pyrrQlidin-2-yI|methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(/er?-butyl) {(IS)-1 -[3-( {4-[(5- {2-[(3,5-difluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl phosphate (130 mg, 0.171 nxmol) yielded compound 3 in table 1 (91 mg, 74 % yield) ;:
'H-NMR (DMSO d6, CD3COOD): 8.91 (s, 1H), 8.29 (s, 1H), 7.40 (m, 3H), 6.89 (t, 1H), 6.82 (s, 1H), 4.31 (m, 2H), 4.20 (m, 2H), 4.00 (s, 3H), 3.88 (s, 2H), 3.80 (m, 1H), 3.70 (m, 1H), 3.60 (m, 1H), 3.28 (m, 1H), 3.23 (m, 1H), 2.30 (m, 2H), 2.20 (m, 1H), 2.03 (m, 1H), 1.95 (m,lH), 1.82 (m,lH): MS (+ve ESI) : 648.3 (M+H)+.
di(tert-butyl) {(26)-l-[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazolui-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate, used as the starting material, was obtained as follows:
a) An analogous reaction to that described in example 2b, but starting with L-prolinol
(101 mg, 1 mmol) yielded A^-(3,5-difluorophenyl)-2-{3-[(7-{3-[(2S)-2-
(hydroxymernyl)pyrrolidrn-l-yl]propoxy}-6-mernoxyqurnaz^
yl}acetamide (85 mg, 57 % yield) as an off-white solid :
'H-NMR (DMSO d6) TFA): 8.96 (s, 1H), 8.30 (s, 1H), 7.30-7.40 (m, 3H), 6.85-6.95 (m, 1H),
6.84 (s, 1H), 4.30 (m, 2H), 4.01 (s, 3H), 3.86 (s, 2H), 3.72-3.82 (m, 1H), 3.50-3.70 (m, 4H),
3.15-3.30 (m, 2H), 2.25-2.40 (m, 2H), 1.95-2.20 (m, 2H), 1.85-1.95 (m, 1H), 1.70-1.85 (m,
1H):
MS (+ve ESI): 568.6 (M+H)+.
b) ?/-(3,5-difluorophenyl)-2-{3-[(7-{3-[(25)-2-(hydroxymethyl)pyrrolidin-l-
yl]propoxy}-6-methoxyquinazolin-4-yl)amino]-l/f-pyrazol-5-yl}acetamide (650 mg, 1.14
mmol) was dissolved in dimethylacetamide (4 ml). Tetrazole (160 mg, 2.3 mmol) and di-tert-
butyl-diethylphosphoramidite (637 [il, 2.3 mmol) were added to the mixture and stirring was
continued at ambient temperature under argon for 3 hours. The reaction mixture was then diluted with dichloromethane (50 ml) and washed with a saturated solution of sodium bicarbonate. The organic phase was recovered, dried over magnesium sulphate, filtered and concentrated. The crude product was dissolved in tetrahydrofuran (18 ml) at 0 °C and i hydrogen peroxide (30 %, 335 |xl) was added to the solution, which was stirred for 15 hours at ambient temperature. The mixture was then cooled to 0 °C and sodium metabisulphite (1.08 g) in water (5 ml) was added at 0 °C, and the reaction was allowed to warm to ambient temperature. The mixture was diluted with ethyl acetate (50 ml), washed with a saturated solution of sodium bicarbonate. The organic phase was recovered, dried over magnesium sulphate, filtered and concentrated in vacua. The crude product was purified by chromatography on silica gel, eluting with dichloromethane : methanol: 3.0 Nmethanolic ammonia (95:5:0 to 95:0:5), to give di(ter?-butyl) {(26)-l-[3-({4-[(5-{2-[(3,5-difluorophenyl)ammo]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (133 mg, 15 % yield) as an off-white solid: 'H-NMR (DMSO d6): 8.44 (s, 1H), 7.96 (s, 1H), 7.35 (m, 2H), 7.13 (s, 1H), 6.92 (m, 1H), 6.82 (s, 1H), 4.18 (m, 2H), 3.93 (s, 3H), 3.75 (m, 3H), 3.56 (m, 1H), 3.08 (m, 1H), 2.92 (m, 1H), 2.67 (m, 1H), 2.46 (m, 1H), 2.20 (q, 1H), 1.95 (m, 2H), 1.83 (m, 1H), 1.68 (m, 2H), 1.59 (m, 1H), 1.38 (s, 18H) : MS (+ve ESI): 760.5 (M+H)+.
Example 4 - Preparation of Compound 4 in Table 1 - K2J?)-l-r3-f|4-rf5-l2-rf3.5-difluorophenyl)ainino1-2-oxoethyl|-lJ3r-pvrazoI-3-yl)amino1-6-methoxvqiiinazolin-7-yl}oxy)propyl]pyrrolidin-2-yI}methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(tert-butyl) {(2£)4-[3 memoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (350 mg, 0.46 mmol) yielded compound 4 in table 1 (305 mg, 92 % yield) as an off-white solid : ]H-NMR (DMSO d di(re^butyl){(2^)-l-[3-({4-t(5-{2-[(335-difluorophenyl)amino]-2-oxoethyl}-lJ:r-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate, used as the starting material, was obtained as follows:
a) An analogous reaction to that described in example 2b, but starting with D-prolinol
(101 mg, 1 mmol) yielded 7V-(3,5-difluorophenyl)-2-{3-[(7-{3-[(2R)-2-
(hydroxymethyl)pyrrolidm-l-yl]propoxy}-6-memoxyqumazolm-4-yl)ammo]-lff-pyrazol-5-
yljacetamide (85 mg, 57 % yield) as an off-white solid :
'H-NMR (DMSO d6, TFA) : 8.96 (s, m), s.so (s, IH), 7.35 (m, 2H), 7.33 (s, IH), 6.91 (m,
IH), 6.84 (s, IH), 4.31 (m, 2H), 4.01 (s, 3H), 3.86 (s, 2H), 3.78 (m, IH), 3.63 (m, 4H), 3.22 (m, 2H)3 2.30 (m, 2H), 2.13 (m, IH), 2.03 (m, IH), 1.80 (m, IH), 1 .78 (m, IH) : MS (+ve ESI) : 568.5 (M+H)+.
b) An analogous reaction to that described in example 3b, but starting with JV-(3,5-
difluorophenyl)-2-{3-[(7-{3-[(2^)-2-(hydroxymethyl)pyrrolidin-l-yl3propoxy}-6-
memoxyquinazolin-4-yl)aniino]-lH-pyrazol-5-yl}acetamide (600 mg, 1.06 mmol) yielded
di(tert-butyl) {(2/?)-l-[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-lH'-pyrazol-3-
yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (361 mg,
45 % yield) as an off-white solid :
'H-NMR (DMSO d6): 8.45 (s, m), 7.96 (s, m), 7.35 (m, 2H), 7.13 (s, m), 6.93 (m, m),
6.82 (s, IH), 4.18 (m, 2H), 3.95 (s, 3H), 3.75 (m, 3H), 3.58 (m, IH), 3.08 (m, IH), 2.93 (m, IH), 2.67 (m, IH), 2.46 (m, IH), 2.22 (q, IH), 1.96 (m, 2H), 1.86 (m, IH), 1.69 (m, 2H), 1.61 (m, IH), 1.38(s, 18H): MS (+ve ESI) : 760.5 (M+H)+.
Example 5 - Preparation of Compound 5 in Table 1 - {(2iy)-l-[3-(j4-r(5-{2-rf3-fluorophenvDaminol^-oxoethyU-lff-pyrazol-S-vDaininol^-inethoxvquinazolin^-yl}oxy)propvl1pyrrolidin-2-vl}methyI dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(ter/-butyl) {(25)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoe%l}-lF-pyrazol-3-yl)aniino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methylphosphate (282 mg, 0.38 mmol) yielded compound 5 in table 1 (265 mg, 97 % yield) as an off-white solid : 'H-NMR (DMSO d6): 8.90 (s, IH), 8.30 (s, IH ), 7.66 (d, IH), 7.46 (s, IH), 7.40 (m, 2H), 6.90 (m, IH), 6.81 (s, IH), 4.31 (m, 2H), 4.20 (m, 2H), 4.00 (s, 3H), 3.88 (s, 2H), 3.80
(m, IH), 3.70 (m, IH), 3.60 (m, IH), 3.28 (m, IH), 3.22 (m, IH), 2.32 (m, 2H), 2.20 (m,
IH), 2.04 (m, IH), 1.95 (m, IH), 1.84 (m, IH):
MS (+ve ESI): 630.6 (M+H)+.
di(rert-butyl) {(2,S)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJff-pyrazol-3-
yl)amino]-6-niethoxyquinazolin-7-yI}oxy)propyl]pyrrolidin-2-yl}methyl phosphate, used as
the starting material, was obtained as follows:
a) An analogous reaction to that described in example Ij, but starting with L-prolinol
(121 mg, 0.25 mmol) yielded A^-(3-fluorophenyl)-2-{3-[(7-{3-[(25)-2-
(hydroxymethyl)pyrrolidin-1 -yljpropoxy} -6-methoxyquinazolin-4-yl)amino]- l#-pyrazol-5-
yl}acetamide (86 mg, 62 % yield) as an off-white solid :
'H-NMR (DMSO dg, TFA) : 8.95 (s, IH), 8.29 (s, m), 7.60-7.70 (m, IH), 7.28-7.40 (m, 3H),
6.85-6.92 (m, IH), 6.82 (s, IH), 4.31 (m, 2H), 4.00 (s, 3H), 3.84 (s, 2H), 3.70-3.80 (m, IH), 3.50-3.70 (m, 4H), 3.10-3.30 (m, 2H), 2.20-2.40 (m, 2H), 2.05-2.20 (m, IH), 1.95-2.10 (m, IH), 1.85-1.95 (m, IH), 1.70-7.85 (m, IH) : MS (+ve ESI): 549.6 (M+H)+.
b) An analogous reaction to that described in example Ik, but starting with JV-(3-
fluorophenyl)-2-{3-[(7-{3-[(21S)-2-(hydroxymethyl)pyrroUdin-l-yl]propoxy}-6-
methoxyqumazolm-4-yl)amino]-lff-pyrazol-5-yl}acetamide (275 mg, 0.5 mmol) yielded
di(tert-butyl) {(25)-1 -[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoemyl} -ltf-pyrazol-3-
yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}rnethyl phosphate (255 mg,
69 % yield) as an off-white solid :
'H-NMR (DMSO d6): 8.46 (s, IH), 7.98 (s, IH), 7.64 (d, IH), 7.36 (m, 2H), 7.15 (s, IH), 6.89 (m, IH), 6.81 (s, IH), 4.18 (m, 2H), 3.93 (s, 3H), 3.75 (m, 3H), 3.58 (m, IH), 3.11 (m, IH), 2.97 (m, IH), 2.67 (m, IH), 2.46 (m, IH), 2.22 (m, IH), 1.98 (m, 2H), 1.82 (m, IH), 1.71 (m, 2H), 1.62 (m, IH), 1.38 (s, 18H): MS (+ve ESI) : 742.7 (M+H)+.
Example 6 - Preparation of compound 6 in table 1 - 2-rr3-(|4-f(5-{2-[(2,3-lifluorophenyl)amino1-2-oxoethv[}-ljy-pvrazol-3-yl)amino1-6-methoxvquinazolin-7-d|oxv)propvn(propyl)amino]ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-ter*-butyl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-
methoxyquinazolin-7-yl}oxy)propyl](propyl)amino]ethyl phosphate (316 nig, 0.41 mmol) yielded compound 6 in table 1 (300 mg, 100 % yield) :
'H-NMR (DMSO d6>TFA): 8.96 (s, 1H), 8.31 (a, 1H), 7.75 (m, 1H), 7.36 (s, 1H), 7.20 (m, 2H), 6.84 (s, 1H), 4.31 (t, 2H), 4.24 (m, 2H), 4.01 (s, 3H), 3.94 (s, 2H), 3.50 (m, 2H), 3.38 (m, 2H), 3.19 (m, 2H), 2.32 (m, 2H), 1.74 (m, 2H), 0.95 (t, 3H): MS (+ve ESI) : 650.3 (M+H)+.
di-fcrt-butyl 2-[[3-( (4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} -l/f-pyrazol-3-yl)amino]-6-methoxyquinazolm-7-yl}oxy)propyl](propyl)amino]ethyl phosphate used as starting material was obtained as follows :
a) 5-{[7-(3-cUoropropoxy)-6-methoxyqumazolm-4-yl]arnino}-lH-pyrazol-3-yl)acetic acid (3.91 g, 10 mmol) was suspended in pyridine (20 ml) in the presence of 2,3-difluoroaniline (1.55 g, 12 mmol) under argon at 0 °C. Phosphorus oxychloride (1.53 g, 10 mmol) in ethyl acetate (2 ml) was slowly added at 0 °C and the resulting mixture was allowed to warm to ambient temperature over 1.5 hours. The reaction mixture was diluted with ethyl acetate (150 ml) and diethyl ether (50 ml) resulting in the precipitation of a red solid. The solid was recovered by suction filtration, dried and re-suspended in water (100 ml). The mixture was cooled to 0 °C and the pH adjusted to 7 by addition of 1.5 N aqueous ammonium hydroxide solution. After 15 minutes stirring, the solid was recovered, dried, and purified by chromatography on silica gel, eluting with dichlorornethane : methanol (95/5) and increased polarity to dichlorornethane : methanolic ammonia (95:2) to yield 2-(3-{[7-(3-cUoropropoxy)-6-methoxyqumazolin-4-yl]amino}-llZ-pyrazol-5-yl)-JV"-(2,3-difluorophenyl)acetamide as a pink solid (2.55 g, 50 % yield) :
'H-NMR (DMSO d6, TFA) : 8.94 (s, m), 8.28 (s, m), 7.73 (m, m), 7.33 (s, m), 7.15-7.22
(m, 1H), 6.84 (s, 1H), 4.30 (m, 2H), 4.00 (s, 3H), 3.94 (s, 2H), 3.84 (m, 2H), 2.30 (m, 2H) : MS (+ve ESI): 503.9 (M+H)+.
b) 2-(propylamino)ethanol (700mg, 68mmol) and potassium iodide (564 mg, 34 mmol) were added to a solution of 2-(3-{[7-(3-chloropropoxy)-6-methoxyquinazolin-4-ylJamino}-l#-pyrazol-5-yl)-N-(2,3-difluorophenyl)acetamide (855 mg, 17 mmol) in dimethylacetamide (8 ml) and the reaction heated at 85 °C for 5 hours. The solvent was evaporated in vacuo, the residue triturated with diethyl ether and the solid was collected by suction filtration. Purification by chromatography on silica gel, eluting with, dichlorornethane / methanol (90:10) to dichloromethane / methanol / ammonia (7.0 N) to give JV-(2,3-difluorophenyl)-2-

{3-[(7-{3-[(2-hydroxyethyl)(propyl)amino]propoxy}-6-methoxyqiiinazolin^-yl)amino]-l/?-pyrazol-5-yl}acetamide (650mg, 67 % yield) :
'H-NMR (DMSO d6, TFA) : 8.96 (S,.IH), 8.30 (s, IH), 7.75 (m, m)3 7.33 (s, m), 7.18-7.22
(m, 2H), 6.84 (s, 1H)5 4.30 (m, 2H), 4.00 (s, 3H), 3.94 (s, 2H), 3.78 (m, 2H), 3.30-3.45 (m, 2H), 3.28 (m, 2H), 3.15-3.20 (m, 2H), 2.28 (m, 2H), 1.73 (m, 2H), 0.95 (t, 3H) : MS (+ve ESI) : 570.3 (M+H)+.
c) Di-ter/'-butyl-diethylphosphoramidite (417 urn, 1.5 mmol) was slowly added to a solution of N-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(propyl) amino]propoxy}-6-methoxyquinazolm-4-yl)amino]-l/f-pyrazol-5-yl}acetamide (569 mg, 1 mmol) in dimethylformarmde (2.5 ml) in the presence of tetrazole (210 mg, 3 mmol) at ambient temperature under argon. The mixture was stirred at ambient temperature for 1.5 hours, cooled to —10 °C and hydrogen peroxide (134 um of a 9.0 N solution, 1.2 mmol) was slowly added. The resulting mixture was stirred at ambient temperature for 2 hours. Sodium metabisulphite (570 mg, 3 mmol) in water (2 ml) was then added at 0 °C and the mixture was stirred at ambient temperature for 0.5 hour. The mixture was concentrated, dichloromethane / methanol (8:2) was added before the solid was filtered and washed with dichloromethane / methanol. Concentration of the filtrate in vacua followed by chromatography on silica gel, eluting with dichloromethane / methanol (90:10) to dichloromethane / methanol / ammonia (7.0 N) (90:10:1), yielded di-tert-buryl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2- . oxoethyl} - lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-
yl}oxy)propyl](propyl)amino]ethyl phosphate as an off-white solid (319 nig, 42 % yield) : ]H-NMR (DMSO d6, TFA) : 8.95 (s, IH), 8.29 (s, IH), 7.72 (m, IH), 7.33 (s, IH), 7.18 (m, 2H), 6.84 (s, IH), 4.20-4.35 (m, 4H), 4.00 (s, 3H), 3.94 (s, 2H), 3.53 (m, 2H), 3.39 (m, 2H), 3.20 (m, 2H), 2.30 (m, 2H), 1.73 (m, 2H), 1.44 (s, 18H), 0.95 (t, 3H) : MS (+ve ESI) : 762.5 (M+H)+.
Compound 6, synthesised above as the dihydrochloride salt, could also be prepared as the free base according to the following method:
d) 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](propyl)amino] ethyl dihydrogen phosphate iihydrochloride (10 g, 13 mmol) was solubilized in methanol (300 ml) and cyclohexane oxide (12,7 g, 130 mmol) was added to the solution. The solution was stirred at ambient temperature for 48 hours, during which time a white solid precipitated. The mixture was diluted with diethyl ether (100 ml) and the solid was recovered by filtration, washed with ether and dried

in vacuo to give 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-
yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](propyl)amino]ethyldihydrogen phosphate
(7.65 g, 88 % yield) as a light yellow powder:
'H-NMR (DMSO d6, TFA): 8.96 (s, 1H), 8.30 (s, 1H), 7.74 (m, 1H), 7.34 (s, 1H), 7.19 (m,
2H), 6.84 (s, 1H), 4.31 (m, 2H), 4.24 (m, 2H), 4.01 (s, 3H), 3.94 (s, 2H), 3.51 (m, 2H), 3.38
(m, 2H), 3.18 (m, 2H), 2.29 (m, 2H), 1.73 (m, 2H), 0.96 (t, 3H) :
MS (+ve ESI): 650 (M+H)+.
C28H34F2N7O7P + 1.04 H20 +0.03 Et20 requires C, 50.37%; H, 5.47%; N, 14.62%; Found C,
50.02%; H, 5.54%; N, 14.48%.
Example 7 - Preparation of compound 7 in table 1 - 2-rr3-((4-f(5-(2-f(2,3-difluorophenyDaminol-l-oxoethyU-lfl-pyrazoI-S-yDaminol-fi-methoxyquinazoIin-?-yl}oxv)propylKisobutyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amko]-2-oxoethyl}-lH'-pyrazol-3-yl)arnino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl phosphate (465 mg, 0.6 mmol) yielded compound 7 in table 1 (480 mg, 100 % yield) :
tefMR (DMSO dfi, TFA) : 8.95 (s, 1H), 8.34 (s, 1H), 7.76 (m, 1H), 7.43 (s, 1H), 7.18 (m, 2H), 6.86 (s, 1H), 4.33 (m, 4H), 4.02 (s, 3H), 3.97 (s, 2H), 3.54 (m, 2H), 3.40 (m, 2H), 3.12 (d, 2H), 2.35 (m, 2H), 2.17 (m, 1H), 1.05 (d, 6H).
di-ter/-butyl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-17f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl phosphate used as starting material was obtained as follows :
a) A cooled (-60 °C) solution of ethylene oxide (5.28 g, 120 mmol) in methanol (14 ml),
was added slowly to a solution of isobutylamine (30.7 g, 420 mmol) in methanol (100 ml) at
-65 °C under argon. The mixture was allowed to warm to ambient temperature over 14 hours,
concentrated in vacuo and the residual oil was purified by distillation (b.p. 130 °C / 0.5
rnmHg) to yield 2-(isobutylamino)ethanol (11 g, 78 % yield) :
'H-NMR (DMSO dfi): 4.40 (m, 1H), 3.42 (m, 2H), 2.50 (m, 2H), 2.30 (d, 2H), 1.63 (m, 1H), 0.85 (d, 6H).
b) An analogous reaction to that described in example 6b, but starting with 2-
(isobutylamino)ethanol (936 mg, 80 mmol) and heating at 90 °C for 3.5 hours, yielded ^V-
(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyemyl)(isobutyl)amino]propoxy}-6-

methoxyquinazolin-4-yl)amino]-lJ1J-pyrazol-5-yl}acetainide as an off-white solid (810 mg, 69
% yield):
'H-NMR (DMSO d& TFA): 8.96 (s, IH), 8.30 (s, IH), 7.45 (m, IH), 7.34 (s, IH), 7.21 (m,
2H), 6.84 (s, IH), 4.31 (m, 2H), 4.00 (s, 3H), 3.95 (s, 2H), 3.81 (m, 2H), 3.36 (m, 2H), 3.30
(m, 2H), 3.12 (m, IH), 3.06 (m, IH), 2.31 (m, 2H), 2.13 (m, IH), 1.01 (d, 6H) :
MS (+ve ESI): 584.3 (M+H)+.
c) An analogous reaction to that described to that described in example 6c, but starting
withA^(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(isobutyl)amino]propoxy}-6-
memoxyquinazolm-4-yl)ammo]-l#-pyrazol-5-yl}acetamide (4.96 mg, 8.5 mmol) yielded di-
/er^buty!2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoemyl}-l^-pyrazol-3-yl)amino]-
6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl phosphate (4.7 g, 71 % yield) :
'H-NMR (DMSO d6, TFA) : 8.96 (s, IH), 8.30 (s, IH), 7.74 (m, IH), 7.34 (s, IH), 7.19 (m,
2H), 6.84 (s, IH), 4.30 (m, 4H), 4.00 (s, 3H), 3.94 (s, 2H), 3.54 (m, 2H), 3.39 (m, 2H), 3.12
(d, 2H), 2.32 (m, 2H), 2.14 (m, IH), 1.45 (s, 18H), 1.02 (d, 6H) :
MS (+ve ESI): 776.8 (M+H)+.
Example 8 - Preparation of compound 8 in table 1 - 2-f[3-(|4-f(5-f2-r(3,5-difluorophenyl)amino1-2-oxoethyl|-lg-pYrazoI-3-yl)amino1-6-metho3cyquinazolin-7-yl}oxy)propyl1(isobutvl)amino1ethvl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)ammo]-2-oxoemyl}-l/f-pyrazol-3-yl)amino]-6-memoxyqumazolm-7-yl}oxy)propyl](isobutyl)ammo]ethyl phosphate (325 mg, 0.42 mmol) yielded compound 8 in table 1 (315 mg, 98 % yield):
'H-NMR (DMSO dfi, TFA): 8.95 (s, IH), 8.32 (s, IH), 7.39 (d, IH), 7.38 (s, IH), 7.36 (d, IH), 6.91 (t, IH), 6.84 (s, IH), 4.30 (m, 2H), 4.01 (s, 3H), 3.87 (s, 2H), 3.53 (m, 2H), 3.39 (m, 2H), 3.11 (d, IH), 2.32 (m, 2H), 2.14 (m, IH), 1.02 (d, 6H): MS (+ve ESI): 664.3 (M+H)+.
di-ter^butyl2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]--2-pxoethyl}-l^'-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino] ethyl phosphate used as starting material was obtained as follows :
a) 2-(3-{[7-(3-chloropropoxy)-6-memoxyquinazolm-4-yl]amino}-lff-pyrazol-5-yl)-JV'-(3,5-difluorophenyl)acetamide (2.0 g, 4.0 mmol) in l-methyl-2-pyrrolidinone (20 ml), potassium iodide (1.33 g, 8.0 mmol) was reacted with 2-(isobutylamino)ethanol (1.88 g, 16

mmol) under argon, at 60 °C for 8 hours. The solvent was evaporated in vacua, and the residue was purified hy chromatography on silica gel, eluting with dichloromethane / methanol (95:5) to dichloromethane / methanol / ammonia (7.0 N) (95:5:1) to yield A/"-(3,5-difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(isobutyl)amino]propoxy}-6-methoxyquinazolin-4-yl)amino]-l-H-pyrazol-5-yl}acetarnide (1.05 g, 45 % yield) : 'H-NMR (DMSO d6, TFA): 8.95 (s, 1H), 8.29 (s, 1H), 7.35 (d, 2H), 7.34 (s, 1H), 6.92 (t, 1H), 6.83 (s, 1H), 4.30 (m, 2H), 4.00 (s, 3H), 3.86 (s, 2H), 3.82 (t, 2H), 3.89 (m, 2H), 3.29 (m, 2H), 2.17-2.98 (m, 2H), 2.30 (m, 2H), 2.13 (m, 1H), 1.01 (d, 6H) : MS (+ve ESI) : 584.3 (M+H)+.
b) Di-^ert-butyl-diethylphosphoramidite (1.25 ml, 4.18 mmol) was slowly added to a solution of JV-(3,5-difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyetliyl)(isobutyl)amino]propoxy}-6-methoxyquinazoUn-4-yl)amino]-lJ:f-pyrazol-5-yl}acetamide (1.03 g, 1.73 mmol) in dimethylformarnide (6 ml) in the presence of tetrazole (431 mg, 6.16 mmol). The mixture was stirred at ambient temperature for 2 hours before dichloromethane (30 ml) was added. The resulting mixture was washed with a saturated solution of sodium bicarbonate (15 ml), the aqueous phase was extracted with dichloromethane (3 x 25 ml), dried and concentrated in vacua. The crude product was dissolved in tetrahydrofuran (25 ml), cooled to 0 °C and hydrogen peroxide (30% w/w, 0.40 ml, 3.9 mmol) was slowly added to the solution. The reaction was stirred for 2 hours at ambient temperature, cooled to 0 °C, and treated with a solution of sodium metabisulphite (1.08 g, 5.7 mmol) hi water (2 ml). The mixture was stirred for 0.5 hour at ambient temperature, diluted with ethyl acetate (30 ml), washed with aqueous sodium bicarbonate solution (15 ml) and extracted twice with ethyl acetate (20 ml) Solvent evaporation in vacua followed by purification by chromatography on silica gel, eluting with dichloromethane / methanol (98:2) to dichloromethane / methanol / ammonia (7.0 N) (95:5:1) yielded di-terf-butyl 2-[[3-( {4-[(5- {2-[(3,5-difluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl phosphate (335 mg, 25 % yield):
'H-NMR (DMSO d6, TFA) : 12.35 (s, IH), io.64 (s, m), 10.16 (s, m), 8.45 (s, m), 7.99 (s,
1H), 7.36 (d, 2H), 7.13 (s, IH), 6.94 (t, IH), 6.84 (s, IH), 4.19 (t, 2H), 3.95 (s, 3H), 3.87 (q, 2H), 3.79 (s, 2H), 2.65 (m, 4H), 2.21 (d, 2H), 1.91 (m, 2H), 1.70 (m, IH), 1.39 (s, 18H), 0.83 (d, 6H): MS (+ve ESI): 776.4 (M+H)+.

Example 9 - Preparation of compound 9 in table 1 - 2-f r3-g4-f(5-l2-rf3.5-difluorophenvl)amino]-2-oxoethvU-lg-pyrazol-3-yl)amino1-6-methoxvquinazoIin-7-vl)oxv)propvl1(propyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1 but starting with di-ter/-butyl 2-[[3 'H-NMR (DMSO d& TFA) : 8.94 (s, IH), 8.31 (s, IH), 7.38 (d, IH), 7.37 (s, 2H), 7.36 (d, IH), 6.92 (t, IH), 6.83 (s, IH), 4.30 (t, 2H), 4.24 (t, 2H), 4.00 (s, 3H), 3.87 (s, 2H), 3.49 (t, 2H), 3.36 (t, 2H), 3.18 (t, 2H), 2.26-2.36 (m, 2H), 1.68-1.79 (m, 2H), 0.94 (t, 3H) : MS (+ve ESI) : 649.9 (M+H)+.
di-to-^butyl2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-lF-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](propyl)amino]ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 8a, but starting with 2-
(propylamino)ethanol (1.83 ml, 16 mmol) yielded JV-(3,5-difluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyemyl)(propyl)amLno]propoxy}-6-memoxyquibazolm-4-yl)amino]-lH"-pyrazol-5-
yl}acetamide (900 mg, 39 % yield):
'H-NMR (DMSO d6) : 10.63 (s, IH), 10.17 (s, IH), 8.46 (s, IH), 8.00 (s, IH), 7.36 (d, 2H),
7.14 (s, IH), 6.94 (t, IH), 6.85 (s, IH), 4.35 (br s, IH), 4.20 (t, 2H), 3.95 (s, 3H), 3.79 (s, 2H),
3.46 (m, 2H), 2.63 (m, 2H), 2.52 (m, 2H), 2.42 (m, 2H), 1.92 (m, 2H), 1.42 (m, 2H), 0.83 (t,
3H):
MS (+ve ESI): 570.3 (M+H)+.
b) An analogous reaction to that described in example 8b, but starting with N-(3,5-
difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(propyl)amino]propoxy}-6-
niethoxyquuiazolin-4-yl)arnino]-17ir-pyrazol-5-yl}acetamide (880 mg, 1.54 mmol) yielded di-
rer/-butyl2-[[3 6-methoxyquinazolin-7-yl}oxy)propyl](propyl)amino]ethyl phosphate (525 mg, 45 % yield) :
'H-NMR (DMSO d6, TFA) : 12.35 (s, m), io.63 (s, m), 10.16 (s, m), 8.45 (s, m), 7.99 (s,
IH), 7.37 (d, IH), 7.34 (d, IH), 7.13 (s, IH), 6.94 (t, IH), 6.84 (s, IH), 4.17 (t, 2H), 3.94 (s,
3H), 3.87 (q, 2H), 3.79 (s, 2H), 2.67 (t, 2H), 2.63 (t, 2H), 2.43 (t, 2H), 1.91 (t, 2H), 1.39 (s,
18H),0.83(t,3H):
MS (+ve ESI): 762.6 (M+H)+.

Example 10 - Preparation of compound 10 in table 1 - 2-rr3-ri4-f(5-|2-f(3-fluorophenyI)aminQl-2-oxoethyl}-lg-pvrazol-"3-vI)amino1-6-methoxyqutnazolin-7-YUoxy)propyI1(isobutyl)amino1ethyI dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-fert-butyl 2-[[3 JH-NMR (DMSO d6, TFA) : 8.90 (s, 1H), 8.30 (s, 1H), 7.64 (m, 1H), 7.36 (m, 3H), 6.85 (m, 2H), 4.30 (m, 4H), 4.00 (s, 3H), 3.86 (s, 2H), 3.53 (m, 2H), 3.37 (m, 2H), 3.09 (m, 2H), 2.34 (m, 2H), 2.14 (m, 1H), 1.05 (m, 6H) : MS (+ve ESI): 646.6 (M+H)+.
di-te7-/-butyl 2-[[3-({4-[(5- {2-[(3-fluorophenyl)ammo]-2-oxoethyl} -lJY-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl phosphate used as starting material was obtained as follows :
i a) An analogous reaction to that described in example 5a, but starting with 2-(isobutyl amino)ethanol (181 mg, 1.55 mmol) yielded JV-(3-fluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(isobutyl)amino]propoxy}-6-methoxyquinazoma-4-yl)arnino]-lZf-pyrazol-5-yl}acetamide (101 rng, 57 % yield): 'H-NMR (DMSO d6, TFA) : 8.96 (s, 1H), 8.30 (s, 1H), 7.63 (d, 1H), 7.32-7.41 (m, 2H), 7.34
' (s, 1H), 6.90 (t, 1H), 6.83 (s, 1H), 4.30 (t, 2H), 4.00 (s, 3H), 3.84 (s, 2H), 3.80 (t, 2H), 3.37 (t, 2H), 3.28 (t, 2H), 3.15-3.00 (m, 2H), 2.29 (m, 2H), 2.12 (m, 2H), 1.00 (d, 6H): MS (+ve ESI): 566.3 (M+H)+.
b) An analogous reaction to that described in example 5b, but starting with JV-(3-fluorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(isobutyl)amino]propoxy} -6-methoxyquinazolin-4-yl)amino]-l#-pyrazol-5-yl}acetarnide (565 mg, 1 mmol) yielded di-ter/-butyl 2-[[3-({4-[(5-(2-[(3-fluorophenyl)amino]-2-oxoethyl}-17:/'-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl](isobutyl)amino]ethyl phosphate (420 mg, 55 % yield): 'H-NMR (DMSO d6, TFA) : 8.37 (s, 1H), 7.88 (s, 1H), 7.55 (m, 1H), 7.26 (m, 2H), 7.04 (s, 1H), 6.81 (rn, 2H), 4.09 (t, 2H), 3.82 (s, 3H), 3.76 (m, 2H), 3.67 (m, 2H), 2.57 (m, 4H), 2.11 (m, 2H), 1.82 (m, 2H), 1.60 (m, 1H), 1.29 (s, 18H), 0.74 (d, 6H) : MS (+ve ESI): 758.5 (M+H)+.

Example 11 - Preparation of compound 11 in table 1 - 2-((2,2-dimethvlpropyI)[3-(|4-f(5-^-[O-fluorophenynaminol^-oxoethyD-lff-pyrazol-S-yDaminol-e-methoryquinazolin-?-yl|orv)propyllamino}ethvl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{(2,2-dimethylpropyl)[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (350 mg, 0.45 mmol) yielded compound 11 in table 1 (325 mg, 100 % yield) :
'H-NMR (DMSO d6, TFA) : 8.94 (s, 1H), 8.3 (s, 1H), 7.63 (d, 1H), 7.36 (s, 1H), 7.34 (m, 2H), 6.88 (m, 1H), 6.82 (s, 1H), 4.30 (m, 4H), 3.99 (s, 3H), 3.84 (s, 2H), 3.54 (m, 2H), 3.38 (m, 2H), 3.19 (m, 2H), 2,37 (m, 2H), 1.09 (s, 9H) : MS (+ve ESI) : 660.4 (M+H)+.
di-/'er/-butyl2-{(2,2-dimethylpropyl)[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH'-pyrazol-3-yl)amino]-6-methoxyquiiiazolin-7-yl}oxy)propyl]amino}ethyl phosphate used as starting material was obtained as follows :
a) Ethylene oxide (2.5 ml, 5.0 mmol) cooled to —20 °C was slowly added to a solution of
(2,2-dimethylpropyl)amine (13 g, 150 mmol) in methanol (15 ml) at —30 °C under argon. The
mixture was stirred at ambient temperature for 16 hours. The solvent was evaporated in
vacua, and the residue was purified by distillation (b.p. 132°C / 9 mmHg) to yield 2-((2,2-
dimethylpropyl)amino)ethanol (6.4 g, 97 % yield) :
'H-NMR (DMSO d6, TFA): 3.70 (m, 2H), 3.02 (m, 2H), 2.81 (m, 2H), 0.98 (s, 9H).
b) An analogous reaction to that described in example 5a, but starting with 2-(2,2-
dimethylpropyl)amino)ethanol (203 mg, 1.55 mmol) yielded 2-{3-[(7-{3-[(2,2-
dimethylpropyl)(2-hydroxyemyl)airmio]propoxy}-6-memoxyquinazolm-4-yl)amino]-lH-
pyrazol-5-yl}-7V-(3-fluorophenyl)acetamide (111 mg, 61 % yield):
'H-NMR (DMSO dfi, TFA) : 8.96 (s, m), 8.30 (s, m), 7.64 (d, m), 7.32-7.41 (m, 2H), 7.34
(s, 1H), 6.90 (t, 1H), 6.83 (s, 1H), 4.31 (t, 2H), 3.99 (s, 3H), 3.84 (s, 2H), 3.83 (t, 2H), 3.42 (t, 2H), 3.32 (t, 2H), 3.20 (dd, 2H), 2.35 (m, 2H), 1.07 (s, 9H): MS (+ve ESI): 580.3 (M+H)+.
c) An analogous reaction to that described in example 5b, but starting with 2-{3-[(7-{3-
[(2,2-dimethylpropyl)(2-hydroxyemyl)amino]propoxy}-6-methoxyqumazolm^-yl)aaiino]-
l/f-pyrazol-5-yl}-7V"-(3-fluorophenyl)acetamide (1.33 g, 2.3 mmol) yielded di-tert-bntyl 2-
{(2,2-dimethylpropyl)[3
yl)amino]-6-methoxyquinazoliB-7-yl}oxy)propyl]amino}ethyl phosphate (620 mg, 40 %
yield) :
'H-NMR (DMSO d& TFA): 8.95 (s, 1H), 8.3 (s, 1H), 7.64 (d, 1H), 7.28-7.40 (m, 2H), 7.34
(s, IH), 6.88 (m, IH), 6.84 (s, IH), 4.31 (m, 4H), 4.00 (s, 3H), 3.85 (s, 2H), 3.56 (m, 2H),
3.39 (m, 2H), 3.21 (m, 2H), 2.32 (m, 2H), 1.43 (s, 9H ), 1.10 (s, 9H) :
MS (+ve ESI) : 716.4 (M+H)+.
Example 12 - Preparation of compound 12 in table 1 - l-F3-(l4-r(5-f2-rr3-fluorophenvl)aminol-2-oxoethvI}-lJ3r-pyrazoI-3-ynamino1-6-methoxyquinazolin-7-yI)oxy)propyl1piperidin-3-yl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl l-[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-l^-pyrazol-3-yl)amiao3-6-methoxyquinazolin-7-yl}oxy)propyl]piperidin-3-yl phosphate (540 mg, 0.72 mmol) yielded compound 12 in table 1 (500 mg, 98 % yield):
'H-NMR (DMSO d6, TFA) : 8.92 (s, m), 8.28 (s, m), 7.62 (d, m), 7.32 (m, SH), 6.82 (m,
2H), 4.45-4.66 (m, 2H), 4.27 (m, 2H), 3.99 (s, 3H), 3.84 (s, 2H), 3.55 (m, 2H), 3.30 (m, 2H),
3.00 (m, 2H), 2.30 (m, 2H), 2.05 (m, 2H), 1.65 (m, 2H):
MS (+ve ESI): 630.2 (M+H)+.
di-tert-butyl 1 -[3-( {4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)amino]-6-
methoxyquinazolin-7-yl}oxy)propyl]piperidin-3-yl phosphate used starting material was
obtained as follows :
a) An analogous reaction to that described in example 5a, but starting with piperidin-3-ol
(101 mg, 1 mmol) yielded7Vr-(3-fluorophenyl)-2-[3-({7-[3-(3-hydroxypiperidin-l-
yl)propoxy]-6-memoxyquinazolin-4-yl}aaiuio)-lJyr-pyrazol-5-yl]acetamide (65 mg, 47 %
yield) :
'H-NMR (DMSO d6, TFA) : 8.96 (s, m), 8.29 (s, IH), 7.62 (d, m), 7.38 (m, 2H), 7.34 (m,
2H), 7.34 (s, IH), 6.90 (m, IH), 6.84 (s, IH), 4.28 (m, 2H)5 4.10 (m, IH), 4.00 (s, 3H), 3.85 (s, 2H), 2.80-3.50 (m, 6H), 1.30-2.40 (m, 6H) : MS (+ve ESI): 550.6 (M+H)+.
b) An analogous reaction to that described in example 5b, but starting with 7V-(3-
fluorophenyl)-2-[3-({7-[3-(3-hydroxypiperidin-l-yl)propoxy]-6-methoxyqumazolin-4-
yl}ammo)-l#-pyrazol-5-yl]acetamide (604 mg, 1.1 nimol) yielded di-tert-butyl l-[3-({4-[(5-

{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquiiiazolii>7-
yl}oxy)propyl]piperidin-3-yl phosphate (550 mg, 67 % yield):
'H-NMR (DMSO d& TFA): 8.38 (s, IH), 7.90 (s, IH), 7.55 (d, IH), 7.30 (m, 2H), 7.06 (s,
IH), 6.80 (m, 2H), 4.09 (m, 3H), 3.86 (s, 3H), 3.68 (s, 2H), 2.80 (m, IH), 2.55 (m, IH), 2.03
(m, 2H), 1.87 (m, 3H), 1.60 (m, IH), 1.35 (m, 22H):
MS (+ve ESI): 742.5 (M+H)+.
Example 13 - Preparation of compound 13 in table 1 - {f2Jif)-l-r3-f|4-f(5-(2-f(2,3-difluorophenyl)amino1-2-03i:oethvl}-lfl-pvrazol-3-vl)amino1-6-methoxyquinazolin-7-vl]oxy)propyllpyrrolidm-2-yl}methvl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl {(2K)-1 -[3-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} -lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (445 mg, 0.59 mmol) yielded compound 13 in table 1 (440 mg, 94 % yield) :
'H-NMR (DMSO d6, TFA): 8.94 (s, IH), 8.31 (s, IH), 7.73 (m, IH), 7.40 (s, IH), 7.19 (m, 2H), 6.83 (s, IH), 4.31 (t, 2H), 4.20 (m, 2H), 4.01 (s, 3H), 3.94 (s, 2H), 3.82 (m, IH), 3.70 (m, IH), 3.60 (m, IH), 3.31 (m, IH), 3.23 (m, IH), 2.32 (m, 2H), 2.19 (m, IH), 2.04 (m, IH), 1.95(m, lH);1.85(m, IH): MS (+ve ESI): 648.3 (M+H)+.
di-tert-butyl {(2R)-1 -[3-( {4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidm-2-yl}methyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 6b, but starting with (2R)-
pyrrolidin-2-ylmethanol (101 mg, 1 mmol) yielded JV-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2^)-
2-(hydroxymethyl)pyn-olidin-l-yl]propoxy}-6-memoxyqumazolin-4-yl)aniino]-l^T-pyrazol-5-
yl}acetamide (134 mg, 79 % yield):
'H-NMR (DMSO d6, TFA) : 8.95 (s, m), 8.29 (s, m), 7.75 (m, m), 7.32 (s, m), 7.16 (m,
2H), 6.84 (s, IH), 4.30 (m, 2H), 4.00 (s, 3H), 3.94 (s, 2H), 3.70-3.85 (m, IH), 3.52-3.70 (m,
4H), 3.15-3.30 (m, 2H), 2.25-2.35 (m, 2H), 1.75-2.20 (m, 4H):
MS ES+: 568.2 (M+H)+
MS (+ve ESI) : 568.2 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with //-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(2/?)-2-(hydroxymethyl)pyrrolidm-l-yl]propoxy}-6-

methoxyquinazolin^-y^aminoJ-lF-pyrazol-S-ylJacetamide (1.1 g, 1.9 mtnol) yielded di-tert-butyl {(2R)-l-[3-({4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]pyrrolidia-2-yl}methyl phosphate (453 rag, 31 % yield):
'H-NMR (DMSO d6, TFA) : 10.24 (s, IH), 10.15 (s, IH), 8.44 (s, IH), 7.98 (s, m), 7.72 (t,
IH), 7.19 (m, 2H), 7.13 (s, IH), 6.83 (s, IH), 4.17 (br s, 2H), 3.93 (s, 3H), 3.85 (s, IH), 3.77
(m, IH), 3.56 (t, IH), 3.54 (t, IH), 3.08 (t, IH), 2.94 (m, IH), 2.66 (m, IH), 2.47 (m, IH),
2.20 (q, IH), 1.94 (m, 2H), 1.86 (m, IH), 1.69 (m, 2H), 1.60 (m, IH), 1.37 (s, 9H), 1.36 (s,
9H):
MS (+ve ESI) : 758.5 (M+H)"1".
Compound 13, synthesised above as the dihydrochloride salt, could also be prepared as the
free base according to the following method:
c) An analogous reaction to that described in example 6d, but starting with Compound 13
yielded the free base of Compound 13 as a pale yellow solid:
1H-NMR (DMSO d«) : 10.30 (s, IH), 10.20 (s, IH), 8.50 (s, IH), 8.00 (s, IH), 7.70-7.80 (m,
IH), 7.20-7.30 (m, 3H), 6.70 (s, IH), 4.30-4.40 (m, 2H), 4.10-4.20 (m, IH), 3.90 (s, 3H), 3.80
(s, 2H), 3.70-3.75 (m, IH), 3.40-3.50 (m, IH), 3.30-3.35 (in, IH), 3.20-3.25 (m, IH), 3.05-
3.15 (m, IH), 2.90-3.00 (m, IH), 2.10-2.20 (m, 2H), 1.90-2.00 (m, IH), 1.70-1.80 (m, 3H) :
MS (+ve ESI): 648 (M+H)+.
CasHs^NvOyP + 2.3H2O requires C, 48.8%; H, 5.35%; N, 14.23%; Found C, 48.95%; H,
5.03%; N, 14.15%
Example 14 - Preparation of compound 14 in table 1 - 2-fr3-(|4-r(5-|2-r(3,5-difluorophenvl)amino1-2-oxoethyl|-lfl-pyrazol-3-yl)amino1-6-methoxyquinazolin-7-vl}oxv)propylKprop-2-vn-l-yl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino3-2-oxoe%l}-l//-pyrazol-3-yl)aniino]-6-methoxyquinazolin-7-yl}oxy)propyl](prop-2-yn-l-yl)amino]ethyl phosphate (400 mg, 0.53 mmol) yielded compound 14 in table 1 (290 mg, 77 % yield):
'H-NMR (DMSO &, TFA) .- 8.94 (s, IH), 8.34 (s, IH), 7.42 (m, SH), 6.89 (m, 2H), 4.37 (m,
6H), 4.04 (s, 3H), 3.92 (s, 2H), 3.87 (s, IH), 3.57 (m, 2H), 3.47 (m, 2H), 2.39 (m, 2H) : MS (+ve ESI): 646.4 (M+H)+.

di-ter/-buty!2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)aminoJ-6-methoxyquinazolin-7-yl} oxy)propyl](prop-2-yn-1 -yl)amino]ethyl phosphate used as starting material was obtained as follows :
a) A cooled (-40 °C) solution of ethylene oxide (3.3 g, 75 mmol) in methanol (10 ml)
was slowly added to a solution of propargylamine (16.5 g, 300 mmol) in methanol (60 ml)
cooled to -65 ° C under argon. The mixture was allowed to warm to ambient temperature
over 16 hours, the solvent was evaporated in vacua, and the residue was purified by
distillation to yield 2-(prop-2-yn-l-ylamino)ethanol (5.0 g, 67 % yield) :
'H-NMR (OMSO d6, TEA): 3.91 (m, 2H), 3.65 (m, 3H), 3.06 (rn, 2H).
b) An analogous reaction to that described in example 8a, but starting with 2-(prop-2-yn-
l-ylamino)ethanol (99 mg, 1 mmol) and heating at 105 °C for 12 hours yielded 7V-(3,5-
difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(prop-2-yn-l-yl)amino]propoxy}-6-
methoxyquinazolm-4-yl)amino]-17y-pyrazol-5-yl}acetamide (50 mg, 31 % yield):
'H-NMR (DMSO d6, TFA) : 8.95 (s, m), 8.29 (s, m), 7.34 (m, 2H), 7.31 (s, m), 6.91 (m,
1H), 6.83 (s, 1H), 4.29 (m, 4H), 4.00 (s, 3H), 3.89 (m, 1H), 3.86 (s, 2H), 3.80 (m, 2H), 3.43 (m, 2H), 3.36 (m, 2H), 2.30 (m, 2H) : MS (+ve ESI) : 566.2 (M+H)+.
c) An analogous reaction to that described in example 8b, but starting with N-(3,5-
difluorophenyl)-2- {3 -[(7- {3-[(2-hydroxyethyl)(prop-2-yn-1 -yl)amino]propoxy} -6-
methoxyquinazolui-4-yl)amino]-lH-pyrazol-5-yl}acetamide (734 mg, 1.3 mmol) yielded di-
^^butyl2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)ammo]-2-oxoemyl}-m-pyrazol-3-yl)arnino]-
6-methoxyquinazolin-7-yl}oxy)propyl](prop-2-yn-l-yl)amino]ethyl phosphate (400 mg, 41 %
yield) :
'H-NMR (DMSO d Example 15 - Preparation of compound 15 in table 1 - 2-rr3-(|4-r(5-|2-[(2,3-difluorophenvl>amino1-2-oxoethyl>-lg-pvrazol-3-yl)amino1-6-methoxyquinazolin-7-yl}oxy)propynfisopropyl)amino1ethyl dihvdrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)arriino]-2-oxoe%l}-l^"-pyrazol-3-yl)amino]-6-

methoxyquinazolin-7-yl}oxy)propyl](isopropyl)amino]ethyl phosphate (450 mg, 0.59 mmol) yielded compound 15 in table 1 (405 mg, 95 % yield) :
'H-NMR (DMSO d6): 8.90 (s, m), 8.32 (s, IH), 7.69 (m, m), 7.51 (s, m), 7.21 (m, 2H),
6.81 (s, IH), 4.33 (m, 2H), 4.26 (m, 2H), 4.00 (s, 3H), 3.92 (s, 2H), 3.72 (m, IH), 3.40 (m, 2H), 3.29 (m, 2H), 2.32 (m, 2H), 1.31 (m, 6H): MS (+ve ESI): 650.3 (M+H)+.
di-re^butyl2-[[3 a) An analogous reaction to that described in example 6b, but starting with 2-
(isopropylamino)ethanol (103 mg, 1 mmol) yielded JV-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyemyl)(isopropyl)atnino]propoxy}-6-methoxyquina2olm-4-yl)amino]-l/;f-pyrazol-5-
yl}acetamide (84 mg, 49 % yield) :
]H-NMR (DMSO d6, TFA): 8.97 (s, IH), 8.33 (s, IH), 7.79 (m, IH), 7.35 (s, IH), 7.18 (m, 2H), 6.88 (s, IH), 4.34 (t, 2H), 4.03 (s, 3H), 3.98 (s, 2H), 3.81 (m, 3H), 3.40 (m, 3H), 3.20 (m, IH), 2.35 (m, 2H), 1.33 (m, 6H) : MS (+ve ESI) : 570.2 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 7V-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(isopropyl)amino]propoxy}-6-
methoxyquinazolm-4-yl)amino]-lJ:/'-pyrazol-5-yl}acetamide (650 mg, 1.14 mmol) yielded di-
/er^butyl2-[[3 6-methoxyquinazolin-7-yl}oxy)propyl](isopropyl)amino]ethyl phosphate (520 mg, 60 %
yield):
'H-NMR (DMSO d6).- 8.44 (s, m), 7.98 (s, m), 7.73 (m, m), 7.19 (m, 2H), 7.12 (s, IH),
6.83 (s, IH), 4.16 (t, 2H), 3.93 (s, 3H), 3.85 (s, 2H), 3.77 (m, 2H), 2.90 (m, IH), 2.60 (m, 4H), 1.86 (m, 2H), 1.36 (s, 18H), 0.94 (m, 6H) : MS (+ve ESI) : 762.7 (M+H)+.
Example 16 - Preparation of compound 16 in table 1 - 2-ff3-(|4-f(5-(2-r(2,3-difluorophenyI)amino1-2-oxoethyU-ljy-pyrazol-3-yl)amino1-6-methoxyquinazoIin-7-yl}oxy)propyl1(prop-2-yn-l-yl)aminolethyIdihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-/er/-butyl 2-[[3
methoxyquina2olin-7-yl}oxy)propyl](prop-2-yn-l-yl)aniino]ethyl phosphate (630 mg, 0.84 mmol) yielded compound 16 in table 1 ((540 mg, 86 % yield) :
'H-NMR (DMSO d6, AcOD): 8.89 (s, 1H), 8.29 (m, 1H), 7.70 (m, 1H), 7.37 (m, 1H), 7.16 (m, 2H), 6.81 (m, 1H), 4.29 (m, 6H), 3.99 (m, 3H)3 3.92 (m, 2H), 3.82 (m, 1H), 3.52 (m, 2H), 3.43 (m, 2H), 2.32 (m, 2H) : MS (+ve ESI): 646.3 (M+H)+.
di-fer/-butyl2-[[3-({4-[(5-{2-[(253-difluorophenyl)amino]-2-oxoethyl}-l//-pyrazol-3-yl)amko]-6-methoxyquinazolin-7-yl}oxy)propyl](prop-2-yn-l-yl)amino]ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 6b, but starting with 2-(prop-2-yn-
l-ylamino)ethanol (99 mg, 1 mmol) yielded Af-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyethyl)(prop-2-yn-1 -yl)amino]propoxy} -6-methoxyquinazolin-4-yl)amino]- IH-
pyrazol-5-yl}acetamide (128 mg, 75 % yield) :
'H-NMR (DMSO d6, TFA) : 8.95 (s, m), 8.29 (s, m), 7.74 (m, IH), 7.31 (s, m), 7.18 (m,
2H), 6.83 (s, IH), 4.30 (m, 4H), 4.00 (s, 3H)5 3.94 (s, 2H), 3.87 (m, IH), 3.80 (m, 2H), 3.44 (m, 2H), 3.35 (m, 2H), 2.30 (m, 2H) : MS (+ve ESI): 566.2 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with N-(2,3-
difluorophenyl)-2- {3 -[(7- {3-[(2-hydroxyethyl)(prop-2-yn-1 -yl)amino]propoxy} -6-
methoxyquinazolm-4-yl)amino]-lfl'-pyrazol-5-yl}acetamide (680 mg, 1.2 mmol) yielded di-
te^butyl 2-[[3-({4-[(5-{2-[(2,3-difluoropheny^
6-methoxyqumazolin-7-yl}oxy)propyl](prop-2-yn-l-yl)amino]ethyl phosphate (630 mg, 70 % yield):
1H-NMR (DMSO d6) : 8.45 (s, IH), 7.98 (s, IH), 7.72 (m, IH), 7.17 (m, 3H), 6.83 (s, IH),
4.16 (m, 2H)3 3.85 (m, 7H), 3.45 (m, 2H), 3.13 (m, IH), 2.69 (m, 4H), 1.90 (m, 2H), 1.35 (m,
18H):
MS (+ve ESI): 758.5 (M+H)+.
Example 17 - Preparation of compound 17 in table 1 - 2-f [3-((4-f(5-|2-[(2,3-difluorophenvl)aminol-2-oxoethyl}-ljy-pyrazoI-3-vl)amino]-6-methQxyquinazolin-7-yl|oxy)propvn(2-methoxyethyl)amino^ethyl dihvdrogen phosphate
An analogous reaction to that described in example 1, but starting with di-ter/-butyl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)ainino]-2-oxoethyl}-l^f-pyrazol-3-yl)amino]-6-

methoxyquinazolin-7-yl}oxy)propyl](2-methoxyethyl)ainino]ethyl phosphate (500 mg, 0.64 mmol) yielded compound 17 in table 1 (450 mg, 94 % yield) :
'H-NMR (DMSO d6, AcOD): 8.91 (s, IH), 8.33 (s, IH), 7.74 (m, IH), 7.43 (s, IH), 7.18 (m, 2H)5 6.85 (s, IH), 4.32 (m, 4H), 4.02 (s, 3H), 3.96 (s, 2H), 3.77 (m, 2H), 3.56 (m, 2H), 3.49 (m, 2H), 3.44 (m, 2H), 3.34 (s, 3H), 2.34 (m, 2H): MS (+ve ESI): 666.2 (M+H)+.
di-to"r-butyl2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lJ¥-pyrazol-3-yl)anaino]-6-methoxyquinazolin-7-yl}oxy)propyl](2-methoxyethyl)amino]ethyl phosphate used as starting material was obtained as follows:
a) An analogous reaction to that described in example 6b, but starting with 2-((2-
methoxyethyl)amino)ethanol (119 mg, 1 mmol - prepared according to A.A. Santilli et al, J.
Heterocycl. Chem. 1972, 9, 309-13) yielded JY-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyettiyl)(2-methoxyemyl)ammo]propoxy}-6-memoxyqumazolm-4-yl)aminoJ-lJcZ-
pyrazol-5-yl}acetamide (124 mg, 71 % yield) :
'H-NMR (DMSO d6, TFA): 8.97 (s, IH), 8.31 (s, IH), 7.76 (m, IH), 7.33 (s, IH), 7.19 (m, 2H), 6.85 (s, IH), 4.31 (t, 2H), 4.02 (s, 3H), 3.95 (s, 2H), 3.80 (t, 2H), 3.73 (t, 2H), 3.45 (m, 4H), 3.36 (m, 5H), 2.31 (m, 2H) : MS (+ve ESI): 586.2 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 7V-(2,3-
difluorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(2-methoxyethyl)amino]propoxy} -6-
methoxyquinazolin-4-yl)amino]-lJf/-pyrazol-5-yl}acetamide (800 mg, 1.4 mmol) yielded di-
^^butyl2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoe%l}4ff-pyrazol-3-yl)amino]-
6-methoxyquinazolin-7-yl}oxy)propyl](2-methoxyethyl)amuio]ethyl phosphate (560 mg, 53
% yield) :
'H-NMR (DMSO d6): 8.44 (s, IH), 7.99 (s, IH), 7.72 (m, IH), 7.20 (m, 2H), 7.12 (s, IH), 6.84 (s, IH), 4.16 (t, 2H), 3.93 (t, 3H), 3.85 (m, 4H), 3.38 (m, 2H), 3.20 (s, 3H), 2.74 (m, 2H), 2.67 (m, 4H), 1.90 (m, 2H), 1.39 (m, 18H): MS (+ve ESI): 778.6 (M+H)+.
Example 18 - Preparation of compound 18 in table 1 - 2-(f3-fl4-r(5-l2-r(3-fluorophenyl)amino1-2-oxoethvl>-lH-pvrazol-3-yl)amino1-6-methoxyquinazoIin-7-yl}oxy)propyl|aminotethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoe%l}-l^-pyra2ol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl phosphate (729 mg, 1.04 mmol) yielded compound 18 in table 1 (505 mg, 72 % yield):
'H-NMR (DMSO de, AcOD) : 8.85 (s, 1H), 8.25 (s, 1H), 7.60 (d, 1H), 7.33 (m, 3H), 6.83 (m, 1H), 6.80 (s, 1H), 4.27 (m, 2H), 4.15 (m, 2H), 3.97 (s, 3H), 3.83 (s, 2H), 3.26 (m, 2H), 3.15 (m, 2H), 2.24 (m, 2H): MS (+ve ESI) : 590.1 (M+H)+.
di-fe;^butyl2-{[3 a) An analogous reaction to that described in example 5a, but starting with 2-
(cyclopropylamino)ethanol (156 mg, 1.55 mmol) yielded 2-{3-[(7-{3-[cyclopropyl(2-
hydroxyemyl)aniino]propoxy}-6-memoxyquinazoh^^-yl)amino]-lH-pyrazol-5-yl}-7V'-(3-
fluorophenyl)acetamide (22 mg, 13 % yield):
'H-NMR (DMSO d6, TFA) : 8.97 (s, m), 8.31 (s, m), 7.65 (d, m), 7.33-7.42 (m, 2H), 7.37
(s, 1H), 6.92 (t, 1H), 6.85 (s, 1H), 4.33 (m, 2H), 4.02 (s, 3H), 3.86 (s, 2H), 3.79 (t, 2H), 3.48 (m, 2H), 3.42 (t, 2H), 2.97 (m, 1H), 2.36 (m, 2H), 1.04 (m, 2H), 0.94 (m, 2H) : MS (+ve ESI) : 550.2 (M+H)+.
b) An analogous reaction to that described in example 5b, but starting with 2-{3-[(7-{3-
[cyclopropyl(2-hydroxyemyl)animo]propoxy}-6-me1hoxyquinazolin-4-yl)amino]-lJ:r-
pyrazol-5-yl}-JV-(3-fluorophenyl)acetamide (1.1 g, 2.0 mmol) yielded a mixture of di-tert-
butyl 2-{cyclopropyl[3-({4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-
yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (150 mg, 10 %
yield) together with di-ter/-butyl 2-{[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-17?-
pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (730 mg,
52 % yield) which was used in the next step :
'H-NMR (DMSO d6, TFA): 8.97 (s, 1H), 8.32 (s, 1H), 7.78 (d, 1H), 7.36 (rn, 2H), 7.34 (s, 1H), 6.87 (m, 2H), 4.33 (in, 2H), 4.16 (m, 2H), 4.03 (s, 3H), 3.88 (s, 2H), 3.33 (m, 2H), 3.24 (m, 2H), 2.38 (m, 2H), 1.47 (s, 18H):
MS (+ve ESI) : 702.5 (M+H)+.
Example 19 - Preparation of compound 19 in table 1 - 2-((cvcIobutYlmethyl)r3-f{4-f(5-(2-[(2,3-difluorophenyl)amino1-2-oxoethyl}-lJgr-pvra2ol-3-yl)aminol-6-methoxyquinazolin-V-yUoxylpropynaminolethyldihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-bntyl 2-
yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (400 mg, 0.508 mmol) yielded compound 19 in table 1 (365 mg, 96 % yield) :
!H-NMR (DMSO d& AcOD) : 8.92 (s, 1H), 8.33 (s, 1H), 7.71 (m, 1H), 7.44 (s, 1H), 7.19 (m, 2H), 6.82 (s, 1H), 4.30 (m, 4H), 4.00 (s, 3H), 3.94 (s, 2H), 3.42 (m, 2H), 3.29 (m, 4H), 2.82 (m, 1H), 2.31 (m, 2H), 2.13 (m, 2H), 1.87 (m, 4H) : MS (+ve ESI) : 676.4 (M+H)+.
di-fe/^buty!2-{(cyclobutyhiie%l)[3K{4-[(5-{2-[(23-difluorophenyl)amino]-2-oxoethyl}-l#-pyrazol-3-yl)ammo]-6-methoxyqumazolin-7-yl} oxy)propyl]amino} ethyl phosphate used as starting material was obtained as follows :
a) Cyclobutane carbonyl chloride (5 ml, 43.8 mmol) was slowly added to a solution of
ethyl glycinate (5.86 g, 42 mmol) in dichloromethane (100 ml) and triethylamine (14.6 ml,
105 mmol) at 0 °C. The mixture was then stirred at ambient temperature for 14 hours. The
reaction mixture was washed with a dilute hydrochloric acid (1.0 N), the organic phase was
separated, dried and evaporated in vacua to give a yellow solid. Recrystallisation from
dichloromethane / petroleum ether yielded ethyl N-(cyclobutylcarbonyl)glycinate as a white
solid (7.78 g, 100 % yield) :
'H-NMR (DMSO d6) : 8.08 (t, 1H), 4.09 (q, 2H), 3.79 (s, 2H), 3.07 (m, 1H), 2.00-2.18 (m, 4H), 1.89 (m, 1H), 1.78 (m, 1H), 1.20 (t, 3H).
b) Ethyl N-(cyclobutylcarbonyl) glycinate (7.6 g, 41 mmol) in tetrahydrofuran (40 ml)
was added to a solution of diborane (100 ml of a 1.0 N solution in tetrahydrofuran, 100 mmol)
and heated at 60 °C for 24 hours. Additional diborane (20 ml of a 1.0 N solution in
tetrahydrofuran, 20 mmol) was added to the mixture and heating was carried out for a further
8 hours. Methanol (20 ml) was added cautiously and the reaction stirred for 30 minutes at
ambient temperature before slow addition of hydrochloric acid (6 ml of a 6.0 N solution). The
reaction was concentrated in vacua, dichloromethane was added and the solid material
removed by suction filtration. The organic filtrate was dried, concentrated in vacua and
purified by chromatography on silica gel, eluting with dichloromethane / methanol (96:4) to dichloromethane / methanol / ammonia (7.0N) (94:5:1) to yield 2-((cyclobutyhnethyl)amino)ethanol (4.16 g, 78 % yield) :
'H-NMR (DMSO d6) TFA) : 8.38 (br s, IH), 3.65 (t, 2H), 2.98 (m, 4H), 2.62 (m, 2H), 2.06 : (m,2H), 1.72-1.94 (m,4H).
c) An analogous reaction to that described in example 6b, but starting with 2-
((cyclobutylmethyl)amino)ethanol (129 mg, 1 mmol) yielded 2-{3-[(7-{3-
[(cyclobutymiethyl)(2-hydroxyemyl)ammo]propoxy}-6-methoxyqumazolm-4-yl)amino]-17:f-
pyrazol-5-yl}-JV-(2,3-difluorophenyl)acetamide (134 mg, 75 % yield):
'H-NMR (DMSO d6): 8.49 (s, m), s.oo (s, IH), 7.74 (m, m), 7.15-7.30 (m, SH), 6.75 (m,
IH), 4.25 (m, 2H), 3.96 (s, 3H), 3.86 (s, 2H), 3.60-3.80 (m, 2H), 3.30-3.40 (m, 4H), 2.50-2.80 (m,4H), 1.60-2.40 (m,7H): MS (+ve ESI) : 596.2 (M+H)+.
d) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
[(cyclobutylmethyl)(2-hydroxyethyl)amino]propoxy} -6-memoxyqiunazolm-4-yl)amino] - \H-
pyrazol-5-yl}-7Y-(2,3-difluorophenyl)acetamide (773 mg, 1.3 mmol) yielded di-tert-butyl 2-
{(cyclobutylmethyl)[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l//'-pyra2ol-3-
yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (400 mg, 40 %
yield):
]H-NMR (DMSO d6) : 8.45 (s, IH), 7.99 (s, IH), 7.72 (m, IH), 7.20 (m, 3H), 6.83 (s, IH), 4.15 (s, 2H), 3.94 (s, 3H), 3.85 (m, 4H), 2.60 (m, 4H), 2.47 (m, 3H), 1.88 (rn, 4H), 1.75 (m, 2H), 1.60 (m, 2H), 1.36 (s, 18H): MS (+ve ESI): 788.8 (M+H)+.
Example 20 - Preparation of compound 20 in table 1 - 2-ff3-(f4-rr5-{2-ff3-fluorophenvl)amino1-2-oxoethyI}-lg-pyra2oI-3-vl)amino1-6-methoxvquinazolin-7-yl|oxv)propyn(3,3,3-trifluoropropyl)amino1 ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-to-f-butyl 2-[[3-({4-[(5-{2-[(3-fluorophenyl)arriino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-memoxyqumazolm-7-yl}oxy)propyl](3,3)3-trifluoropropyl)arnino]ethyl phosphate (450 mg, 0.56 mmol) yielded compound 20 in table 1 (405 mg, 46 % yield) :
'H-NMR (DMSO A6, TFA): 8.95 (s, IE), 8.32 (s, 1H), 7.65 (d, 1H), 7.39 (s, 1H), 7.36 (m,
1H), 6.89 (m, 1H), 6.83 (s, 1H), 4.31 (t, 2H), 4.27 (m, 2H), 4.01 (s, 2H), 3.86 (s, 2H), 3.57 (br
s, 2H), 3.54 (m, 2H), 3.43 (t, 2H), 2.97 (m, 2H), 2.33 (m, 2H) :
MS (+ve ESI) : 686.4 (M+H)+.
di-fe^butyl 2-[[3-( {4-[(5-{2-[(3-fluorophen^
6-me1lioxyquinazolin-7-yl}oxy)propyl](3333-trifluoropropyl)arnino]ethyl phosphate used as
starting material was obtained as follows :
a) A solution of 3-bromo-l,l,l-rrifluoropropane (5.5 ml, 51.6 mmol) in dioxane (50 ml)
was heated with ethanol amine (3 ml, 51.25 mmol) at 60 °C for 36 hours in the presence of
potassium carbonate (14.2 g, 102 mmol). The solvent was evaporated in vacuo and the residue
was purified by chrornatography on silica gel, eluting with dichloromethane / methanol (95:5)
to dichloromethane /methanol / ammonia (7.0 N) (95:5:1) to yield 2-((3,3,3-
trifluoropropyl)amino)ethanol (4.47 g, 55 % yield) :
'H-NMR (DMSO d6, TFA) : 3.56 (t, 2H), 2.97 (t, 2H), 2.82 (t, 2H), 2.57 (m, 2H).
b) An analogous reaction to that described in example 5a, but starting with 2-((3,3,3-
trifluoropropyl)amino)ethanol (221 mg, 1.55 mmol) yielded 7V-(3-fluorophenyl)-2-{3-[(7-{3-
[(2-hydroxyethyl)(3,3,3-trifluoropropyl)amino]propoxy} -6-methoxyquinazolin-4-yl)arnino]-
l#-pyrazol-5-yl}acetarnide (77 mg, 41 % yield):
3H-NMR (DMSO d& TFA) : 8.96 (s, 1H), 8.29 (s, 1H), 7.63 (d, 1H), 7.31-7.40 (m, 2H), 7.33 (s, 1H), 6.89 (t, 1H), 6.83 (s, 1H), 4.29 (t, 2H), 3.99 (s, 3H), 3.84 (s, 2H), 3.79 (t, 2H), 3.51 (m, 2H), 3.38 (m, 2H), 2.91 (m, 2H), 2.29 (m, 2H) : MS (+ve ESI) : 606.2 (M+H)+.
c) An analogous reaction to that described in example 5b, but starting with N-(3-
fiuorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(3,3,3-trifluoropropyl)amino]propoxy} -6-
memoxyqumazolm-4~yl)arruno]-l#-pyrazol-5-yl}acetaniide (651 mg, 1.07 mmol) yielded di-
tert-butyl 2-[[3-( {4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-yl)amino]-6-
mefhoxyqumazolin-7-yl}oxy)propyl](3,3,3-trifluoropropyl)arnino]ethyl phosphate (455 mg,
53 % yield):
'H-NMR (DMSO d6): 10.45 (s, m), 10.15 (s, m), 8.44 (s, m), 7.98 (s, m), 7.62 (d, m),
7.35 (m, 1H), 7.33 (s, 1H), 7.13 (s, 1H), 6.89 (t, 1H), 6.82 (s, 1H), 4.16 (t, 2H), 3.93 (s, 3H),
3.87 (q, 2H), 3.76 (s, 2H), 2.73 (m, 4H), 2.66 (t, 2H), 2.42 (m, 2H), 1.90 (m, 2H), 1.37 (s,
18H):
MS (+ve ESI): 797.9 (M+H)+.
Example 21 - Preparation of compound 21 in table 1 - 2-|allyir3-fl4-rf5-(2-f('2.3-difluorophenyI)amino1-2-oxoethvl)-lg-pyrazol-3-Yl)amino1-6-methoxyquinazolm-7-vl}oxv)propyl1amino|ethvl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with 2-{allyl[3-({4-[(5-{2-[(23-difluorophenyl)arnino]-2-oxoethyl}-lJ:r-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl di-tert-butyl phosphate (310 mg, 0.408 mmol) yielded compound 21 in table 1 (293 mg, 100 % yield) :
'H-NMR (DMSO d6> AcOD) : 8.92 (s, 1H), 8.32 (s, 1H), 7.70 (m, 1H), 7.43 (s, 1H), 7.19 (m, 2H), 6.82 (s, 1H), 6.05 (m, 1H), 5.63 (m, 1H), 5.56 (m, 1H), 4.30 (m, 4H), 4.00 (s, 3H), 3.93 (m, 4H), 3.45 (m, 2H), 3.33 (m, 2H), 2.33 (m, 2H): MS (+ve ESI): 648.3 (M+H)+.
2-{allyl[3-({4-[(5-{2-[(23-difluorophenyl)ammo]-2-oxoethyl}-lJY-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl di-ter/-butyl phosphate used as starting material was obtained as follows:
a) Ethylene oxide (2.5 ml, 50 mmol - cooled to -20 °C) was added to a solution of
allylamine (14 g, 250 mmol) in methanol (20 ml) at —20 °C. The mixture was stirred at
ambient temperature for 14 hours, the solvent was evaporated in vacua and the residual oil
was purified by distillation (b.p. 140 °C / 14 mmHg) to yield 2-(allylamino)ethanol (4.2 g, 84
% yield):
'H-NMR (DMSO d6): 5.83 (m, 1H), 5.14 (m, 1H), 5.02 (m, 1H), 3.43 (m, 2H), 3.14 (m, 2H), 2.50 (m, 2H).
b) An analogous reaction to that described in example 6b, but starting with 2-
(allylammo)ethanol (101 mg, 1 mmol) yielded 2-{3-[(7-{3-[allyl(2-
hydroxyemyl)amino]propoxy}-6-methoxyqumazolm-4-yl)ammo]-lH-pyrazol-5-yl}-7V-(2,3-difluorophenyl)acetamide (99 mg, 58 % yield) :
'H-NMR (DMSO d6, TFA) : 8.97 (s, m), 8.32 (s, m), 7.77 (m, m), 7.33 (s, m), 7.is (m,
2H), 6.87 (s, 1H), 6.01 (m, 1H), 5.60 (m, 2H), 4.31 (t, 2H), 4.02 (s, 3H), 3.94 (m, 4H), 3.82 (t, 2H), 3.35 (m, 4H), 2.34 (m, 2H) : MS (+ve ESI): 568.2 (M+H)+.
c) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
[allyl(2-hydroxyethyl)amino]propoxy} -6-memoxyqumazolin-4-yl)amino]- lff-pyrazol-5-yl} -
J/V-(253-difluorophenyl)acetamide (1.0 g, 1.76 mmol) yielded 2-{allyl[3-({4-[(5-{2-[(2,3-
difluorophenyl)amiiio]-2-oxoethyl}-lfr-pyrazol-3-yl)animo]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl di-tert-butyl phosphate (310 nig, 23 % yield) :
'H-NMR (DMSO &, TFA) : 8.97 (a, IH), 8.30 (S, m), 7.75 (m, m), 7.32 (s, m), 7.20 (m,
2H), 6.85 (s, IH), 6.00 (m, IH), 5.74 (m, 2H), 4.30 (m, 4H), 4.01 (s, 3H), 3.95 (m, 4H), 3.50 (m, 2H), 3.37 (m, 2H), 2.30 (m, 2H), 1.45 (s, 18H): MS (+ve ESI) : 760.5 (M+H)+.
Example 22 - Preparation of compound 22 in table 1 - 2-|cycIobutyir3-({4-r(5-|2-r(2,3-difluorophenyl)amino1-2-oxoethyl}-Lg-pyrazol-3-yl)amino1-6-methoxyquinazolin-7-yl}oxy)propyl1amino}ethvl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{cyclobutyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (450 mg, 0.58 mmol) yielded compound 22 in table 1 (420 mg, 98 % yield) :
'H-NMR (DMSO d6, AcOD): 8.91 (s, IH), 8.31 (s, IH), 7.72 (m, IH), 7.42 (s, IH), 7.20 (m, 2H), 6.82 (s, IH), 4.28 (m, 4H), 4.00 (s, 3H), 3.94 (s, 3H), 3.35 (m, 2H), 3.25 (m, 2H), 2.41 (m, 2H), 2.25 (m, 4H), 1.70 (m, 2H): MS (+ve ESI): 662.5 (M+H)+.
di-/ert-butyl2-{cyclobutyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amuio]-2-oxoethyl}-lH-pyrazol-3-yl)ammo]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 6b, but starting with 2-
(cyclobutylamino)ethanol (117 mg, 1 mmol — prepared according to D.F. Morrow et al, J.
Med Chem. 1973,16, 736-9.) and potassium iodide (103 mg, 0.62 mmol) in
dimethylacetamide (2 ml) at 95 °C for 4 hours under argon yielded 2-{3-[(7-{3-[cyclobutyl(2-
hydroxyethyl)amino]propoxy} -6-methoxyquinazolin-4-yl)amino]- lH-pyrazol-5-yl} -N-(2,3-
difluorophenyl)acetamide (97 mg, 56 % yield) :
'H-NMR (DMSO d6, TFA) : 8.92 (s, m), 8.27 (s, IH), 7.74 (m, IH), 7.29 (s, IH), 7.15-7.20
(m, 2H), 6.83 (s, IH), 4.30 (m, 2H), 3.98 (s, 3H), 3.98 (m, 3H), 3.68-3.80 (m, 2H), 3.20-3.30 (m, 2H), 3.15 (m, 2H), 2.30 (m, 2H), 2.22 (m, 4H), 1.65-1.82 (m, 2H) : MS (+ve ESI): 582.2 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
[cyclobutyl(2-hydroxyethyl)anuno]propoxy}-6-methoxyqumazolm-4-yl)amino]-lH-pyrazol-
5-yl}-jV-(2,3-difluorophenyl)acetamide (668 mg, 1.15 mmol) yielded di-fer^-butyl 2-{cyclobutyl[3-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} - l/f-pyrazol-3 -yl)amino]-6-memoxyquinazoLin-7-yl}oxy)propyl]amino} ethyl phosphate (450 mg, 51 % yield): 'H-NMR (DMSO d6) : 8.44 (s, IH), 7.98 (s, 1H), 7.70 (m, IH), 7.18 (m, 3H), 6.83 (s, 1H), 4.15 (t, 2H), 3.90 (s, 3H)5 3.85 (m, 4H), 3.15 (m, 1H), 2.62 (m, 4H), 1.90 (m, 4H), 1.75 (m, 2H), 1.53 (m, 2H), 1.39 (s, 18H) : MS (+ve ESI) : 774.8 (M+H)+.
Example 23 - Preparation of compound 23 in table 1 - 2-{cyclopentylf3-(|4-[f5-|2-r(2,3-difluorophenvl)amino1-2-oxoethyI}-lg-pyrazol-3-yI)amino1-6-methoxyquinazolin-7-yl}oxv)propyl1amino}ethyl dihydrogen phosphate
An analogous reaction to that described hi example 1, but starting with di-tert-butyl 2-{cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)aromo]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (360 mg, 0.46 mmol) yielded compound 23 hi table 1 (330 mg, 95 % yield) :
'H-NMR (DMSO d6) ACOD) : 8.91 (s, IH), 8.32 (s, m), 7.70 (m, IH), 7.43 (s, m), 7.20 (m,
2H), 6.82 (s, IH), 4.31 (m, 4H), 4.00 (s, 3H), 3.94 (s, 2H), 3.80 (m, IH), 3.48 (m, 2H), 3.36
(m, 2H), 2.33 (m, 2H), 2.08 (m, 2H), 1.75 (m, 4H), 1.58 (m, 2H) :
MS (+ve ESI) : 676.5 (M+H)+.
di-/ert-butyl 2- {cyclopentyl[3-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} - 1H-
pyrazol-3-yl)amhao]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl phosphate used as
starting material was obtained as follows :
a) An analogous reaction to that described in example 6b, but starting with 2-
(cyclopentylamino)ethanol (129 mg, 1 mmol - prepared according to D.F. Morrow et al. J.
Med. Chem. 1973,16, 736-9.) yielded 2-{3-[(7-{3-[cyclopentyl(2-
hydroxyethyl)amino]propoxy} -6-methoxyquinazolm-4-yl)amino]- l/Z-pyrazol-5-yl} -N-(2,3-difluorophenyl)acetamide (86 mg, 48 % yield):
'H-NMR (DMSO d& TFA) : 8.93 (s, m), 8.28 (s, m), 7.73 (m, m), 7.30 (s, m), 7.14 (m,
2H), 6.83 (s, IH), 4.29 (m, 2H), 3.98 (s, 3H), 3.93 (s, 2H), 3.78 (m, 3H), 3.37 (m, 2H), 3.26 (m, 2H), 2.30 (m, 2H), 2.09 (m, 2H), 1.74 (m, 4H), 1.72 (m} 2H) : MS (+ve ESI) : 596.2 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
[cyclopentyl(2-hydroxyemyl)anuno]propoxy}-6-memoxyqumazolin-4-yl)amino]-lff-pyrazol-

5-yl}-jV-(2,3-difluorophenyl)acetamide (654 mg, 1.1 mrnol) yielded di-tert-bntyl 2-(cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amiiio]-2-oxoethyl}-lf£'-pyrazol-3-yl)aniinoJ-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (364 mg, 42 % yield) :
'H-NMR (DMSO d6).- 8.44 (s, m), 7.99 (s, m), 7.70 (m, IH), 7.18 (m, SH ), 6.83 (s, m),
4.15 (m, 2H), 3.90 (s, 3H), 3.83 (m, 4H), 3.07 (m, IH), 2.68 (m, 4H), 1.90 (m, 2H), 1.72 (m, 2H), 1.55 (m, 2H), 1.48 (m, 2H), 1.35 (m, 20H): MS (+ve ESI) : 789.0 (M+H)+.
Example 24 - Preparation of compound 24 in table 1 - 2-{cyclopropylf3-(|4-f(5-|2-f(3-fluorophenyl)aminQl-2-oxoethyI}-lg-pyrazol-3-yl)aminol-6-methoxyquinazolin-7-yI|oxv)propyI1amino} ethyl dihydrogen phosphate
Hydrochloric acid (1.05 ml of a 4.0 N solution in dioxane, 4.2 mmol) was added to a stirred suspension of di-tert-butyl 2-{cyclopropyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl} - l^f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]amino) ethyl phosphate (519 mg, 0.7 mmol) in dichloromethane (15 ml) and dioxane (30 ml) and the reaction stirred for 7 hours at 45 °C. The precipitate was recovered by suction filtration, the residue taken up in dichloromethane / methanol (8:2) and the solid material removed by filtration. The organic filtrate was evaporated in vacua and the residue triturated with diethyl ether to yield compound 24 in table 1 (430 mg, 88 % yield) :
'H-NMR (DMSO d6, ACOH) : 8.91 (s, m), 8.32 (s, m), 7.64 (m, m), 7.39 (m, 3H), 6.90
(m, IH), 6.80 (s, IH), 4.32 (m, 4H), 4.00 (s, 3H), 3.87 (s, 2H), 3.57 (m, 2H), 3.48 (m, 2H),
2.95 (m, IH), 2.40 (m, 2H), 1.18 (m, 2H), 0.92 (m, 2H) :
MS (+ve ESI) : 630.4 (M+H)+.
di-fer/-butyl2-{cyclopropyl[3-({4-[(5-{2-[(3-fJuorophenyl)amino]-2-oxoethyl}-lH-pyrazol-
3-yl)amino]-6-methoxyquinazolui-7-yl}oxy)propyl]amino} ethyl phosphate used as starling
material was obtained as follows :
a) Di-ter/-butyl-diemylphosphoramidite (523 ul, 2.1 mmol) was added within 5 minutes
to a solution of 2-{3-[(7-{3-[cyclopropyl(2-hydroxyethyl)amino]propoxy}-6-
memoxyqumazolm-4-yl)amino]-17:/-pyrazol-5-yl}-A'-(3-fluorophenyl)acetarnide (793 mg, 1.4
mmol) in dimethylformamide (8 ml) in the presence of tetrazole (245 mg, 3.5 mmol) at
ambient temperature under argon and the mixture was stirred for 1.5 hours.
The solution was cooled to 5 °C, cumene hydroperoxide (426 mg, 2.8 mmol) was slowly
added, and the mixture stirred at 50 °C for 1 hour and at ambient temperature for a further 1

hour. The mixture was cooled to 5 °C and triethyl phosphite (415 mg, 2.5 mmol) was added and the reaction stirred at ambient temperature for 1 hour. The solution was diluted with water, extracted with ethyl acetate and the organic phase was separated, dried and concentrated. The resultant oil was purified by chromatography on silica gel, eluting with dichloromethane / methanol (98:2) to dichloromethane / methanol / ammonia (7.0 N) (95:5:1), to give di-tert-bntyl 2-{cyclopropyl[3-({4-[(5-{2-[(3-fluorophenyl)amuio]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-6-methoxyquinazoHn-7-yl}oxy)propyl]arnino}ethyl phosphate as an off-white solid (630 mg, 59 % yield) :
'H-NMR (DMSO d6, TFA) : 8.97 (s, m), 8.32 (s, m), 7.55 (d, IH), 7.35 (m, 3H), 6.86 (m,
2H), 4.33 (m, 4H), 4.03 (s, 3H), 3.87 (s, 2H), 3.66 (m, 2H), 3.53 (m, 2H), 3.00 (m, IH), 2.38 (m, 2H), 1.45 (s, 18H), 1.07 (m, 2H), 0.96 (m, 2H) : MS (+ve ESI) : 759.7 (M+H)+.
Example 25 - Preparation of compound 25 in table 1 - 2-|(cycIopropylinethyl)r3-('{4-ff5-{2-f(2,3-difluorophenyI)amino]-2-oxoethyl}-lj8r-pvrazol-3-yI)aminol-6-methoxyquinazolin-7-yUoxy)propyl1amino)ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{(cyclopropylmethyl)[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^:-pyrazol-3-yl)ammo]-6-methoxyquinazolm-7-yl}oxy)propyl]amino} ethyl phosphate (725 mg, 0.94 mmol) yielded compound 25 in table 1 (661 mg, 90 % yield) :
]H-NMR (DMSO d6, TFA): 8.95 (s, IH), 8.32 (s, IH), 7.74 (m, IH), 7.39 (s, IH), 7.21 (m, 2H), 6.84 (s, IH), 4.32 (t, 2H), 4.28 (m, 2H), 4.01 (s, 3H), 3.95 (s, 2H), 3.56 (br s, 2H), 3.46 (t, 2H), 3.19 (d, 2H), 2.32 (m, 2H), 1.18 (m, IH), 0.68 (m, 2H), 0.47 (m, 2H): MS (+ve ESI): 662.4 (M+H)+.
di-tert-butyl 2- {(cyclopropylmethyl)[3-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l#-pyrazol-3-yl)ammo]-6-memoxyqumazolin-7-yl}oxy)propyl] amino}ethyl phosphate used as starting material was obtained as follows :
a) Ethylchloroformate (4.2 ml, 37 mmol) was added to a stirred solution of cyclopropylmethylamine (3.00 ml, 34.6 mmol) and triethylamine (7 ml) in dichloromethane (35 ml) at 0 °C over 30 minutes. The reaction was stirred at ambient temperature for 2 hours, water (20 ml) was added to the mixture, and the pH adjusted to 3 by addition of 2.0 N hydrochloric acid. The organic phase was separated, dried and concentrated in vacua to yield ethyl (cyclopropylmethyl) carbamate (5.9 g, 100 % yield) :

'H-NMR (CDC13): 7.24 (br s, 1H), 3.24 (m, 2H), 1.43 (t, 3H), 1.04 (m, 1H), 0.59 (m, 2H)3
0.29 (m, 2H):
MS(+veESI):172(M+H)+.
b) A solution of ethyl (cyclopropylrnethyl) carbamate (5.90 g, 34.6 rnniol) in
tetrahydrofuran (30 ml) was added at ambient temperature to a solution of diborane (130 ml
of a 1.0 N solution in tetrahydrofuran, 130 mmol) and chlorotrimethylsilane (34 ml, 268
mmol) and the mixture stirred at ambient temperature for 48 hours. Methanol (20 ml) was
added and the reaction stirred for 30 minutes at ambient temperature. Dichloromethane (25
ml) was added, followed by hydrochloric acid (4 ml of a 6.0 N solution, 24 mmol) and the
reaction was stirred at ambient temperature for 30 minutes. Methanolic ammonia (7.0 N) was
added, the white solid was collected by suction filtration and the organic filtrate was
evaporated in vacua. Purification by chromatography on silica gel, eluting with
dichloromethane to dichloromethane / methanol (95:5) to dichloromethane/ methanol /
ammonia (7.0 N) (90:9:1), yielded 2-((cyclopropylmethyl)arnino)ethanol as a pale yellow
liquid (2.99 g, 75 % yield) :
'H-NMR (DMSO d6, TFA) : 3.66 (t, 2H), 3.02 (t, 2H), 2.84 (d, 2H), 1.06 (m, 1H), 0.58 (m, 2H), 0.35 (m, 2H).
c) An analogous reaction to that described in example 6b, but starting with 2-
(cyclopropyhnethyl)amino)ethanol (115 mg, 1 mmol) yielded2-{3-[(7-{3-
[(cyclopropylmemyl)(2-hydroxyemyl)arriino]propoxy}-6-methoxyquinazolm-4-yl)arnino]-
l//-pyrazol-5-yl}-7V-(2,3-difluorophenyl)acetamide (6 mg, 3 % yield) :
]H-NMR(DMSO d6) : 10.23 (s, 1H), 10.16 (s, 1H), 8.44 (s, 1H), 7.98 (s, 1H), 7.72 (m, 1H),
7.18 (m, 2H), 7.14 (s, 1H), 6.84 (s, 1H), 4.32 (s, 1H), 4.18 (t, 2H), 3.93 (s, 3H), 3.85 (s, 2H),
3.45 (m, 2H), 2.69 (t, 2H), 2.58 (t, 2H), 2.35 (d, 2H), 1.90 (m, 2H), 0.83 (m, 1H), 0.41 (m,
2H), 0.08 (m, 2H) :
MS (+ve ESI): 582.2 (M+H)+.
d) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
[(cyclopropyknethyl)(2-hydroxyethyl)ammo]propoxy}-6-methoxyqumazolin-4-yl)arnino]-
l/f-pyrazol-5-yl}-JV-(2,3-difluorophenyl)acetamide (673 ing, 1.16 mmol) yielded di-tert-butyl
2-{(cyclopropyhiiethyl)[3 yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (HOmg, 12 %
yield):

'H-NMR (DMSO &$ • 10.23 (s, m), 10.15 (s, IH), 8.44 (s, m), 7.98 (s, m), 7.72 (t, IH),
7.19 (IB, 2H), 7.13 (s, IH), 6.83 (s, IH), 4.17 (t, 2H), 3.93 (s, 3H), 3.88 (q, 2H), 3.85 (s, 2H), 2.76 (t, 2H), 2.72 (t, 2H), 2.38 (d, 2H), 1.91 (m, 2H), 1.37 (s, 18H), 0.83 (m, IH), 0.42 (m, 2H), 0.09 (m, 2H) : MS (+ve ESI): 774.7 (M+H)+.
Example 26 - Preparation of compound 26 in table 1 - 2-{cyclobutyir3-({4-r(5-{2-r(3-fluorophenyl)amino1-2-oxoethyl}-lfl-pyrazol-3-vl)amino1-6-methoxyquinazoIin-7-yl>oxy)propyllamino]ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoe1±iyl}-lJJ-pyrazol-3-yl)amino]-6-methoxyqumazolin-7-yl}oxy)propyl]amino} ethyl phosphate (416 ing, 0.55 nimol) yielded compound 26 in table 1 (455 mg, 100 % yield) :
'H-NMR (DMSO d6, TFA) : 8.94 (s, IH), 8.31 (s, IH), 7.65 (d, IH), 7.38 (m, 2H), 7.36 (s, IH), 6.90 (m, IH), 6.83 (s, IH), 4.30 (t, 2H), 4.22 (m, 2H), 4.01 (s, 3H), 3.94 (m, IH), 3.86 (s, 2H), 3.37 (s, 2H), 3.27 (br s, 2H), 2.35 (t, 2H), 2.26 (m, 4H), 1.77 (m, IH), 1.68 (m, IH): MS (+ve ESI) : 644.2 (M+H)+.
di-to-/-butyl2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)aniino]-2-oxoethyl}-lJf-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 5a, but starting with 2- -
(cyclobutylamino)ethanol (178 mg, 1.55 rnmol) yielded 2-{3-[(7-{3-[cyclobutyl(2-
hydroxyethyl)amino]propoxy} -6-methoxyquinazolin-4-yl)amino]- lH-pyrazol-5-yl} -N-(3-
fluorophenyl)acetamide (42 mg, 24 % yield) :
'H-NMR (DMSO d6, TFA): 8.96 (s, IH), 8.29 (s, IH), 7.64 (d, IH), 7.36 (m, 2H), 7.34 (s, IH), 6.90 (t, IH), 6.83 (s, IH), 4.29 (t, 2H), 4.00 (s, 3H), 3.94 (m, IH), 3.85 (s, 2H), 3.75 (m, 2H), 3.25 (m, 2H), 3.17 (m, 2H), 2.08-2.39 (m, 6H), 1.76 (m, IH), 1.69 (m, IH): MS (+ve ESI) : 564.2 (M+H)+.
b) An analogous reaction to that described in example 5b, but starting with 2-{3-[(7-{3-
[cyclobutyl(2-hydroxyethyl)ammo]propoxy}-6-methoxyqumazolm-4-yl)ammo]-lJ/:f-pyrazol-
5-yl}-JV-(3-fluorophenyl)acetamide (474 mg, 0.84 mmol) yielded di-/er/-butyl 2-
{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)aniino]-6-
methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl phosphate (109 mg, 17 % yield) :

'H-NMR (DMSO d6): 10.46 (s, IH), 10.16 (s, IH), 8.44 (s, IH), 7.98 (s, IH), 7.62 (d, IH), 7.34 (m, IH), 7.33 (s, IH), 7.13 (s, IH), 6.89 (t, IH), 6.82 (s, IH), 4.15 (t, 2H), 3.93 (s, 3H), 3.84 (q, 2H), 3.76 (s, 2H), 3.16 (m, IH), 2.64 (t, 2H), 2.59 (t, 2H), 1.96 (m, 2H), 1.88 (m, 2H), 1.77 (m, 2H), 1.55 (m, 2H), 1.38 (s, 18H): MS (+ve ESI): 756.7 (M+H)+.
Example 27 - Preparation of compound 27 in table 2 - 2-{4-[(|4-F(5-{2-r(2,3-difluorophenyDaminol-Z-oxoethyD-lfl-pyrazol-S-vDaminolquinazolin-?-yl)oxy)methyl1piperidin-l-vl|ethvl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{4-[({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoetiyl}-l^-pyrazol-3-yl)amino]quinazolm-7-yl}oxy)methyl]piperidin-l-yl} ethyl phosphate (230 mg, 0.32 mmol) yielded compound 27 in table 2 (230 mg, 95 % yield) as a white solid :
'H-NMR (DMSO d6): 12.00 (s, IH), 10.40 (s, m), 8.95 (s, IH), 8.80 (d, m), 7.70-7.80 (m,
IH), 7.40 (d, IH), 7.35 (s, IH), 7.15-7.25 (m, 2H), 6.70 (s, IH), 4.20-4.30 (m, 2H), 4.05-4.15 (m, 2H), 3.90 (s, 2H), 3.50-3.60 (m, 2H), 3.10-3.25 (m, 2H), 2.27 (m, IH), 2.10-2.20 (m, 2H), 1.70-1.90 (m, 2H), 1.20 (t, 2H) : MS (+ve ESI): 618 (M+H)+, MS(-veESI):616(M-H)'.
di-fert-butyl2-{4-[({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^f-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)methyl]piperidin-l-yl}ethyl phosphate used as starting material was obtained as follows :
a) Dimethylformauaide (0.1 ml) was added to a stirred suspension of 7-(benzyloxy)quinazolin-4(3/f)-one (4.00 g, 15.9 mmol) in thionyl chloride (25 ml) and the reaction heated at 85 °C for 1 hour. The reaction was cooled, the excess thionyl chloride was evaporated in vacua and the residue was azeotroped with toluene (2 x 25 ml) before being taken up in dimethylacetamide (20 ml). 5-amino-lH-pyrazol-3-ylacetic acid (2.27 g, 15.9 mmol) and was added and the reaction was heated at 90 °C for 2.5 hours. The reaction was sooled to ambient temperature, poured into ice-water (200 ml) and the solid which precipitated was collected by suction filtration to yield (3-{[7-(benzyloxy)quinazolin-4-yl]arnino}-l/7-pyrazol-5-yl)acetic acid (3.92 g, 60 % yield) as a pale orange solid:
'H-NMR (DMSO d6) -. 12.70 (br s, m), 8.75 (s, IH), 8.70 (d, m), 7.57 (m, 2H), 7.35-7.50
(m, 4H), 7.30 (s, IH), 6.70 (s, IH), 5.35 (s, 2H), 3.70 (s, 2H):

MS (+ve ESI): 376 (M+H)+, MS(-veESI):374(M-Hy.
b) Phosphorus oxychloride (1.00 ml, 11.6 mmol) was added to a stirred suspension of
2,3-difluoroaniline (1.44 g, 11.6 mmol), (3-{[7-(benzyloxy)qiiinazolin-4-yl]amino}-lH"-
pyrazol-5-yl)acetic acid (3.82 g, 9.30 mmol) and pyridine (40 ml) at 0 °C. The reaction was
stirred for 1 hour at ambient temperature, then cooled to 0 °C and treated with additional
phosphorus oxychloride (0.5 ml) before being allowed to warm to ambient temperature over 1
hour. The reaction was poured into 20% aqueous hydrochloric and the resultant solid was
collected by suction filtration. Prolonged drying in vacuo, yielded 2-(3-{[7-
(benzyloxy)quinazolin-4-yl]amino}-lH-pyrazol-5-yl)-Ar-(2,3-difluorophenyl)acetamide (4.90
g, 100 % yield) as an orange solid which contained some water :
'H-NMR (DMSO d6): 11.30 (s, IH), 10.30 (s, m), s.so (s, m), 8.70 (d, m), 7.80-7.80 (m,
1H), 7.50-7.60 (m, 2H), 7.35-7.45 (m, 5H), 7.30 (s, IH), 7.10-7.20 (m, 2H), 6.80 (s, IH), 5.40(s,2H),3.90(s,2H): MS (+ve ESI) : 487 (M+H)+, MS (-ve ESI): 485 (M-H)".
c) 2-(3- {[7-(benzyloxy)qumazolin-4-yl]arnino}-lfir-pyrazol-5-yl)-A'-(2,3-
difluorophenyl)acetamide (4.90 g, 9.30 mmol) was added to trifluoroacetic acid (75 ml) and
the reaction heated at 90 °C for 4 hours. The reaction was cooled, the excess trifluoroacetic
acid was removed in vacuo and the residue was taken up in methanol (30 ml). The methanolic
solution was added dropwise to aqueous sodium hydrogen carbonate solution (100 ml)
causing precipitation of an orange solid. Collection of the solid followed by washing with
water yielded ^-(2,3-difluorophenyl)-2-{3-[(7-hydroxyquinazolm-4-yl)arnino]-lj?;r-pyrazol-5-
yljacetamide (3.60 g, 97 % yield) as a pale brown solid after drying in vacuo :
'H-NMR (DMSO d6): 12.50 (br s, m), 10.30 (s, IH), 8.70 (s, IH), 8.60 (d, IH), 7.70-7.80
(m, IH), 7.30-7.40 (m, 2H), 7.10 (d, IH), 7.00 (s, IH), 6.80 (br s, IH), 3.80 (s, 2H): MS (+ve ESI) : 397 (M+H)+, MS (-ve ESI) : 395 (M-H)".
d) Methanesulphonyl chloride (864 mg, 7.58 mmol) was added dropwise to a solution of
Ar-(/er/-butoxycarbonyl)piperidin-4-yhiiethanol (1.63 g, 7.58 mmol) and triethylamine (1.40
ml, 10.0 mmol) in dry tetrahydrofuran (15 ml) at 0 °C and the reaction was stirred at this
temperature for 1 hour. The reaction was filtered, the residue was washed with diethyl ether
and the combined organic phases were evaporated in vacuo to afford a colourless oil. The oil

was taken up in dimethylacetamide (10 ml), Ar-(2,3-difluorophenyl)-2-{3-[(7-hydroxyquinazolin-4-yl)amino]-lff-pyrazol-5-yl}acetamide (2.00 g, 5.07 mmol) and potassium carbonate (1.39 g, 10.0 mmol) were added and the reaction heated at 70 °C for 16 hours. The reaction mixture was concentrated in vacua and purified by flash chromatography on silica gel, eluting with 0-5% methanol in dichloromethane, to yield /e/'f-butyl 4-[({4-[(5-{2-[(2,3-difluorophenyl)arnino]-2-oxoethyl}-lff-pyrazol-3-yl)arnino]quinazoUn-7-yl}oxy)methyl]piperidin-l-ylcarboxylate (1.11 g, 38% yield) as a yellow solid : ]H-NMR (DMSO dc) : 12.50 (s, 1H), 10.30 (d, 2H), 8.60-8.70 (m, 2H), 7.70-7.80 (m, 1H), 7.30-7.40 (rn, 4H), 6.90 (s, 1H), 4.00-4.10 (m, 4H), 3.90 (s, 2H), 2.80-2.90 (m, 2H), 2.00-2.10 (m, 1H), 1.80-1.90 (m, 2H), 1.50 (s, 9H), 1.30-1.40 (m, 2H): MS (+ve ESI) : 594 (M+H)+, MS (-ve ESI): 592 (M-H)~.
e) Trifluoroacetic acid (5 ml) was added to a solution of te/-/-butyl 4-[({4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)methyl]piperidin-l-ylcarboxylate (1.11 g, 1.897 mmol) in dichloromethane (25 ml) and the reaction stirred for 30 minutes at ambient temperature. The volatile substances were removed in vacuo and the product was purified by reverse phase hplc. The fractions from the hplc were concentrated in vacuo to 20% of their original volume and made basic with sodium carbonate, causing precipitation of an orange solid. The solid was collected by suction filtration., dissolved in dichloromethane : methanol (1:9) and washed with water. Solvent evaporation in vacuo yielded JV-(2,3-difluorophenyl)-2-(3-{[7-(piperidin-4-yknethoxy)quinazolin-4-yl]amino}-lf/-pyrazol-5-yl)acetamide (612 mg, 66 % yield) as an orange powdery solid :
2H-NMR (DMSO d6): 12.40 (s, 1H), 10.20 (br s, 2H), 8.50-8.60 (m, 2H), 7.70-7.80 (m, 1H), 7.00-7.20 (m, 4H), 6.70 (br s, 1H), 4.20 (br s, 1H), 4.00 (d, 2H), 3.90 (s, 2H), 3.10-3.20 (rn, 2H), 2.90-3.00 (m, 2H), 1.90-2.00 (m, 1H), 1.70-1.80 (m, 2H), 1.20-1.30 (m, 2H): MS (+ve ESI): 494 (M+H)+, MS (-ve ESI): 492 (M-H)'.
f) Sodium acetoxyborohydride (392 mg, 1.86 mmol) was added to a solution oftert-butyldimethylsilyloxyacetaldehyde (324 mg, 1.86 mmol), Ar-(2,3-difluorophenyl)-2-(3-{[7-(piperidin-4-ylmethoxy)qumazolm-4-yl]amino}-lH-pyrazol-5-yl)acetamide (612 mg, 1.24 mmol), acetic acid (0.42 ml, 7.4 mmol) in methanol (10 ml) and tetrahydrofuran (30 ml) and the reaction stirred for 18 hours at ambient temperature. Additional sodium

acetoxyborohydride (392 mg, 1.86 mmol) and ter/-butyldimethylsilyloxyacetaldehyde (324
mg, 1.86 rnmol) were added and the reaction stirred for 10 minutes before being concentrated
in vacua. The residue was purified by flash chromatography on a Biotage 40M cartridge,
eluting with methanol: dichloromethane (7:93) and then 7.0N ammonia methanol (1:99) to
give 2- {3 -[(7- {[ 1 -(2- {[tert-butyl(drmethyl)silyl]oxy} ethyl)piperidin-4-
yljmethoxy} qumazoUn-4-yl)aminoj- l£f-pyrazol-5-yl} -JV-(2,3-difluorophenyl)acetamide (410
mg, 51 % yield) as a pale orange solid after solvent evaporation and drying in vacua :
'H-NMR (DMSO d6): 12.40 (s, IH), 10.15 (s, IH), 10.10 (s, IH), 8.50 (s, IH), 8.45 (d, IH),
7.60-7.70 (m, IH), 7.00-7.20 (in, 4H), 6.70 (s, IH), 3.90 (d, 2H), 3.70 (s, 2H), 3.60 (t, 2H),
2.80-2.90 (m, 2H), 2.40 (t, 2H), 1.90-2.00 (m, 2H), 1.70-1.80 (m, 3H), 1.20-1.30 (m, 2H),
0.80 (s, 9H), 0.00 (s, 6H) :
MS (+ve ESI): 652 (M+H)+,
MS (-ve ESI) : 650 (M-H)'.
g) re/ra-«-butylammoniuin fluoride (0.69 ml of a 1 .ON solution in tetrahydrofuran, 0.69
mmol) was added to a solution of 2- {3-[(7- {[1 -(2-{[tert-
butyl(dimethyl)silyl]oxy} ethyl)piperidin-4-yl]methoxy} quinazolin-4-yl)amino]- l#-pyrazol-
5-yl}-JV-(2,3-difluorophenyl)acetamide (410 nig, 0.63 mmol) in tetrahydrofuran (10 ml). The
reaction was stirred for 18 hours at ambient temperature, during which time 2 additional
portions of te/ra-«-butylammonium fluoride (0.69 mmol) were added. The reaction was
concentrated in vacua and the residue was purified by flash chromatography on a Biotage 40S
cartridge, eluting with methanol: dichloromethane (25:75) and then 7.0N ammonia :methanol
(1:99) to give A^-(2,3-difluorophenyl)-2-{3-[(7-{[l-(2-hydi-oxyethyl)piperidin-4-
yl]methoxy}qumazolin-4-yl)amino]-lH-pyrazol-5-yl}acetarnide (258 mg, 76 % yield) as a
pale orange solid:
'H-NMR (DMSO dfi): 12.30 (s, IH), 10.30 (br s, IH), 8.50 (br s, 2H), 7.76 (m, IH), 7.10-
7.40 (m, 4H), 6.90 (br s, IH), 4.40 (br s, IH), 4.10 (d, 2H), 3.80 (br s, 2H), 3.40-3.50 (m, 2H),
2.90-3.00 (m, 2H), 2.50 (t, 2H), 2.00-2.10 (m, 2H), 1.70-1.80 (m, 3H), 1.30-1.40 (m, 2H) :
MS (+ve ESI) : 538 (M+H)+,
MS (-ve ESI) : 536 (M-H)".
h) An analogous reaction to that described in example 6c, but starting with N-(2,3-
difluorophenyl)-2- {3-[(7- {[ 1 -(2-hydroxyethyl)piperidin-4-yl]methoxy} quinazolin-4-
yl)ammo]-l#-pyrazol-5-yl}acetamide (235 mg, 0.44 mmol) yielded di-ter/-butyl 2-{4-[({4-

[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]quiiiazolin-7-yl}oxy)methyl]piperidin-l-yl}ethyl phosphate (232 mg, 73 % yield) as a white solid : 'H-NMR (DMSO dfi) •: 12.30 (s, IH), 10.20 (d, 2H), 8.40 (br s, 2H), 7.60-7.70 (m, IH), 7.30-7.40 (m, 4H), 6.80 (br s, IH), 4.05 (d, 2H), 3.92 (m, 2H), 3.80 (br s, 2H), 2.80-2.90 (m, 2H), 2.50 (t, 2H), 2.00-2.10 (m, 2H), 1.60-1.70 (m, 3H), 1.40 (s, 18H), 1.20-1.30 (m, 2H): MS (+ve ESI) : 730 (M+H)+, MS (-ve ESI) : 728 (M-H)'.
Example 28 - Preparation of Compound 28 in table 3 - 2-rf3-((4-r(5-|2-rC2,3-difluorophenyl)amino1-2-oxoethvl}-lfl-pvrazol-3-vl)amino1-quinazoIin-7-yl}oxy)propyI1(ethyl)aniinolethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(te;-*-butyl) 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)airuno]-2-oxoemyl}-lF-pyrazol-3-yl)ainino]-quinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl phosphate (302 mg, 0.422 mmol) yielded compound 28 in table 3 (300 mg, 100 % yield) as a white solid :
'H-NMR (DMSO d6): 12.00 (s, m), 10.30 (s, m), 8.90 (d, m), 7.65-7.75 (m, m), 7.50-
7.60 (m, 2H), 7.10-7.25 (m, 2H), 6.70 (s, IH), 4.35 (t, 2H), 4.20-4.30 (m, 2H), 3.90 (s, 2H), 3.40-3.50 (m, 2H), 3.25-3.3.5 (m, 2H), 3.10-3.20 (m, 2H), 2.20-2.40 (M, 2H), 1.30 (t, 3H) : MS (+ve ESI) : 606 (M+H)+, MS (-ve ESI): 604 (M-H)".
di(/ert-butyl)2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](ethyl)amino] ethyl phosphate used as starting material was obtained as follows: a) 2-Amino-4-fluorobenzoic acid (15 g, 96 mmol) was dissolved in 2-methoxyethanol
b) Sodium hydride (14.6 g, 365 mmol) was added at 0 °C to a solution of 1,3-propanediol
(27.8 g, 365 mmol) in dimethylformamide (70 ml). 7-Fluoroquinazolin-4(3H)-one (10 g, 60.9
mmol) was added portionwise and the reaction mixture heated at 60 °C, then at 110 °C for 3
hours. The reaction was cooled to 0 °C, quenched with water (280 ml) and adjusted to pH 5.9.
The resulting suspension was filtered, washed with water then ether and dried over
phosphorus pentoxide to afford 7-(3-hydroxypropoxy)quinazolin-4(3H)-one as a white
powder (12.41 g, 92 % yield) :
'H-NMR (DMSO d6): 11.90 (br s, 1H), 8:04 (s, 1H), 8.00 (d, 1H), 7.10 (m, 2H), 4.17 (t, 2H), 3.58 (t,2H), 1.92 (m, 2H) : MS (+ve ESI) : 221 (M+H)+.
c) 7-(3-hydroxypropoxy)quinazolin-4(3H)-one (10.5 g, 47.7 mmol) and thionyl chloride
(100 ml, 137 mmol) were combined. Dimethylformamide (1 ml) was added and the reaction
mixture heated to 85 °C for 1 hour. The mixture was cooled to room temperature, diluted with
toluene and evaporated to dryness. This was repeated until all thionyl chloride was removed.
The residue was dissolved in dichloromethane and washed with a saturated sodium
bicarbonate solution. The aqueous layer was extracted with dichloromethane. The organics
were combined, dried (magnesium sulphate) and concentrated to leave a yellow solid.
Trituration with ether removed a less soluble impurity and the ether filtrate was concentrated
to leave 4-chloro-7-(3-chloropropoxy)quinazoline as an off-white solid (8.5 g, 70 % yield) :
'H-NMR (DMSO d6).-13.25 (br s, m), 8.34 (s, m), s.oe (d, m), 7.17 (m, 2H), 4.21 (t, 2H),
3.83 (t, 2H), 2.23 (m, 2H) :
MS (+ve ESI) : 257, 259 (M+H)+.
d) 4-chloro-7-(3-chloropropoxy)quinazoline (2.5 g, 9.72 mmol) and (3-acn.in.o-IH-
pyrazol-5-yl)acetic acid (1.37 g, 9.72 mmol) were combined in dimethylformamide (25 ml).
A solution of 4M HC1 in dioxane (1.25 ml, 4.8 mmol) was added and the reaction heated to
90 °C for 40 minutes. The solution was cooled to room temperature, diluted with water (250
ml) and filtered through celite. The acidic solution was basified to pH 4.9 and the yellow
powder filtered. (At pH 3, a red solid precipitated which was isolated, suspended in water and
basified to pH 12. Careful adjustment back to pH 4.8 resulted in the precipitation of a yellow
powder, which was combined with the first crop). The solid was washed with diethyl ether
and dried over phosphorus pentoxide to yield (3-{[7-(3-chloropropoxy)quinazolin-4-
yl]amino}-l#-pvrazol-5-yr)acetic acid as a pale orange solid (2.88 g, 82 % yield):
'H-NMR (DMSO dfi): 12.60 (br s, 2H), 10.78 (br s, 1H), 8.65 (s, 1H), 8.60 (d, 1H), 7.26 (d, 1H), 7.22 (s, 1H), 6.67 (s, 1H), 4.28 (t, 2H), 3.83 (t, 2H), 3.67 (s, 2H), 2.24 (m, 2H) : MS (-ve ESI) : 360, 362 (M-H)', MS (+ve ESI): 362, 364 (M+H)+.
e) 2,3-difluoroaniline (1.15 g, 8.95 mmol) was added to a suspension of (3-{[7-(3-chloropropoxy)quinazolin-4-yl]amino}-lfl'-pyrazol-5-yl)acetic acid (2.70 g, 7.46 mmol) in pyridine (30 ml) and the reaction cooled to 0 °C. Phosphorous oxychloride (1.14 g, 7.46 mmol) was added dropwise and the reaction stirred at 0 °C for 1 hour. The reaction was warmed to ambient temperature and more phosphorous oxychloride (0.5 ml) added. The reaction was stirred for 4.5 hours. The reaction mixture was diluted with ethyl acetate : ether (100 ml: 37 ml) and stirred for 18 hours. The precipitate was filtered, suspended in water and neutralised with ammonium hydroxide (7 %, 15 ml). The resultant yellow suspension was filtered, washed with water and dried (phosphorous pentoxide) to yield 2-(3-{[7-(3-chloropropoxy)qimia2olm-4-yl]arm^o}-l/f-pyrazol-5-yl)-A'-(2,3-difluorophenyl)acetarnideas an orange powder (3.15 g, 89 % yield):
'H-NMR (DMSO d6): 10.64 (br s, 1H), 10.27 (s, 1H), 8.60 (s, 1H), 8.55 (d, 1H)3 7.70 (m, 1H), 7.20 (m, 6H), 6.68 (s, 1H), 4.27 (t, 2H), 3.83 (m, 4H), 2.25 (m, 2H): MS (-ve ESI): 471,473 (M-H)', MS (+ve ESI) : 473, 475 (M+H)+.
f) 2-(3- {[7-(3-chloropropoxy)quinazolin-4-yl]amino} -lH-pyrazol-5-yl)-N-(2,3-difluorophenyl)acetamide (300 mg, 0.634 mmol), potassium iodide (210 rag, 1.27 mmol), dimethylamine (2 ml) and 2-(ethylamino)ethanol (226 mg, 2.54 mmol) were combined and heated to 50 °C for 72 hours. The reaction was diluted with dichloromethane (20 ml) and loaded onto a 40S silica biotage column. Elution with dichloromethane followed by increased polarity to dichloromethane : methanol (9:1), then dichloromethane: methanol: ammonia (9:1:0.8) yielded 7V-(2,3-difluorophenyl)-2-{3-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}-quinazolin-4-yl)ammo]-ljcf-pyrazol-5-yl}acetamide as a pale pink solid (181 mg, 54 % yield): 'H-NMR (DMSO d6) : 12.35 (s, 1H), 10.25 (s, 2H), 8.52 (s, 2H), 7.71 (m, 1H), 7.16 (m, 4H), 6.78 (s, 1H), 4.33 (t, 1H), 4.17 (t, 2H), 3.84 (s, 2H), 3.43 (m, 2H), 2.60 (t, 2H), 2.49 (m, 4H), 1.88(m,2H),0.96(t, 3H): MS (-ve ESI): 524 (M-H); MS (+ve ESI) : 526 (M+H)+.
g) An analogous reaction to that described in example 6c, but starting with N-(2,3-difluoroplienyl)-2- {3-[(7- {3-[ethyl(2-hydroxyethyl)amino]propoxy} -quinazolin-4-yl)amino] -l#-pyrazol-5-yl}acetamide (372 mg, 0.71 mmol) yielded di(tert-butyl) 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lJy-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](ethyl)amino]ethyl phosphate (304 mg, 60 % yield) as a pale yellow solid: 'H-NMR pMSO d6): 12.30 (s, IH), 10.20 (d, 2H), 8.60-8.70 (m, 2H), 7.70-7.80 (m, IH), 7.05-7.25 (m, 4H), 6.80 (br s, IH), 4.20 (t, 2H), 3.80-3.90 (m, 4H), 2.60-2.70 (m, 4H), 2.40-2.50 (m, 2H), 1.80-1.90 (m, 2H), 1.40 (s, 18H), 0.95 (t, 3H) : MS(+veESI):718(M+H)+, MS(-veESI):716(M-H)".
Example 29 - Preparation of compound 29 in table 3 - 2-ff3-f|4-rrS-l2-r(2,3-difluorophenyl)amino]-2-oxoethvl}-lfl-pyrazol-3-yl)amino1-quina2oIin-7-vl}oxv)propyll(isopropyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/y-pyrazol-3-yl)arnino]-quinazolin-7-yl}oxy)propyl](isopropyl)amino]ethyl phosphate (372 mg, 0.51 mmol) yielded compound 29 in table 3 (342 mg, 92 % yield) as a pale yellow solid :
]H-NMR (DMSO d6) : 12.00 (s, IH), 10.30 (s, IH), 8.90 (s, IH), 8.80 (d, IH), 7.60-7.70 (m, IH), 7.40-7.50 (m, 2H), 7.10-7.20 (m, 2H), 6.70 (s, IH), 4.40 (t, 2H), 4.20-4.30 (m, 2H), 3.90 (s, 2H), 3.70-3.80 (m, IH), 3.40-3.50 (m, 2H), 3.20-3.30 (m, 2H), 2.30-2.40 (m, 2H), 1.35 (d, 6H):
MS (+ve ESI): 620 (M+H)+, MS(-veBSI):618(M-H)".
di-fe7'/-butyl2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)arnino]-2-oxoethyl}-lJff-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](isopropyl)amino]ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with 2-(isopropylamino)ethanol (262 mg, 2.54 mmol) yielded JV-(2,3-difluorophenyl)-2-{3-[(7- {3-[isopropyl(2-hydroxyethyl)amino]propoxy}-quinazolin-4-yl)amino]-lJH-pyrazol-5-yl}acetamide as an off-white solid (182 mg, 53 % yield) :
'H-NMR (DMSO dfi) : 12.35 (s, IH), 10.20 (s, IH), 8.50 (s, 2H), 7.71 (m, IH), 7.20 (m, 4H), 6.78 (s, IH), 4.29 (br s, IH), 4.19 (t, 2H), 3.85 (s, 2H), 3.38 (dt, 2H), 2.88 (m, IH), 2.55 (t, 2H), 2.45 (t, 2H), 1.82 (m, 2H), 0.93 (d, 6H): MS (-ve ESI): 538 (M-H)', MS (+ve ESI): 540 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with N-(2,3-difluorophenyl)-2- {3-[(7- {3-[isopropyl(2-hydroxyethyl)amino]propoxy} -quinazolin-4-yl)amino]-lF-pyrazol-5-yl}acetamide (414 mg, 0.77 mmol) yielded di-tert-butyl 2-[[3-({4-[(5 - {2 - [(2,3 -difluorophenyl)amino] -2-oxoethyl} -1 7f-pyrazol~3-yl)amino] -quinazolin-7-yl}oxy)propyl](isopropyl)amino]ethyl phosphate (374 nag, 67 % yield) as a white solid : 'H-NMR (DMSO d6) : 12.40 (s, IH), 10.20 (d, 2H), 8.50-8.60 (m, 2H), 7.60-7.80 (m, IH), 7.10-7.30 (m, 4H), 6.80 (br s, IH), 4.15-4.25 (m, 2H), 3.80-3.90 (m, 4H), 2.85-3.00 (m, IH), 2.50-2.65 (m, 4H), 1.80-1.90 (m, 2H), 1.40 (s, 18H), 1.00 (s, 3H), 0.98 (s, 3H) : MS (+ve ESI) : 732 (M+H)+, MS (-ve ESI) : 730 (M-H)'.
Example 30 - Preparation of compound 30 in table 3 - 3-ir3-f(4-r(5-l2-f(2.3-difluorophenyI)amino1-2-oxoethyI}-lg-pyrazol-3-yI)amino1quinazoIin-7-yl}oxy)propyllamino}-3-methyIbutyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-ter/-butyl 3-{[3-({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoethyl}-l.ZJ-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino}-3-methylbutyl phosphate (490 mg, 0.67 mmol) yielded compound 30 in table 3 (480 mg, 99 % yield) as a pale yellow dihydrochloride salt:
'H-NMR (DMSO d6): 12.00 (s, IH), 10.35 (s, m), 9.20 (br s, m), 8.90 (s, m), s.so (d, m),
7.72 (m, IH), 7.50 (d, 2H), 7.40 (s, IH), 7.20-7.30 (m, 2H), 6.70 (s, IH), 4.30 (t, 2H), 3.90-
4.00 (m, 2H), 3.85 (s, 2H), 3.10-3.20 (m, 2H), 2.20-2.30 (m, 2H), 2.00-2.10 (m, 2H), 1.40 (d,
6H) :
MS (+ve ESI): 620 (M+H)+.
MS(-veESI):618(M-HT.
di-fe^buryl3-{[3-({4-[(5-{2-[(2,3-difluorophenyl)arnino]-2-oxoethyl}-l//-pyrazol-3-
yl)amino]quinazolin-7-yl}oxy)propyl]amino}-3-methylbutyl phosphate used as starting
material was obtained as follows :

a) An analogous reaction to that described in example 28f, but starting with 3-amino-3-
methylbutan-1-ol (655 mg, 6.36mmol) yielded N-(2,3-difluorophenyl)-2-{3-[(7-{3-[(3-
hydroxy-1,1 -dimethylpropyl)amino]propoxy} quinazolin-4-yl)amino] -1 #-pyrazol-5-
yl}acetamide as an off-white solid (450 mg, 39 % yield) :
'H-NMR (DMSO d6): 12.40 (s, IH), 10.20 (br s, 2H), 8.60-8.70 (m, 2H), 7.70-7.80 (m, IH), 7.25-7.35 (m, 4H), 6.80 (br s, IH), 4.20 (t, 2H), 3.90 (s, 2.H), 3.60 (t, 2H), 2.70 (t, 2H), 1.90-2.00 (m, 2H), 1.50 (t, 2H), 1.00 (s, 6H) : MS (+ve ESI) : 540 (M+H)+, MS (-ve ESI): 538 (M-H)'.
b) An analogous reaction to that described in example 6c, but starting with JV-(2,3-
difluorophenyl)-2- {3-[(7-{3-[(3 -hydroxy-1,1 -dimethylpropyl)amino]propoxy} quinazolin-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (212 mg, 0.38 mmol) yielded di-/ert-butyl 3-{[3-({4-
[(5-{2-[(23-difluorophenyl)amino]-2-oxoe1±iyl}-lH-pyrazol-3-yl)amino]quinazolin-7-
yl}oxy)propyl]amino}-3-methylbutyl phosphate (204 mg, 72 % yield) as a pale yellow solid:
'H-NMR (DMSO d6) : 12.40 (s, IH), 10.20 (d, 2H), 8.50-8.60 (m, 2H), 7.65-7.75 (m, IH),
7.20-7.30 (m, 4H), 6.80 (s, IH), 4.30 (t, 2H), 3.90-4.00 (m, 2H), 3.85 (s, 2H), 2.70-2.80 (m,
2H), 1.90-2.00 (m, 2H), 1.60-1.70 (m, 2H), 1.40 (s, 18H), 1.10 (s, 6H) :
MS (+ve ESI): 732 (M+H)+, MS (-ve ESI) : 730 (M-HT.
Example 31 - Preparation of Compound 31 in table 3 - 2-U2S)-I-\3-((4-f(5-{2-f(2,3-difluorophenyl)amino1-2-oxoethyl|-lg-pyrazoI-3-yl)amino1-quinazoIin-7-yI}oxy)propyl1pyrrolidin-2-yl)ethyI dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(?e/Y-butyl) 2-{(2,S)-l-[3-({4-[(5-{2-[(2,3-difluorophenyl)airuno]-2-oxoethyl}-lff-pyrazol-3-yl)aniino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl} ethyl phosphate (204mg, 0.27 mmol) yielded compound 31 in table 3 (198 mg, 97 % yield) as a pale yellow dihydrochloride salt: 'H-NMR (DMSO d6): 12.00 (s, IH), 10.80 (s, IH), 10.50 (s, IH), 8.95 (s, IH), 8.80 (d, IH), 7.60-7.80 (m, IH), 7.50 (d, IH), 7.40 (s, IH), 7.20-7.30 (m, 2H), 6.70 (s, IH), 4.35 (t, 2H), 3.90-4.00 (m, IH), 3.85 (s, 2H), 3.60-3.70 (m, IH), 3.30-3.50 (m, 2H), 3.00-3.25 (m, 2H), 2.20-2.40 (m, 4H), 1.90-2.10 (m, 3H), 1.70-1.80 (m, IH) : MS (+ve ESI): 632 (M+H)*, MS (-ve ESI): 630 (M-H)'.

di(ter/-butyl)2-{(26)-l-[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with (2S)-2-(2-
hydroxyethyl)pyrrolidine (731 mg, 6.36 mmol) yielded ^-(2,3-difluorophenyl)-2-{3-[(7-{3-
[(2lS)-2-(2-hydroxyethyl)pyrrolidin-l-yl]propoxy}-quinazolin-4-yl)amino]-l/:f"-pyrazol-5-
yljacetamide as a white solid (260 mg, 22 % yield) :
'H-NMR (DMSO d6) : 12.30 (s, IH), 10.20 (s, 2H), 8.40-8.70 (m, 2H), 7.70-7.80 (m, IH), 7.10-7.30 (m, 4H), 6.80 (br s, IH), 4.30-4.50 (m, IH), 4.20 (t, 2H), 3.80-3.90 (m, 2H), 3.30-3.50 (m, 2H), 3.10-3.20 (m, IH), 2.90-3.00 (m. IH), 2.30-2.40 (m, IH), 2.10-2.20 (m, IH), 1.90-2.00 (m, IH), 1.75-1.85 (m, 3H), 1.68 (m, IH), 1.50-1.60 (m, 2H), 1.30-1.40 (m, 2H) : MS (+ve ESI): 520 (M+H)+, MS (-ve ESI) : 550 (M-H)'.
b) An analogous reaction to that described in example 6c, but starting with 7V-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(2iS}-2-(2-hydVoxyemyl)pyrroh'dm-l-yl]propoxy}-quinazolin-4-
yl)amino]-lH-pyrazol-5-yl}acetamide (212 mg, 0.38 mmol) yielded di(te7-/-butyl) 2-{(25)-l-
[3-({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoemyl}-l//-pyrazol-3-yl)arnino]-quinazolin-
7-yl}oxy)propyl]pyrrolidin-2-yl} ethyl phosphate (204 mg, 72 % yield) as a pale yellow solid:
'H-NMR (DMSO d6, 373K) : 12.00 (s, IH), 9.90 (s, 2H), 9.80 (s, IH), 8.50 (s, IH), 8.40 (d,
IH), 7.70-7.80 (m, IH), 7.20-7.30 (m, 4H), 6.70 (br s, IH), 4.30 (t, 2H), 3.90-4.00 (m, 2H),
3.80 (s, 2H), 3.00-3.10 (m, IH), 2.40-2.50 (m, IH), 2.20-2.30 (m, IH), 1.80-2.00 (m, 4H),
1.70-1.80 (m, 2H), 1.62 (m, IH), 1.40-1.50 (m, IH), 1.40 (s, 18H), 0.90-1.00 (m, IH):
MS (+ve ESI): 742 (M+H)+, MS (-ve ESI) : 740 (M-H)~.
Example 32 - Preparation of Compound 32 in table 3 - {(2^)-l-r3-f|4-r(5-{2-r(2,3-difluorophenvDaminol-Z-oxoethylj-lg-pyrazol-S-yDaminol-quinazolin-?-yl}oxy)propyl1pyrroIidin-2-yl} methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(/e/^-buryl) {(2/?)-l-[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lJH'-pyrazol-3-yl)amino]-}uinazolm-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (355 mg, 0.49 rnmol) yielded compound 32 in table 3 (355 mg, 100 % yield) as a pale yellow dihydrochloride salt (as the dihydrate) :

!H-NMR (DMSO d6) : 12.00 (br s, IH), 10.40 (s, IH), 8.93 (s, IH), 8.82 (d, IH), 7.68 (m, IH), 7.40-7.50 (m, 2H), 7.15-7.25 (m, 2H), 6.75 (s, IH), 4.35 (t, 2H), 4.10-4.30 (m, IH), 3.92 (s, 2H), 3.81 (m, IH), 3.55-3.70 (m, 2H), 3.27 (m, IH), 3.18 (m, IH), 2.10-2.35 (m, 4H), 1.85-2.10 (m, 3H), 1.75-1.85 (m, IH): MS(+veESI):618(M+H)+.
di(tert-butyl) {(2R)-1 -[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl} -lF-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with D-prolinol
(257 mg, 2.54 rnrnol) yielded A^-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2^)-2-
(hydroxymethyl)pyrrolidm-l-yl]propoxy}-quinazolin-4-yl)amino]-l//-pyrazol-5-
yl}acetamide as a pink solid (206 mg, 60 % yield) :
'H-NMR (DMSO d6): 11.60 (br s, 7H), 10.25 (s, IH), 8.52 (m, 2H), 7.75 (m, IH), 7.16 (m, 4H), 6.67 (s, IH), 4.22 (t, 2H), 3.84 (s, 2H), 3.50 (d, 2H), 3.35 (rn, IH), 3.28 (m, IH), 3.07 (m, IH), 2.86 (m, IH), 2.72 (m, IH), 2.05 (m, 2H), 1.95 (in, IH), 1.60-1.90 (m, 4H) : MS (-ve ESI) : 536 (M-H)', MS (+ve ESI) : 538 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with ^-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(2^)-2-(hydroxyrnethyl)pyrrolidin-l-yl]propoxy}-quinazolin-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (437 mg, 0.81 mmol) yielded di(tert-butyl) {(2J?)-l-[3-
({4-[(5-{2-[(2,3-difluorophenyl)mnmo]-2-oxoemyl}-l/:/-pyrazol-3-yl)arriino]-qumazolin-7-
yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (355 mg, 60 % yield) as a pale yellow solid :
'H-NMR (DMSO d6): 12.30 (br s, m), 10.20 (s, 2H), 8.50 (s, 2H), 7.68 (m, m), 7.10-7.20
(m, 4H), 6.78 (br s, IH), 4.15 (t, 2H), 3.80 (m, 3H), 3.65 (m, IH), 3.10 (m, 1H)3 2.93 (m, IH), 2.64 (m, IH), 2.19 (m, IH), 1.80-1.95 (m, 3H), 1.68 (m, 2H), 1.60 (m, IH), 1.33 (s, 18H) : MS(-veESI):728(M-H)~, MS (+ve ESI): 730 (M+H)+.
Example 33 - Preparation of compound 33 in table 3 - 2-fr3-((4-KS-|2-fr2,3-difluorophenvl)amino]-2-oxoethyI)-lfl-pyrazoI-3-yl)amino1-quinazoIin-7-yl}oxy)propyl1 (prop vDaminol ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} - l/7-pyrazol-3-yl)arnino]-quinazolin-

7-yl}oxy)propyl](propyl)amnio]ethyl phosphate (271 mg, 0.37 mmol) yielded compound 33 in table 3 (266 mg, 98 % yield) as the dihydrochloride salt:
'H-NMR (DMSO d6>): 12.02 o>r s, m), 10.40 (s, IH), 9.95 (s, IH), 9.85 (s, IH), 7.70 (s, IH),
7.47 (m, 2H), 7.20 (m, 2H), 6.73 (s, IH), 4.23-4.37 (m, 4H), 3.92 (s, 2H), 3.43 (m, 2H), 3.32
(m, 2H), 3.13 (m, 2H), 2.28 (m, 2H), 1.76 (m, 2H), 0.95 (t, 3H) :
MS (+ve ESI): 618.4 (M+H)+,
MS (-ve ESI): 620.4 (M-H)'.
di-/er/-butyl 2-[[3 -({4-[(5- {2-[(2,3-difluorophenyl)amino] -2-oxoethyl} - ltf-pyrazol-3 -
yl)amino]-quinazolm-7-yl}oxy)propyl](propyl)amino]ethyl phosphate used as starting
material was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with 2-
(propylamino)ethanol (262 mg, 2.54 mmol) yielded JV-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyethyl)(propyl)amino]propoxy}-quinazolin-4-yl)amino]-l//'-pyrazol-5-yl}acetamide as
a pink solid (168 mg, 49 % yield):
'H-NMR (DMSO d6): 12.35 (s, IH), 10.22 (s, 2H)5 s.si (s, 2H), 7.71 (m, IH), 7.20 (m, 4H),
6.78 (s, IH), 4.30 (t, IH), 4.17 (t, 2H), 3.85 (s, 2H), 3.43 (m, 2H), 2.59 (t, 2H), 2.49 (m, 2H), 2.39 (t, 2H), 1.87 (m, 2H), 1.39 (m, 2H), 0.82 (t, 3H) : MS (-ve ESI): 538 (M-H)', MS (+ve ESI): 540 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 7V-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(propyl)amino]propoxy}-quinazolin-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (690 mg, 1.28 mmol) yielded di-tert-butyl 2-[[3-({4-
[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoemyl}-lJY-pyra2;ol-3-yl)amino]-quinazolin-7-
yl}oxy)propyl](propyl)amino]ethyl phosphate (271 mg, 29 % yield) as a pale yellow solid :
MS (-ve ESI) : 730 (M-H)",
MS (+ve ESI) : 732 (M+H)+.
Example 34 - Preparation of compound 34 in table 3 - 2-rr3-((4-[(5-(2-f(2,3-difluorophenvI)aminol-2-oxoethyl|-lJy-pyrazol-3-yl)amino1-quinazolin-7-yl}oxy)propyl1fbutyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(te/'f-butyl) 2-[[3
quinazolm-7-yl}oxy)propyl](hutyl)amino]ethyl phosphate (400 mg, 0.54 rnmol) yielded compound 34 in table 3 (360 mg, 95 % yield) as a pale yellow dihydrochloride salt:
'H-NMR PMSO d6): 12.00 (s, m), 10.34 (s, m), 8.93 (s, IH), 8.85 (d, m), 7.68 (m,
7.47 (d, IH), 7.44 (s, IH), 7.20 (m, 2H), 6.74 (s, IH), 4.33 (t, 2H), 4.28 (m, 2H), 3.93 (s, 2H),
3.44 (m, 2H), 3.36 (m, 2H), 3.16 (m, 2H), 2.30 (m, 2H), 1.71 (m, 2H), 1.34 (m, 2H), 0.93 (t,
3H):
MS (+ve ESI): 634 (M+H)+.
di(tert-butyl) 2-[[3-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-
yl)amino]-quinazolin-7-yl}oxy)propyl](butyl)amino]ethyl phosphate used as starting material
was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with 2-
(butylamino)ethanol (891 mg, 7.61 mmol) yielded Ar-(2,3-difluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyethyl)(butyl)amino]propoxy}-qumazolia-4-yl)amino]-l/f-pyrazol-5-yl}acetamideas
a pale yellow solid (625 mg, 45 % yield):
'H-NMR (DMSO d6): 12.65(s, IH), 12.32 (s, IH), 10.17 (m, 2H), 8.52 (m, 2H), 7.72 (m, IH), 7.05-7.30 (m, 4H), 6.78 (br s, IH), 4.30 (m, IH), 4.20 (t, 2H), 3.85 (br s, 2H), 3.44 (m, 2H), 2.63 (m, 2H), 2.54 (m, 2H), 2.45 (m, 2H), 1.90 (m, 2H), 1.38 (m, 2H), 1.26 (m, 2H), 0.84 (t, 3H) : MS (+ve ESI): 554 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with N-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(butyl)amino]propoxy}-quinazolin-4-
yl)amino]-lfl"-pyrazol-5-yl}acetamide (605 mg, 1.09 mmol) yielded di(ter/-butyl) 2-[[3-({4-
[(5-{2-[(23-difluorophenyl)amino]-2-oxoethyl}-lfl'-pyrazol-3-yl)ammo]-quinazolin-7-
yl}oxy)propyl](butyl)amino]ethyl phosphate (400 mg, 50 % yield) as a pale yellow solid :
'H-NMR (CDC13) : 12.80 (br s, IH), 9.47 (br s, IH), 9.40 (br s, IH), 8.72 (s, IH), 8.13 (d,
IH), 8.05 (m, IH), 7.22 (s, IH), 7.18 (d, IH), 7.03 (m, IH), 6.86 (m, IH), 6.15 (br s, IH),
4.15 (t, 2H), 4.00 (q, 2H), 3.83 (s, 2H), 2.73 (t, 2H), 2.64 (t, 2H), 2.47 (t, 2H), 1.93 (m, 2H),
1.48 (s, 18H), 1.44 (m, 2H), 1.29 (m, 2H), 0.89 (t, 3H) :
MS (+ve ESI): 746 (M+H)+.

Example 35 - Preparation of compound 35 in table 3 - 2-{cyclopentylf3-({4-f(5-|2-f(2,3-difluorophenynamino1-2-oxoethvI}-lJ:r-Pvrazol-3-vI)amino]-quinazolin-7-yl}oxy)propvl]amino|ethyl dihvdrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino3-2-oxoethyl}-lH-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]amino) ethyl phosphate (405 mg, 0.53 mmol) yielded compound 35 in table 3 (388 mg, 100 % yield) as a pale yellow dihydrocbJoride salt: 'H-NMR (DMSO dg): 12.00 (s, 1H), 10.33 (s, 1H), 8.93 (s, 1H), 8.83 (d, 1H), 7.69 (m, 1H), 7.49 (d, 1H), 7.41 (s, 1H), 7.20 (m, 2H), 6.74 (s, 1H), 4.32 (t, 2H), 4.29 (m, 2H), 3.93 (s, 2H), 3.77 (m, 1H), 3.46 (m, 2H), 3.35 (m, 2H), 2.31 (m, 2H), 2.08 (m, 2H), 1.83 (m, 2H), 1.74 (m, 2H), 1.57(m,2H): MS (+ve ESI): 646 (M+H)+.
di-/e^butyl2-{cyclopentyl[3 a) An analogous reaction to that described in example 28f, but starting with 2-
(cyclopentylamino)ethanol (1.00 g, 7.75 mmol) yielded JV-(2,3-difluorophenyl)-2-{3-[(7-{3-
[cyclopentyl(2-hydroxyemyl)amino]propoxy}-quinazolm-4-yl)amino]-l/f-pyrazol-5-
yl}acetamide as a pale yellow solid (533 mg, 37 % yield) :
'H-NMR (DMSO d6) : 12.66 (s, 1H), 12.30 (s, 1H), 10.16 (m, 2H), 8.52 (m, 2H), 7.72 (m, 1H), 7.06-7.40 (m, 4H), 6.80 (s, 1H), 4.32 (m, 1H), 4.19 (t, 2H), 3.85 (br s, 2H), 3.43 (m, 2H), 3.06 (m, 1H), 2.66 (m, 2H), 2.56 (m, 2H), 1.90 (m, 2H), 1.73 (m, 2H), 1.58 (m, 2H), 1.48 (m, 2H), 1.32(m,2H): MS (+ve ESI): 566 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
" cyclopentyl(2-hydroxyethyl)amino]propoxy} -quinazolin-4-yl)amino] -1 #-pyrazol-5 -yl} -N-
'2,3-difluorophenyl)acetarnide (482 mg, 0.85 mmol) yielded di-tert-butyl 2-{cyclopentyl[3-
'{4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoemyl}-l^-pyrazol-3-yl)amino]-quinazolin-7-
^l}oxy)propyl]amino} ethyl phosphate (411 mg, 64 % yield) as a pale yellow solid :
H-NMR (CDC13): 12.70 (br s), 1H), 9.35 (m, 2H), 8.71 (s, 1H), 8.05 (m, 2H), 7.20 (s, 1H),
7.12 (d, 1H), 7.01 (m, 1H), 6.86 (m, 1H), 6.17 (br s), 1H), 4.11 (t, 2H), 3.98 (q, 2H), 3.83 (s,
2H), 3.08 (m, 1H), 2.80 (t, 2H)5 2.72 (t, 2H), 1.95 (m, 2H), 1.78 (m, 2H), 1.69 (m, 2H), 1.62
(m, 2H), 1.50 (s, 18H), 1.35 (m, 2H) :

MS (+ve ESI): 758 (M+H)+.
Example 36 - Preparation of Compound 36 in table 3 - I(2ty)-l-r3-f|4-r(5-|2-rf2.3-difluorophenvDaminol-l-oxoethylV-Lg-pyrazoI-S-yDaminol-quinazolin-?-yl}oxy)propvllpyrrolidin-2-yl|methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(tert-butyl) {(25)-l-[3 di(fer/-butyl) {(2lS)-l-[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^T-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with L-prolinol
(770 mg, 7.62 mmol) yielded ^-(233-difluorophenyl)-2-{3-[(7-{3-[(21S)-2-
(hydroxymethyl)pyrrolidin-1 -yljpropoxy } -quinazolin-4-yl)amino] -1 #-pyrazol-5 -
yl}acetamide as a pale yellow solid (547 mg, 40 % yield):
JH-NMR (DMSO d6) : 12.66. (s, 1H), 12.35 (s, 1H), 10.20 (m, 2H), 8.51 (m, 2H), 7.72 (m, IH), 7.20 (m, 4H), 6.77 (br s, 1H), 4.21 (t, 2H), 3.81 (br s, 2H), 3.47 (m, 1H), 2.90-3.42 (m, 6H), 2.05 (m, 2H), 1.90 (m, 1H), 1.72 (m, 2H), 1.62 (m, 1H) : MS (+ve ESI): 538 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 7V-(2,3-
difluorophenyl)-2-{3-[(7-{3-[(25)-2-(hydroxymethyl)pyrrolidin-l-yl]propoxy}-quinazolin-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (485 mg, 0.90 mmol) yielded di(ferf-butyl) {(21S)-l-[3-
({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-quinazolin-7-
yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (430 mg, 65 % yield) as a pale yellow solid :
'H-NMR (CDC13): 12.70 (br s, IH), 9.52 (br s, 1H), 9.37 (br s, 1H), 8.10 (s, 1H), 8.06 (m,
1H), 7.18 (s, IH), 7.11 (d, IH), 7.02 (m, IH), 6.85 (m, IH), 6.22 (br s, IH), 4.12 (m, 2H),

3.92 (m, IH), 3.84 (s, 2H), 3.68 (m, IH), 3.12 (m, IH), 2.97 (m, IH), 2.73 (m, IH), 2.48 (m, IH), 2.25 (q, IH), 1.85-2.05 (m, 3H), 1.55-1.85 (m, 3H), 1.45 (s, 18H): MS (+ve ESI) : 730 (M+H)+.
Example 37 - Preparation of Compound 37 in table 3 - K2^-l-r3-(l4-r(5-|2-rr3-fluorophenyl)amino]-2-oxoethvI|-lfl-pyrazol-3-yI)amino1-quinazolin-7-yI}oxv)propynpyrrolidin-2-yUmethvI dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(ferf-butyl) {(21y)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJH-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (654 mg, 0.92 mmol) yielded compound 37 in table 3 (596 mg, 97 % yield) as an off-white dihydrochloride salt:
'H-NMR (DMSO d6): 11.95 (s, m), 10.73 (s, IH), 8.94 (s, m), 8.82 (d, m), 7.65 (d, m),
7.46 (d, IH), 7.38 (m, 3H), 6.90 (m, IH), 6.74 (s, IH), 4.32 (t, 2H), 4.21 (m, 2H), 3.85 (s,
2H), 3.78 (m, IH), 3.64 (m, 2H), 3.29 (m, IH), 3.19 (q, IH), 2.31 (m, 3H), 2.20 (m, IH), 2.00
(ni,3H), 1.81(m, IH):
MS (+ve ESI) : 599.8 (M+H)+.
di(te/"/-butyl) {(21Sr)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-17/-pyrazol-3-
yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate used as starting
material was obtained as follows :
a) An analogous reaction to that described in example 28f, but starting with L-prolinol
(0.89 ml, 8.80 mmol) and 2-(3-{[7-(3-chloropropoxy)quinazolin-4-yl]amino}-lH-pyrazol-5-
yl)-7W(3-fluorophenyl)acetamide (1.00 g, 2.20 mmol) yielded 7V-(3-fluorophenyl)-2- {3-[(7-
{3-[(2iS)-2-(hydroxymethyl)pyrrolidin-1 -yljpropoxy} -quinazolin-4-yl)amino]-l #-pyrazol-5-
yl}acetamide as a cream solid (795 mg, 70 % yield) :
'H-NMR (DMSO d6): 12.35 (m, IH), 10.42 (s, IH), 10.19 (m, IH), 8.50 (s, 2H), 7.63 (d, IH), 7.35 (m, 2H), 7.16 (m, 2H), 6.90 (t, IH), 6.73 (m, IH), 4.28 (t, IH), 4.18 (t, 2H), 3.73 (s, 2H), 3.40 (m, IH), 3.20 (m, IH), 3.07 (m, IH), 2.97 (m, IH), 2.43 (m, 2H), 2.15 (q, IH), 1.94 (m, 2H), 1.81 (m, IH), 1.64 (m, 2H), 1.55 (m, IH) : MS (+ve ESI) : 520.1 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 7Y-(3-
fluorophenyl)-2-{3-[(7-{3-[(2)S)-2-(^ydroxymemyl)pyn:olidin-l-yl]propoxy}-quina2olin-4-
yl)ammo]-ltf-pyrazol-5-yl}acetarnide (730 mg, 1.41 mmol) yielded di(tert-butyl) {(25)-l-[3-
({4-[(5-{2-[(3-fluorophenyl)anuno]-2-oxoethyl}-17?-pyrazol-3-yl)amino]-quinazolin-7-

yl}oxy)propyl]pyrrolidin-2-yl} methyl phosphate (654 mg, 65 % yield) as a pale yellow solid
which was used in the next step without further characterisation.
2-(3- {[7-(3-chloropropoxy)quinazolin-4-yl]amino} - lfi"-pyrazol-5-yl)-7^-(3-
fluorophenyl)acetamide used as starting material was obtained as follows:
c) Pentafluorophenyl trifluoroacetate (23.25 g, 83 mmol) was added dropwise to a
solution of (3-{[7-(3-chloropropoxy)quina2oh^-4-yl]arnino}-l/f-pyrazol-5-yl)acetic acid
(15.0 g, 41 mmol) andpyridine (6.7 ml, 83 mmol) in dimethylformamide (150 ml) with
cooling to maintain the solution temperature at temperature for 30 minutes before addition of 3-fluoroaniline (9.22 g, 83 mmol). The reaction
was stirred for 2.5 hours at ambient temperature and then a further portion of 3-fluoroaniline
(2 ml) was added and the mixture was heated at 90°C for 3 hours. The reaction mixture was
poured into dilute hydrochloric acid (0.1 M) and ice (ca. 500ml) and the resultant solid was
filtered, washed with water and then diethyl ether and then dried to give 2-(3-{[7-(3-
chloropropoxy)quinazolin-4-yl]amino}-l#-pyrazol-5-yl)-N-(3-fluorophenyl)acetamide (17.7
g, 94% yield) as a brown solid :
'H-NMR (DMSO dc) : 12.50 (br s, 1H), 10.42 (s, 1H), 8.59 (s, 1H), 8.54 (d, 1H), 7.62 (m,
1H), 7.35 (m, 2H), 7.24 (m, 1H), 7.19 (m, 1H), 6.90 (m, 1H), 6.67 (br s, 1H), 4.28 (t, 2H),
3.84 (t, 2H), 3.76 (s, 2H), 2.27 (quintet, 2H).
MS (+ve ESI) : 455 (M+H)+.
Example 38 - Preparation of compound 38 in table 3 - 2-|cyclopentylf3-((4-f(5-|2-r(3-fluorophenyl)amino]-2-oxoethyl}-lg-pyrazol-3-yl)amino1-quinazolin-7-yUoxv)propyl1amino}ethyI dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{cyclopentyl[3-( {4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl}- lff-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (572 mg, 0.77 mmol) yielded compound 38 in table 3 (568 mg, 100 % yield) :
]H-NMR (DMSO d6): 11.95 (s, 1H), 10.73 (s, 1H), 8.94 (s, 1H), 8.82 (d, 1H), 7.65 (d, 1H), 7.48 (d, 1H), 7.38 (m, 3H), 6.89 (m, 1H), 6.75 (s, 1H), 4.30 (m, 4H), 3.85 (s, 2H), 3.78 (t, 1H), 3.47 (m, 2H), 3.37 (m, 2H), 2.60 (m, 2H), 2.08 (m, 2H), 1.78 (m, 4H), 1.56 (m, 2H) : MS (+ve ESI): 628.4 (M+H)+.

di-te^butyl2-{cyclopentyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-quinazoUn-7-yl}oxy)propyl]amino} ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 37a, but starting with 2-
(cyclopentylamino)ethanol (1.13 ml, 8.80 mmol) yielded 2-{3-[(7-{3-[cyclopentyl(2-
hyolroxyethyl)amino]propoxy}-quinazolm^-yl)aniino]-lJff-pyrazol-5-yl}-Ar-(3-
fluorophenyl)acetamide as a cream solid (620 mg, 51 % yield) :
'H-NMR (DMSO d6): 12.31 (m, m), 10.39 (s, m), 10.16 (m, m), s.so (s, 2H), 7.62 (d,
1H), 7.35 (m, 2H), 7.16 (m, 2H), 6.90 (t, 1H), 6.78 (m, 1H), 4.29 (m, 1H), 4.16 (t, 2H), 3.74 (s, 2H), 3.40 (m, 2H), 3.05 (t, 1H), 2.66 (t, 2H), 2.54 (obs m, 2H), 1.86 (t, 2H), 1.72 (m, 2H), 1.54 (m, 2H), 1.45 (m, 2H), 1.31 (m, 2H) : MS (+ve ESI) : 548.1 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 2- {3-[(7- {3-
[cyclopentyl(2-hydroxyethyl)ammo]propoxy}-qumazolin-4-yl)arrmio]-l/f-pyrazol-5-yl}-7v'-
(3-fluorophenyl)acetamide (580 mg, 1.06 mmol) yielded di-/er/-butyl 2-{cyclopentyl[3-({4-
[(5-{2-[(3-fluorophenyl)amino]-2-oxoemyl}-lH-pyrazol-3-yl)amino]-quinazolin-7-
yl}oxy)propyl]amino}ethyl phosphate (572 mg, 72 % yield) as a pale yellow solid which was
used in the next step without further characterisation.
Example 39 - Preparation of Compound 39 in table 3 - 2-fr3-(f4-rf5-(2-r(3-fluorophenyl)amino1-2-oxoethyl|-lg-pyrazoI-3-yl)amino1-quinazolin-7-yUoxy)propyn(ethyI)amino1 ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(ter/-butyl) 2-[[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoemyl}-lJ/~pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)propyl](ethyl)ammo]ethyl phosphate (539 mg, 0.77 mmol) yielded compound 39 in table 3 (504 mg, 99 % yield) as a pale yellow dihydrochloride salt:
'H-NMR (DMSO dg): 11.98 (s, 1H), 10.79 (s, 1H), 8.93 (s, 1H), 8.83 (d, 1H), 7.65 (d, 1H), 7.47 (d, 1H), 7.38 (m, 3H), 6.89 (t, 1H), 6.74 (s, 1H), 4.32 (t, 2H), 4.28 (m, 2H), 3.85 (s, 2H), 3.42 (m, 2H), 3.34 (m, 2H), 3.27 (q, 2H), 2.29 (m, 2H), 1.28 (t, 3H) : MS (+ve ESI): 587.8 (M+H)+.
di(to^butyl)2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoe%l}-lfl'-pyrazol-3-yl)ammo]-quinazolin-7-yl}oxy)propyl](ethyl)amino] ethyl phosphate used as starting material was obtained as follows :

a) An analogous reaction to that described in example 37a, but starting with 7V-
(ethylamino)ethanol (1.07 ml, 11.0 mmol) yielded 7V-(3-fluorophenyl)-2-{3-[(7-{3-[ethyl(2-
hydroxyethyl)amino]propoxy} -quinazolin-4-yl)amino]- l/f-pyrazol-5-yl} acetamide as a
yellow solid (660 mg, 59 % yield) :
'H-NMR (DMSO (fc) : 12.31 (m, IH), 10.39 (s, IH), 10.15 (m, IH), 8.51 (s, 2H), 7.62 (d, IH), 7.35 (m, 2H), 7.16 (m, 2H), 6.90 (t, IH), 6.78 (m, IH), 4.29 (m, IH), 4.20 (t, 2H), 3.76 (s, 2H), 3.45 (m, 2H), 3.30 (m, 4H), 2.61 (t, 2H), 1.89 (t, 2H), 0.95 (t, 3H): MS (+ve ESI): 508.4 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with 7V-(3-
fluorophenyl)-2-{3-[(7-{3-[ethyl(2-hydroxyethyl)ammo]propoxy}-quma2olm-4-yl)aniino]-
ltf-pyrazol-5-yl}acetamide (620 mg, 1.22 mmol) yielded di(fert-butyl) 2-[[3-({4-[(5-{2-[(3-
fluorophenyl)amino]-2-oxoethyl} - l#-pyrazol-3-yl)arnino]-quinazolin-7-
yl}oxy)propyl](ethyl)amino]ethyl phosphate (539 mg, 63 % yield) as a pale yellow solid
which was used in the next step without further characterisation.
Compound 39, synthesised above as the dihydrochloride salt, could also be prepared as the free base according to the following method:
c) An analogous reaction to that described in example 6d, but starting with Compound 39
yielded the free base of Compound 39 as a pale yellow solid:
'H-NMR (DMSO d6): 10.53 (s, IH), 8.57 (s, IH), 8.54 (d, IH), 7.62 (d, IH), 7.37 (m, 2H),
7.27 (s, IH), 7.21 (d, IH), 6.88 (m, IH), 6.65 (s, IH), 4.27 (t, 2H), 4.05 (m, 2H), 3.75 (s, 2H),
3.24 (m, 2H), 3.21 (t, 2H), 3.13 (q, 2H), 2.18 (m, 2H), 1.24 (t, 3H) :
MS (+ve ESI) : 588 (M+H)+.
C26H3iFN706P + 3.0 H2O requires C, 48.7%; H, 5.8%; N, 15.3%; Found C, 48.8%; H, 5.35%;
N, 15.15%.
Example 40 - Preparation of compound 40 in table 3 - 3-(r3-((4-f(5-|2-rr3-fluorophenyl)amino1-2-oxoethyI}-ljg-pyrazol-3-yl)amino1quinazolin-7-yl}oxy)propyl1amino)-3-methylbutyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 3-{[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-ll/-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino}-3-methylbutyl phosphate (247 mg, 0.35 mmol) yielded compound 40 in table 3 (235 mg, 100 % yield) as a pale yellow dihydrochloride salt:

'H-NMR (DMSO d6): 11.98 (s, 1H), 10.76 (s, 1H), 8.94 (s, 1H), 8.83 (d, 1H), 7.65 (d, 1H),
7.48 (d, 1H), 7.37 (m, 3H), 6.89 (t, 1H), 6.75 (s, 1H), 4.35 (t, 2H), 4.00 (q, 2H), 3.85 (s, 2H),
3.11 (m, 2H), 2.26 (m, 2H), 2.05 (t, 2H), 1.35 (s, 6H):
MS (+ve ESI) : 601.8 (M+H)+.
di-tert-butyl 3- {[3-({4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} -lff-pyrazol-3-
yl)amino]quinazolin-7-yl}oxy)propyl]amino}-3-methylbutylphosphate used as starting.
material was obtained as follows :
a) An analogous reaction to that described in example 37a, but starting with 3-amino-3-
methylbutan-1-ol (1.15 ml, 11.0 mmol) yielded JV-(3-fluorophenyl)-2-{3-[(7-{3-[(3-hydroxy-
l,l-dimethylpropyl)amino]propoxy}qumazolm-4-yl)ammo]-lff-pyrazol-5-yl}acetamide as a
pale yellow solid (310 mg, 27 % yield) :
'H-NMR CDMSO d6): 12.31 (m, m), 10.40 (m, m), s.so (m, 2H), 7.62 (d, m), 7.35 (m,
2H), 7.11 (m, 2H), 6.89 (t, 1H), 6.56 (m, 1H), 4.18 (t, 2H), 3.71 (s, 2H), 3.52 (t, 2H), 2.65 (t, 2H), 1.86 (m, 2H), 1.52 (t, 2H), 1.04 (s, 6H) : MS (+ve ESI) : 522.5 (M+H)+.
b) An analogous reaction to that described in example 6c, but starting with A^-(3-
fluorophenyl)-2-{3-[(7-{3-[(3-hydroxy-l,l-dimethylpropyl)arnino]propoxy}quinazolin-4-
yl)ammo]-l#-pyrazol-5-yl}acetamide (310 mg, 0.59 mmol) yielded di-tert-butyl 3-{[3-({4-
[(5-{2-[(3-fluorophenyl)arnino]-2-oxoemyl}-lH-pyrazol-3-yl)arriino]quinazolin-7-
yl}oxy)propyl]amino}-3-methylbutyl phosphate (247 mg, 58 % yield) as a pale yellow solid
which was used in the next step without further characterisation.
Example 41 - Preparation of compound 41 in table 3 - 2-fr3-(l4-f(5-|2-r(3-fluorophenyDaminol-l-oxoethyll-lfl-pyrazoI-S-yDaminol-qumazolin-?-yl}oxy)propyl](propyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-/ert-butyl 2-[[3-({4-[(5-{2-[(3-fluorophenyl)arnino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-qumazolin-7-yl}oxy)propyl](propyl)amino]ethyl phosphate (270 mg, 0.38 mmol) yielded compound 41 in table 3 (248 mg, 96 % yield) as a dihydrochloride salt:
'H-NMR (DMSO d6): 11.98 (s, 1H), 10.77 (s, 1H), 8.96 (s, 1H), 8.84 (d, 1H), 7.65 (d, 1H), 7.46 (d, 1H), 7.32-7.41 (m, 3H), 6.88 (m, 1H), 6.73 (s, 1H), 6.73 (s, 1H), 4.32 (t, 2H), 4.27 (t, 2H), 3.87 (s, 2H), 3.43 (t, 2H), 3.14 (m, 2H), 2.28 (m, 2H), 1.75 (rn, 2H), 0.94 (t, 3H) : MS (+ve ESI): 602 (M+H)+,

MS(-veESI):600(M-H)-.
di-te^butyl2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-yl)aniino]-quinazolin-7-yl}oxy)propyl](propyl)amino] ethyl phosphate used as starting material was obtained as follows :
a) An analogous reaction to that described in example 37a, but starting with 2-
(propylamino)ethanol (0.89 g, 8.6 mmol) yielded JV-(3-fluorophenyl)-2-{3-[(7-{3-[(2-
hydroxyetiiyl)(propyl)arnino]propoxy}-quinazolin-4-yl)ainino]-l/f-pyrazol-5-yl}acetarnideas
a pale yellow solid (480 mg, 32 % yield):
'H-NMR (DMSO-d6) : 12.30 (br s, IH), 10.38 (s, IH), 10.15 (br s, IH), 8.50 (s, 2H), 7.60 (d, IH), 7.34 (m, 2H), 7.15 (br s, 2H), 6.90 (dd, IH), 6.78 (br s, IH), 4.30 (br s, IH), 4.18 (t, 2H), 3.75 (s, 2H), 3.45 (s, 2H), 2.33-2.75 (m, 6H), 1.90 (t, 2H), 1.40 (m, 2H), 0.80 (m, 3H): MS (+ve ESI) : 522 (M+H)+, MS (-ve ESI): 520 (M-H)~.
b) An analogous reaction to that described in example 6c, but starting with N-(3-
fluorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(propyl)amino]propoxy} -quinazolin-4-
yl)amino]-l//-pyrazol-5-yl)acetamide (470 mg, 0.90 mmol) yielded di-fert-butyl 2-[[3-({4-
[(5- {2-[(3-fluorophenyl)amino] -2-oxoethyl} - l#-pyrazol-3-yl)arnino] -quinazolin-7-
yl}oxy)propyl](propyl)amino]ethyl phosphate (271 mg, 42 % yield) as a pale yellow solid :
'H-NMR (OMSO d6): 12.08 (br s, IH), 10.00 (s, IH), 9.89 (br s, IH), 8.53 (s, IH), 8.42 (d,
IH), 7.59 (d, IH), 7.34 (m, 2H), 7.17 (m, 2H), 6.84 (m, IH), 6.56 (br s, 1H)5 4.25 (t, 2H), 3.94
(m, 2H), 3.76 (s, 2H), 2.79 (t, 2H), 2.71 (t, 2H), 2.50 (t, 2H), 1.93 (m, 2H), 1.48 (m, 20H),
0.89 (t, 3H):
MS(+veESI):714(M+H)+, MS(-veESI):712(M-H)-.
Example 42 - Preparation of Compound 42 in table 3 - |(2J?)-l-r3-q4-f(5-(2-rr3-fluorophenvDaminol-Z-oxoethyll-lJy-pyrazol-S-yDaminol-quinazolin-?-yI}oxy)propynpyrroIidin-2-yl>methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(tert-butyl) {(2^)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-m-pyrazol-3-yl)ammo]-quinazolin-7-yl}oxy)propyl]pyrrolidui-2-yl}methyl phosphate (280 mg, 0.39 mmol) yielded compound 42 in table 3 (268 mg, 100 % yield) as a pale yellow dihydrochloride salt:

'H-NMR (DMSO dfi): 11.96 (s, IH), 10.75 (s, IH), 8.94 (s, IH), 8.82 (d, IH), 7.65 (d, IH),
7.43 (d, IH), 7.28-7.41 (m, 3H), 6.91 (m, IH), 6.71 (s, IH), 4.31 (t, 2H)5 4.20 (m, 2H), 3.86
(s, 2H), 3.77 (m, IH), 3.55-3.69 (m, 2H), 3.29 (m, IH), 3.17 (m, IH), 2.22-2.37 (m, 2H), 2.17
(m, IH), 2.04 (m, IH), 1.90 (m, IH), 1.79 (m, IH):
MS (+ve ESI): 600 (M+H)+,
MS (-ve ESI) : 598 (M-H)".
di(tert-butyl) {(2K)-1-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-
yl)amino]-quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate used as starting
material was obtained as follows :
a) An analogous reaction to that described in example 37a, but starting with D-prolinol
(0.87 g, 8.6 mmol) yielded 7V-(3-fluorophenyl)-2-{3-[(7-{3-[(2^)-2-(hydroxymethyl)-
pyrrolidin-l-yl]propoxy}-quinazolin-4-yl)amino]-l//-pyrazol-5-yl}acetamide as a pale yellow
solid (530 mg, 35 % yield) :
'H-NMR (DMSO-d6) : 12.33 (br s, IH), 10.38 (s, IH), 10.20 (br s, IH), 8.50 (s, 2H), 7.60 (d,
IH), 7.35 (m, 2H), 7.15 (s, 2H), 6.89 (dd, IH), 6.75 (br s, IH), 4.30 (br s, IH), 4.16 (t, 2H),
3.73 (s, 2H), 3.39 (m, IH), 3.19 (m, IH), 3.08 (m, IH), 2.98 (m, IH), 2.17 (m, IH), 1.95 (m,
2H), 1.80 (m, IH), 1.49-1.73 (m, 4H) :
MS (+ve ESI) : 520 (M+H)+,
MS (-ve ESI): 518 (M-H)'.
b) An analogous reaction to that described in example 6c, but starting with 7V-(3-
fluorophenyl)-2-{3-[(7-{3-[(2^)-2-(hydroxyrnethyl)pyrrolidin-l-yl]propoxy}-quinazolin-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (530 mg, 1.02 mmol) yielded di(tert-butyl) {(2R)-l-[3-
({4-[(5- {2-[(3 -fluorophenyl)amino]-2-oxoethyl} -1 H-pyrazol-3 -yl)amino] -quinazolin-7-
yl}oxy)propyl]pyrrolidin-2-yl}methyl phosphate (280 mg, 39 % yield) as a pale yellow solid :
MS (+ve ESI): 712 (M+H)+,
MS (-ve ESI): 710 (M-H)Example 43 - Preparation of compound 43 in table 3 - 3-fr3-ri4-r(5-(2-rr3-fluorophenyI)amino1-2-oxoethvl]-lJjr-pyrazol-3-yl)amino1-quinazolin-7-vUoxv)propyn(ethvI)amino1propyI dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-bntyl 3-[[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoemyl}-l//-pyrazol-3-yl)amino]-quinazolin-7-

yl}oxy)propyl](ethyl)amino]propyl phosphate (45 mg, 0.06 mmol) yielded compound 43 in
table 3 (36 mg, 95 % yield) as a pale yellow dihydrochloride salt :
'H-NMR (DMSO d6): 10.35 (brs, IH), 8.78-9.10 (m, 2H), 7.55-7.62 (m, IH), 7.42-7.50 (m,
2H), 7.28-7.40 (m, 2H), 6.80-6.87 (m, IH), 6.65-6.79 (br m, IH), 4.35 (t, 2H), 3.95-4.02 (m,
2H), 3.85 (s, 2H), 3.28 (t, 2H), 3.15-3.25 (m, 4H), 2.25-2.35 (m, 2H), 2.05-2.15 (m, 2H), 1.31
(t, 3H):
MS (+ve ESI) : 602 (M+H)+.
di-te/-/-butyl 3-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lff-pyrazol-3-yl)amino]-
quina2olin-7-yl}oxy)propyl](ethyl)amino]propyl phosphate used as starting material was
obtained as follows :
a) An analogous reaction to that described in example 37a, but starting with 3-
aminopropan-1-ol (247 mg, 3.3 mmol) yielded JV-(3-fluorophenyl)-2-{3-[(7-{3-[(3-
hyoVoxypropyl)amino]propoxy}quinazolm-4-yl)arnino]-lH-pyrazol-5-yl}acetamide as a pale
yellow solid (295 mg, 54 % yield) :
'H-NMR (DMSO ds) : 10.42 (br s, IH), 8.43-8.54 (m, 2H), 7.58-7.63 (m, IH), 7.29-7.38 (m, 2H), 7.11-7.18 (m, 2H), 6.84-6.91 (m, IH), 6.56-6.78 (brrn, IH), 4.18 (t, 2H), 3.72 (s, 2H), 3.45 (t, 2H), 2.67 (t, 2H), 2.58 (t, 2H), 1.84-1.95 (m, 2H), 1.51-1.61 (m, 2H) : MS (+ve ESI): 494 (M+H)+.
b) Tri(acetoxy)borohydride (750 nig, 1.48 mmol) was added to a solution of 7V-(3-
fluorophenyl)-2-{3-[(7-{3-[(3-hydroxypropyl)amino]propoxy}quinazolin-4-yl)amino]-lH'-
pyrazol-5-yl}acetamide (290 mg, 0.59 mmol) and acetaldehyde (39 mg, 0.88 mmol) in
dimethylformamide (3 ml) at ambient temperature and the reaction stirred for 2 hours. The
reaction mixture was filtered, diluted with dichloromethane (10 ml) and purified by flash
chromatography on silica gel, eluting with 3-12% methanol: dichloromethane. Evaporation of
the fractions in vacua yielded 2-{3-[(7-{3-[ethyl(3-hydroxypropyl)amino]propoxy}-
quinazolin-4-yl)amino]-lH-pyrazol-5-yl}-JV-(3-fluorophenyl)acetamide (105 mg, 34 % yield)
as a white solid :
'H-NMR (DMSO d6): 10.41 (br s, IH), 10.13-10.30 (br s, IH), 8.43-8.55 (m, 2H), 7.57-7.65 (m, IH), 7.28-7.39 (in, 2H), 7.09-7.21 (m, 2H), 6.83-6.92 (m, IH), 6.65-6.81 (m, IH), 4.15 (t, 2H), 3.73 (s, 2H), 3.41 (t, 2H), 2.41-2.58 (m, 6H under DMSO), 1.82-1.93 (m, 2H), 1.48-1.58 (m, 2H), 0.94 (t, 3H): MS (+ve ESI): 522 (M+H)+.

c) An analogous reaction to that described in example 6c3 but starting with 2- {3-[(7-{3-
[emyl(3-hydroxypropyl)ammo]propoxy}quinazolm-4-yl)arm^
fluorophenyl)acetamide (90 mg, 0.17 rnmol) yielded di-tert-butyl 3-[[3-({4-[(5-{2-[(3-
fluorophenyl)amino]-2-oxoe1iiyl}-17?-pyrazol-3-yl)arnino]-quinazolin-7-
yl}oxy)propyl](ethyl)amino]propyl phosphate (45 mg, 37 % yield) as a pale yellow solid :
MS(+veESI):714(M+H)+,
MS(-veESI):712(M-H)~.
Example 44 - Preparation of compound 44 in table 3 - 2-rf3-((4-f(5-{2-f(3-fluorophenvl)amino1-2-oxoethyI}-lflr-pyrazol-3-yl)aminolquinazolin-7-yI}oxy)propynf2-methoxyethyl)amino]ethyl dihydrogen phosphate
Di-/errtutyl2-[[3-({4-[(5-{2-[(3-iluorophenyl)amino]-2-oxoethyl}-l/?-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl](2-methoxyethyl)amino]ethyl phosphate (200 mg, 0.3 mmol) was solubilised in dioxane (7 ml) and treated with a mixture of dioxane/hydrochloric acid (4.0 N, 0.5 ml) at 20 °C overnight. A light yellow solid was recovered by filtration and dried in vacua (55 °C, 12 h) to yield 2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-1 F-pyrazol-S-yl)amino]quinazolin-7-yl} oxy)propyl] (2-methoxyethyl)amino] ethyl dihydrogen phosphate (200 mg, 85 % yield) as a pale yellow solid :
1H-NMR (DMSO d& CH3COOD) : 8.95 (s, 1H), 8.82 (d, 1H), 7.65 (d, 1H), 7.46 (d, IE), 7.37 (m, 3H), 6.88 (m, 1H), 6.78 (s, 1H), 4.33 (m, 2H), 4.28 (m, 2H), 3.86 (s, 2H), 3.76 (m, 2H), 3.53 (m, 2H), 3.45 (m, 4H), 3.34 (s, 3H), 2.30 (m, 2H) : MS (+ve ESI): 618 (M+H)+.
di-fcrt-buryl 2-[[3-( {4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} - lH-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl](2-methoxyethyl)amino]ethyl phosphate used as starting material, was obtained as follows:
a) 2-((2-methoxyethyl)amino)ethanol (750 mg, 6.29 mmol) was added to a solution of 2-(3-{[7-(3-chloropropoxy)quinazolin-4-yl]arnino}-lH"-pyrazol-5-yl)-Ar-(3-fluorophenyl)acetamide (960 mg, 2.11 rnniol) and potassium iodide (700 mg, 4.22 mmol) in l-methyl-2-pyrrolidinone (8 ml). The mixture was stirred at 80 °C for 1.5 hours, cooled, added onto a silica gel column, and purified by chromatography eluting successively with dichloromethane, dichloroniethane: methanol 96: 4 to 92: 8 to give A^-(3-fluorophenyl)-2-{3-[(7-{3-[(2-hydroxyethyl)(2-methoxyethyl)arnino]propoxy}qumazolin-4-yl)amuio]-l/:/-pyrazol-5-yl}acetarnide (600 mg, 53 % yield) as an off white solid.

'H-NMR (DMSO d6, TFA): 9.0 (s, IH), 8.83 (d, IH), 7.65 (d, IH), 7.48 (d, IH), 7.36 (m, 2H), 7.28 (s, IH), 6.88 (m, IH), 6.80 (s, IH), 4.32 (m, 2H), 3.86 (s, 2H), 3.80 (m, 2H), 3.73 (m, 2H), 3.48 (m, 4H), 3.37 (m, 2H), 3.34 (s, 3H), 2.28 (m, 2H) : MS (+ve ESI) : 538 (M+H)+.
b) Di-tert-butyl-diethylphosphoramidite (0.56 ml, 2 mmol) was slowly added to a mixture of A^-(3-fluorophenyl)-2- {3-[(7- {3-[(2-hydroxyethyl)(2-
methoxyethyl)amino]propoxy}quinazolm-4-yl)amino]-lI7-pyrazol-5-yl}acetaniide (540 mg, 1 mmol) and tetrazole (200 mg, 3 mmol) in dimethylformamide (5 ml) at 20 °C for 2 hours. The mixture was then cooled to 0 °C and hydrogen peroxide (9.0 N, 0.33 ml, 2.93 mmol) was slowly added and stirring at ambient temperature was continued for 12 hours. Sodium metabisulphite (1.14 g, 6 mmol) in solution in water (12 ml) was then added to the reaction mixture at 0°C, which was slowly allowed to warm to ambient temperature. The solvents were then evaporated and the residue was purified by silica gel chromatography, eluting with dichloromethane: methanolic ammonia (3.0 N) 96: 4 to 94: 6 to yield di-te/-/-butyl 2-[[3-({4-[(5-{2-[(3-fluorophenyl)aniino]-2-oxoethyl}-lJHr-pyrazol-3-yl)arnino]quinazolm-7-yl}oxy)propyl](2-methoxyethyl)amino]ethyl phosphate (220 mg, 30 % yield) :
'H-NMR (DMSO d6, TFA) : 8.98 (s, m), s.si (d, m), 7.63 (d, IH), 7.48 (d, m), 7.36 (m,
2H), 7.27 (s, IH), 6.90 (t, IH), 6.77 (s, IH), 4.30 (m, 2H), 4.26 (m, 2H), 3.84 (s, 2H), 3.72 (m, 2H), 3.55 (m, 2H), 3.48 (m, 2H), 3.42 (m, 2H), 3.34 (s, 3H), 2.26 (m, 2H), 1.44 (s, 18H): MS (+ve ESI) : 730 (M+H)+.
Example 45 - Preparation of compound 45 in table 4 - 2-fr4-(|4-f(5-|2-r(2,3-difluorophenyI)amino|-2-oxoethyl|-lfl-pyrazoI-3-yl)amino]-quinazoIin-7-vl}ory)butvn(propyl)amino] ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-ter/-butyl 2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoemyl}-lJ?-pyrazol-3-yl)ainino]-quuiazolin-7~yl}oxy)butyl](propyl)amino]ethyl phosphate (550 mg, 0.74 mmol) yielded compound 45 in table 4 (504 mg, 96 % yield) as the dihydrochloride salt:
'H-NMR (DMSO d6): 11.95 (s, m), 10.34 (s, IH), 8.90 (s, m), 8.83 (d, IH), 7.68 (m, m),
7.45 (m, 2H), 7.22 (m, 2H), 6.72 (s, IH), 4.23 (m, 4H), 3.91 (s, 2H), 3.40 (m, 2H), 3.20 (m, 2H), 3.08 (m, 2H), 1.88 (m, 4H), 1.71 (m, 2H), 0.90 (t, 3H): MS (+ve ESI): 634 (M+H)+, MS (-ve ESI) : 632 (M-H)".

di-/e;Y-butyl2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amiino]-2-oxoethyl}-lF-pyrazol-3-yl)ammo]-qumazolm-7-yl}oxy)butyl](propyl)arnino]ethyl phosphate used as starting material was obtained as follows :
a) 1,4-Dihydroxybutane (33.0 ml, 366 mmol) was added over 10 minutes to a stirred suspension of sodium hydride (14.6 g of a 60% dispersion in oil, 366 mmol) in dimethylacetarnide (200 ml) at 0 °C and the reaction stirred for 15 minutes before being heated to 60 °C. A solution of 7-fluoroquinazolin-4(3H)-one (10.0 g, 61.0 mmol) in dimethylacetamide (60 ml) was added over 5 minutes and the reaction stirred at 110 °C for a further 5 hours. The reaction was cooled, poured onto ice (500 g) and treated with brine (500 nil) and 5.0 N hydrochloric acid (until pH b) Dimethylformamide (0.5 ml) was added to a stirred suspension of 7-(4-hydroxy-butoxy)quinazolin-4(3.ff)-one (4.86 g, 20.0 mmol) in thionyl chloride (50 ml) and the reaction heated at reflux for 1 hour. The reaction was cooled, the excess thionyl chloride was evaporated in vacua and the residue was azeotroped with toluene (2 x 50 ml) before being taken up in dimethylacetarnide (50 ml). 5-amino-lH-pyrazole-3-acetic acid (2.82 g, 20 mmol) and 4.0 N hydrochloric acid in dioxan (5.0 ml, 20 mmol) were added and the reaction was stirred at 90 °C for 40 minutes. The reaction was cooled to ambient temperature, poured into ice-water (500 ml) and acidified to pH >12 with 40% aqueous sodium hydroxide solution. The reaction was filtered, the filtrate was acidified to pH 'H-NMR (DMSO d6): 12.45 (br s, 2H), 8.57 (s, m), 8.50 (d, m), 7.17 (m, 2H), 6.60 (s, m),
4.18 (m, 2H), 3.75 (m, 2H), 3.65 (s, 2H), 1.90 (m, 4H) :
MS(+veESI):376(M+H)+,
MS (-ve ESI) : 374 (M-H)'.

c) Phosphorus oxychloride (1.8 ml, 19.5 mmol) was added to a stirred suspension of 2,3-difluoroaniline (2.88 g, 22.3 mmol), (3-{[7-(4-chlorobutoxy)quinazolin-4-yl]amino}-lH-pyrazol-5-yl)acetic acid (6.97 g, 18.6 mmol) and pyridine (100 ml) at 0 °C. The reaction was stirred for 2.5 hours at 0 °C, additional phosphorus oxychloride (0.3 ml) was added and the reaction allowed to warm to ambient temperature over 18 hours. Ethyl acetate (200 ml) and diethyl ether (100 ml) were added, the reaction was stirred and the sticky solid collected by filtration before being suspended in water (300 ml). Dilute aqueous ammonia was added until the pH was >7 and the resultant solid was collected by suction filtration. Washing of the resultant solid with water and then acetonitrile, followed by prolonged drying in vacua, yielded 2-(3-{[7-(4-chlorobutoxy)quinazolin-4-yl]amino}-lff-pyrazol-5-yl)-JV-(2,3-difluorophenyl)acetamide (7.6 g, 84 % yield) as a pale brown solid : 'H-NMR (DMSO d d) An analogous reaction to that described in example 28f, but starting with 2-
(propylamino)ethanol (765 mg, 7.40 mmol) and 2-(3-{[7-(4-chlorobutoxy)quinazolin-4-
yl]amino}-lJff-pyrazQl-5-yl)-JV-(2,3-difluorophenyl)acetamide (1.20 g, 2.47 mmol) yielded N-
(2,3-difluorophenyl)-2- {3-[(7- {4-[propyl(2-hydroxyethyl)amino]butoxy} -quinazolin-4-
yl)arnino]-lH-pyrazol-5-yl}acetamide as a brown solid (625 mg, 46 % yield) :
]H-NMR (DMSO d6) : 10.3 (br s, 1H), 8.49 (s, 1H), 8.45 (m, 1H), 7.70 (m, 1H), 7.15 (m, 3H), 7.1 (s, 1H), 6.58 (br, s, 1H), 4.1 (m, 2H), 3.80 (s, 2H), 3.42 (m, 2H), 2.45 (m, 4H), 2.33 (m, 2H), 1.77 (m, 2H), 1.55 (m, 2H), 1.35 (m, 2H), 0.81 (t, 3H): MS (+ve ESI): 554 (M+H)+ MS (-ve ESI): 552 (M-H)".
e) An analogous reaction to that described in example 6c, but starting with N-(2,3-
difluorophenyl)-2- {3-[(7- {4-[(2-hydroxyethyl)(propyl)amino]butoxy} -quinazolin-4-
yl)amino]-17?-pyrazol-5-yl}acetamide (540 mg, 0.98 mmol) yielded di-tert-butyl 2-[[4-({4-
[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoemyl}-l/ir-pyrazol-3-yl)aniino]-quinazolin-7-
yl}oxy)butyl](propyl)amino]ethyl phosphate (566 mg, 78 % yield) as a pale yellow solid:
'H-NMR (DMSO d6) : 12.3 (s, 1H), 10.18 (m, 2H), 8.51 (m, 2H), 7.72 (m, 1H), 7.15 (m, 4H),
6.77 (s, 1H), 4.15 (m, 2H), 3.85 (m, 4H), 2.65 (rn, 2H), 2.40 (m, 2H), 1.78 (m, 2H), 1.56 (m,
2H), 1.4 (m, 2H), 1.39 (s, 18H), 0.85 (t, 3H) :

MS (+ve ESI): 746 (M+H)+ MS (-ve ESI): 744 (M-H)".
Example 46 - Preparation of Compound 46 in table 4 - 2-rr4-f(4-r(5-|2-[(2.3-difluorophenyl)amino1-2-oxoethvI}-lfl-pyrazol-3-yl)aminol-quinazoIin-7-yUoxy)butyl1(ethyI)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(fert-butyl) 2-[[4-({4-[(5-{2-[(2J3-difluorophenyl)ammo]-2-oxoe%l}-lH-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)butyl](ethyl)amino]ethyl phosphate (386 mg, 0.53 mmol) yielded compound 46 in table 4 (340 mg, 93 % yield) as a white dihydrochloride salt: 'H-NMR (OMSO d6): H.97 (s, 1H), 10.35 (s, 1H), 8.92 (s, 1H), 8.85 (d, 1H), 7.67 (m, 1H), 7.45 (m, 2H), 7.18 (m, 2H), 6.75 (s, 1H), 4.23 (m, 4H), 3.90 (s, 2H), 3.39 (m, 2H), 3.20 (m, 4H), 1.87 (m, 4H), 1.25 (t, 3H) : MS(+veESI):619(M+H)+ MS(-veESI):617(M-H)-.
di(fe^butyl)2-[[4 a) An analogous reaction to that described in example 45d, but starting with 2-
(ethylamino)ethanol (468 mg, 5.25 mmol) yielded7V-(2,3-difluorophenyl)-2-{3-[(7-{4-
[ethyl(2-hydroxyethyl)amino]butoxy} -quinazolin-4-yl)amino]- l.ff-pyrazol-5-yl} acetamide as
an off-white solid (443 mg, 47 % yield):
'H-NMR (DMSO dg) : 10.25 (br s, 1H), 8.45 (m, 2H), 7.70 (m, 1H), 7.12 (m, 4H), 6.58 (br s,
1H), 4.25 (br s, 1H), 4.13 (m, 2H), 3.80 (s, 2H), 3.42 (m, 2H), 1.76 (m, 2H), 1.55 (m, 2H),
0.95 (t, 3H):
MS (+ve ESI) : 540 (M+H)+
MS (-ve ESI): 538 (M-H)'.
b) An analogous reaction to mat described in example 6c, but starting with A^-(2,3-
difluorophenyl)-2-{3-[(7-{4-[emyl(2-hydroxyemyl)amino]butoxy}-qumazolm-4-yl)arnino]-
lff-pyrazol-5-yl}acetamide (385 mg, 0.71 mmol) yielded di(te/-f-butyl) 2-[[4-({4-[(5-{2-[(2,3-
difluorophenyl)ammo]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-quinazolin-7-
yl}oxy)butyl](ethyl)amino]ethyl phosphate (393 mg, 75 % yield) as a pale yellow solid:

'H-NMR (DMSO d6): 12.30 (s, IH), 10.18 (br s, IH), 8.50 (m, 2H), 7.71 (m, IH), 7.15 (m,
4H), 6.78 (s, 1H), 4.3 (m, 2H), 3.85 (m, 4H), 2.68 (m, 2H), 1.78 (m, 2H), 1.58 (m, 2H), 1.40
(s, 18H),0.97(t,3H):
MS (+ve ESI) : 732 (M+H)+
MS (-ve ESI): 730 (M-HJ.
Example 47 - Preparation of Compound 47 in table 4 - ((2J?)-l-r4-f(4-f(5-(2-ff2,3-difluorophenvl)amino1-2-oxoethyl>-lg-pyrazoI-3-yl)amino]-quinazolin-7-yI|o;xy)butyl1pvrrolidin--2-vI}methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(te7-?-butyl) {(2^)4-[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoe%l}-lH-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)butyl]pyrrolidin-2-yl}methyl phosphate (464 mg, 0.62 mmol) yielded compound 47 in table 4 (400 mg, 91 % yield) as an off-white dihydrochloride salt:
'H-NMR (DMSO dg): 11.95 (s, IH), 10.35 (s, IH), 8.92 (s, m), s.ss (d, m), 7.68 (m, m),
7.45 (m, 2H), 7.18 (m, 2H), 6.71 (s, IH), 4.2 (m, 4H), 3.92 (s, 2H), 3.72 (m, IH), 3.60 (m,
IH), 3.45 (m, IH), 3.15 (m, 2H), 2.15 (m, IH), 1.7-2.1 (m, 7H) :
MS(+veESI):631(M+H)+
MS (-ve ESI) :630 (M-H)'.
di(ter/-butyl) {(2R)-1 -[4-( {4-[(5- {2-[(2,3-difluorophenyl)aniino]-2-oxoethyl} - l#-pyrazol-3-
yl)amino]-quinazolin-7-yl}oxy)butyl]pyrrolidin-2-yl} methyl phosphate used as starting
material was obtained as follows :
a) An analogous reaction to that described in example 45d, but starting with D-prolinol
(530 mg, 5.25 mmol) yielded7V-(2,3-difluorophenyl)-2-{3-[(7-{4-[(2J?)-2-
(hydroxyrnethyl)pyrrolidin-1 -yljbutoxy} -quinazolin-4-yl)amino]- l#-pyrazol-5-yl} acetarnide
as an off-white solid (516 mg, 54 % yield) :
'H-NMR (DMSO d6): 10.25 (br s, IH), 8.45 (m, 2H), 7.7 (m, IH), 7.15 (m, 4H), 6.6 (br s, IH), 4.30 (br s, IH), 4.21 (m, 2H), 3.80 (s, 2H), 3.40 (m, IH), 3.20 (m, IH), 3.05 (m, IH), 2.85 (m, IH), 2.40 (m, IH), 2.30 (m, IH), 2.10 (m, IH), 1.77 (m, 3H), 1.6 (m, 5H): MS (+ve ESI): 552 (M+H)+ MS (-ve ESI): 550 (M-H)~.
b) An analogous reaction to that described in example 6c, but starting with 7V-(2,3-
difluorophenyl)-2-{3-[(7-{4-[(2^)-2-(hydroxyrnethyl)pvrrolidin-l-yl]butoxy}-quinazoliii-4-
yl)amino]-l#-pyrazol-5-yl}acetamide (450 mg, 0.82 mmol) yielded di(te/-/-butyl) {(2/?)-l-[4-

({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoethyl}-lH-pyrazol-3-yl)ainino]-quinazolin-7-yl}oxy)butyl]pyrrolidin-2-yl}methyl phosphate (470 mg, 77 % yield) as a pale yellow solid :
'H-NMR (DMSO d6): 12.3 (s, m), 10.18 (s, m), 8.50 (m, 2H), 7.71 (m, m), 7.18 (m, 4H),
6.77 (s, 1H), 4.15 (m, 2H), 3.80 (m, 3H), 3.62 (m, 1H), 3.05 (m, 1H), 2.80 (m, 1H), 2.65 (m, 1H), 2.37 (m, 1H), 2.18 (m, 1H), 1.80 (m, 3H), 1.62 (m, 5H), 1.38 (s, 18H) : MS (+ve ESI): 744 (M+H)+ MS (-ve ESI): 742 (M-H)'.
Example 48 - Preparation of compound 48 in table 4 - 2-[[4-({4-r(5-|2-r(2,3-difluorophenYl)aminol-2-oxoethyl|-lJHr-pyrazoI-3-vl)amino1quinazoIin-7-vUoxv)butvn(methyl)amino1ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)aniino]-2-oxoethyl}-lJ:Z-pyrazol-3-yl)aniino]quinazolin-7-yl}oxy)butyl](methyl)amino]ethyl phosphate (250 mg, 0.35 mmol) yielded compound 48 in 5 table 4 (263 mg, 100 % yield) as an off-white dihydrochloride salt:
JH-NMR (DMSO d6): 11.95 (s, 1H), 10.35 (s, 1H), 8.92 (s, 1H), 8.83 (d, 1H), 7.69 (rn, 1H), 7.45 (m, 2H), 7.29 (m, 2H), 6.75 (s, 1H), 4.22 (m, 4H), 3.81 (s, 2H), 3.39 (m, 2H), 3.20 (m,
2H), 2.80 (s, 3H), 1.85 (m, 4H) :
MS (+ve ESI): 605 (M+H)+ I MS (-ve ESI): 603 (M-H)'.
di-to'/-butyl2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino].-2-oxoethyl}-l^-pyrazol-3-
yl)aniino]quinazolin-7-yl}oxy)butyl](methyl)amino] ethyl phosphate used as starting material
was obtained as follows :
a) An analogous reaction to that described in example 45d, but starting with 2-
(methylamino)ethanol (394 mg, 5.25 mmol) yielded N-(2,3-difluorophenyl)-2-{3-[(7-{4-[(2-
hydroxyethyl)(methyl)amino]butoxy}quinazolin-4-yl)amino]-lZf-pyrazol-5-yl)acetamide as
an off-white solid (536 mg, 58 % yield):
'H-NMR (DMSO d6): 10.25 (br s, 1H), 8.45 (m, 2H), 7.71 (m, 1H), 7.15 (m, 4H), 6.58 (br s,
1H), 4.3 (br s, 1H), 4.12 (m, 2H), 3.80 (s, 2H), 3.45 (m, 2H), 2.39 (m, 4H), 2.15 (s, 3H), 1.79
(m,2H), 1.58(m,2H):
MS (+ve ESI): 526 (M+H)+
MS (-ve ESI): 524 (M-H)".

b) An analogous reaction to that described in example 6c, but starting with ]V-(2,3-difluorophenyl)-2-{3-[(7-{4-[(2-hydroxyethyl)(methyl)amino]butoxy}quinazolin-4-yl)amino]-l#-pyrazol-5-yl}acetamide (460 ing, 0.88 mmol) yielded di-tert-butyl 2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)butyl](methyl)amino]ethyl phosphate (368 mg, 59 % yield) as a pale yellow solid : 'H-NMR (DMSO d6): 12.30 (s, IH), 10.17 (m, 2H), 8.50 (m, 2H), 7.70 (m, IH), 7.18 (m, 4H), 6.77 (s, IH), 4.15 (m, 2H), 3.9 (m, 2H), 3.85 (s, 2H), 2.60 (m, 2H), 2.43 (m, 2H), 2.20 (s, 3H), 1.8 (m, 2H), 1.58 (m, 2H), 1.40 (s, 18H) : MS (+ve ESI) : 718 (M+H)+ MS(-veESI): 716 (M-H)".
Example 49 - Preparation of Compound 49 in table 4 - {(2^-l-f4-(l4-rf5-(2-rf2,3-difluorophenyI)aininol-2-oxoethyl|-lff-pyrazol-3-yI)ainino1-quinazolin-7-yl}oiy)butyl1pyrrolidin-2-vI}methyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di(tert-butyl) {(26)-l-[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lfl-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)butyl]pyrrolidin-2-yl}methyl phosphate (386 mg, 0.53 mmol) yielded compound 49 in table 4 (340 mg, 93 % yield) as an off-white dihydrochloride salt:
'H-NMR (DMSO d6).-11,7 (br s, m), 10.30 (s, m), 8.87 (s, m), 8.75 (d, IH), 7.68 (m, IH),
7.40 (m, 2H), 7.19 (m, 2H), 6.71 (s, IH), 4.20 (m, 2H), 4.18 (m, 2H), 3.90 (s, 2H), 3.7 (m,
IH), 3.58 (m, IH), 3.42 (m, IH), 3.1 (m, 2H), 2.15 (m, IH), 1.75 - 2.1 (m, 7H) :
MS (+ve ESI) : 630 (M+H)+
MS (-ve ESI) : 632 (M-H)".
di(ter?-butyl){(25)-l-[4-({4-[(5-{2-[(2,3-difluorophenyl)ammo]-2-oxoethyl}-l^-pYrazol-3-
yl)amino]-quinazolin-7-yl}oxy)butyl]pyrrolidin-2-yl}memyl phosphate used as starting
material was obtained as follows :
a) An analogous reaction to that described in example 45d, but starting with L-prolinol
(530 mg, 5.25 mmol) yielded A^-(2,3-difluorophenyl)-2-{3-[(7-{4-[(26)-2-
(hydroxymethy^pyn-olidm-l-ylJbutoxyJ-quinazolin^-y^aminoJ-l/f-pyrazol-S-ylJacetamide
as an off-white solid (550 rng, 57 % yield):
'H-NMR (DMSO dfi): 12.38 (br s, IH), 10.20 (br s, IH), 8.47 (m, 2H), 7.70 (m, IH), 7.15 (m,
4H), 6.62 (br s, IH), 4.28 ( br s, IH), 4.15 (m, 2H), 3.81 (s, 2H), 3.40 (m, IH), 3.20 (m, IH),

3.02 (m, IH), 2.81 (m, IH), 2.38 (m, IH), 2.30 (m, 1H), 2.10 (m, IH), 1.78 (m, 3H), 1.58 (m,
5H):
MS (+ve ESI): 552 (M+H)+
MS (-ve ESI): 550 (M-H)'.
b) An analogous reaction to that described in example 6c, but starting with 7Y-(2,3-
difluorophenyl)-2- {3-[(7- {4-[(2jS)-2-(hydroxymethyl)pyn-olidin-1 -yljbutoxy} -quinazolin-4-
yl)arnino]-lfl"-pyrazol-5-yl}acetamide (340 mg, 0.62 mmol) yielded di(rerr-butyl) {(25)-l-[4-
({4-[(5-{2-[(2,3-difluorophenyl)animo]-2-oxoemyl}-l^f-pyrazol-3-yl)arnino]-quinazolin-7-
yl}oxy)butyl]pyrrolidin-2-yl}methyl phosphate (328 mg, 71 % yield) as a pale yellow solid :
'H-NMR (DMSO dfi): 12.30 (br s, IH), 10.15 (s, 2H), 8.48 (m, 2H), 7.68 (m, IH), 7.15 (m,
4H), 6.75 (br s, IH), 4.12 (m, 2H), 3.80 (m, 2H), 3.61 (m, IH), 3.05 (m, IH), 2.80 (m, IH),
2.62 (m, IH), 2.35 (m, IH), 2.15 (m, IH), 1.81 (m, 3H), 1.60 (m, 5H), 1.38 (s, 18H) :
MS (+ve ESI) : 744 (M+H)+
MS (-ve ESI): 742 (M-H)'.
Example 50 - Preparation of Compound 50 in table 5 - 2-(ethvir3-q6-fluoro-4-ff5-|2-r(3-fluorophenyDaminol-I-oxoethyll-ljg-pyrazol-S-yDaminolquinazolin-?-yl}oxy)propynamino|ethyl dihydrogen phosphate
An analogous reaction to that described in example 1, but starting with di-tert-butyl 2-{ethyl[3-({6-fluoro-4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH'-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino}ethyl phosphate (275 mg, 0.38 mmol) yielded compound 50 in table 5 (260 mg, 100 % yield) as an off-white dihydrochloride salt: 'H-NMR (DMSO d cU-/er^butyl2-{ethyl[3-({6-fluoro-4-[(5-{2-[(3-fluorophenyl)arriino]-2-oxoethyl}-lJ?:r-pyrazol-3-yl)amino]quinazolin-7-yl}oxy)propyl]amino}ethyl phosphate phosphate used as starting material was obtained as follows :
a) Benzyl alcohol (4.27 g, 39.5 mmol) was added dropwise to a stirred suspension of sodium hydride (1.6 g of a 60 % dispersion in mineral oil, 40.0 mmol) in dimethylformamide (50 ml) at 0 °C. The reaction was stirred at 0 °C for 1 hour before addition of 6,7-difluoroquinazolin-4(l.?f)-one (3.60 g, 19.8 mmol) whereupon the reaction was heated to 60

°C for 2 hours. The reaction was cooled to ambient temperature, poured into water (200 ml) and the resultant solid collected by suction filtration. Drying of the solid in vacua yielded 7-(benzyloxy)-6-fluoroquinazolhi-4(lJff)-one (4.45 g, 83 % yield) as a pale brown solid: 'H-NMR (DMSO dfi): 12.24 (br s, IH), 8.05 (s, IH), 7.80 (d, IH), 7.52 (m, 2H), 7.44 (m, ! 3H), 7.38 (t, 1H), 5.35 (s, 2H).
b) 7-(Benzyloxy)-6-fluoroquinazolin-4(lfi)-one (2.00 g, 7.41 mmol) was taken up in
phosphorus oxychlonde (20 ml) and the reaction heated at reflux for 90 minutes. The reaction
was cooled, azeotroped with toluene (2 x 50 ml) and taken up in dichloromethane (5 ml) The
organic phase was washed with saturated aqueous sodium hydrogen carbonate solution and
thend ried over magnesium sulphate. Solvent evaporation in vacua followed by drying of the
solid in vacua yielded 7-(benzyloxy)-4-chloro-6-fluoroquinazoline (1.50 g, 71 % yield) as a
pale yellow solid:
'H-NMR (CDC13) : 8.93 (s, IH), 7.89 (d, 1H), 7.51 (m, 3H), 7.35-7.46 (m, 3H), 5.32 (s, 2H).
c) A mixture of 7-(benzyloxy)-4-chloro-6-fluoroquinazoline (1.20 g, 4.16 mmol) and 2-
(3-amino4#-pyrazol-5-yl)-7V-(3-fluorophenyl)acetamide (0.97 g, 4.15 mmol) were heated at
reflux in 2-propanol (20 ml) for 2 hours. The reaction was cooled to ambient temperature,
diluted with diethyl ether and the resultant solid collected by suction filtration. Prolonged
drying in vacua yielded 2-(3-{[7-(benzyloxy)-6-fluoroquniazolin-4-yl]amino}-lI/'-pyrazol-5-
yl)-JV-(3-fluorophenyl)acetamide (2/.00 g, 92 % yield) as a pale yellow solid :
!H-NMR (DMSO dfi): 11.72 (br s, IH), 10.71 (s, IH), 8.90 (s, IH), 8.82 (d, IH), 7.65 (m, 2H), 7.55 (m, 2H), 7.32-7.50 (m, 5H), 6.89 (m, IH), 6.76 (s, IH), 5.42 (s, 2H), 3.84 (s, 2H): MS (+ve ESI): 487 (M+H)+.
d) A solution of 2-(3- {[7-(benzyloxy)-6-fluoroquinazolin-4-yl]amino}-l.ff-pyrazol-5-
yl)-7V-(3-fluorophenyl)acetamide (hydrochloride salt) (1.95 g, 3.74 mmol) in trifluoroacetic
acid (20 ml) was heated at reflux for 7 hours. The reaction was cooled to ambient
temperature, and the trifluoroacetic acid removed in vacua. Trituration of the residue with
diethyl ether (2 x 25 ml) yielded 2-{3-[(6-fluoro-7-hydroxyquinazolrn-4-yl)amino]-lH-
pyrazol-5-yl}-7V-(3-fluorophenyl)acetamide (2.00 g, 100 % yield) as a pale yellow solid :
MS (+ve ESI): 397 (M+H)+.
e) Caesium carbonate (2.67 g, 8.2 mmol) was added to a stirred solution of 2-{3-[(6-
fluoro-7-hydroxyquinazolu>4-yl)amino]-lJY-pyrazol-5-yl}-Ar-(3-fluorophenyl)acetarnide
(2.09 g, 4.10 mmol) and 3-bromo-l-chloropropane (0.44 ml, 4.5 mmol) in
dimethylformamide (20 ml) and the reaction heated at 70 °C for 1 hour. The reaction was

cooled to ambient temperature, poured into water (150 ml) and the resultant solid was collected by suction filtration. Purification by flash chromatography on silica gel, eluting with 3-8% methanol: dichloromethane gave 2-(3-{[7-(3-chloropropoxy)-6-fluoroquinazolin-4~ yl]amino}-l/f-pyrazol-5-yl)-JV"-(3-fluorophenyl)acetamide (1.10 g, 57 % yield) as a pale yellow solid, following solvent evaporation in vacua : MS (+ve ESI): 473 (M+H)+.
f) An analogous reaction to that described in example 45d, but starting with 2-
(ethylamino)ethanol (282 mg, 3.17 mmol) and 2-(3- {[7-(3 -chloropropoxy)-6-
:fluoroquinazoh^-4-yl]amino}-lJ:f-pyrazol-5-yl)-A'-(3-fluorophenyl)acetamide (500 mg, 1.06
mmol) yielded 2-{3-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}-6-fluoroquinazolin-4-
yl)aniino]-ljff-pyrazol-5-yl}-A'-(3-fluorophenyl)acetamide (408 mg, 73 % yield) as an off-
white solid:
'H-NMR (DMSO d6) : 12.40 (s, IH), 10.40 (s, IH), 10.15 (s, IH), 8.53 (s, IH), 8.50 (br s, IH), 7.62 (d, IH), 7.35 (m, 3H), 6.89 (m, IH), 6.78 (br s, IH), 4.28 (m, 3H), 3.75 (br s, 2H), 3.45 (m, 2H), 2.62 (t, 2H), 2.50 (m, 4H under DMSO), 1.91 (m, 2H), 0.98 (t, 3H) : MS (+ve ESI) : 526 (M+H)+.
g) An analogous reaction to that described in example 6c, but starting with 2-{3-[(7-{3-
[ethyl(2-hydroxyemyl)ammo]propoxy}-6-fluoroqumazolm-4-yl)amino]-lJ:f-pyrazol-5-yl}-A'-
(3~fluorophenyl)acetamide (266 mg, 0.51 mmol) yielded di-tert-butyl 2-{ethyl[3-({6-fluoro-
4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoemyl}-lJ^-pyrazol-3-yl)amino]quinazolin-7-
y]}oxy)propyl]amino} ethyl phosphate (288 mg, 79 % yield) as a pale yellow solid :
'H-NMR (CDCW .-12.70 (br s, IH), 9.90 (br s, IH), 9.40 (s, m), 8.60 (s, IH), 7.98 (d, IH),
7.56 (d, IH), 7.15-7.30 (m, 3H), 6.76 (m, IH), 6.24 (br s, IH), 4.14 (t, 2H), 4.03 (q, 2H), 3.83
(s, 2H), 2.79 (t, 2H), 2.70 (t, 2H), 2.61 (m, 2H), 1.95 (m, 2H), 1.48 (s, 18H), 1.05 (t, 3H) :
MS(+veESI):718(M+H)+.
2-(3-amino-ljy-pyrazol-5-yl)-7V-(3-fluorophenyl)acetamide used in step 50c was prepared as
follows:
h) Pentafluorophenyl trifluoroacetate (11.9 g, 42.5 mmol) was added dropwise to a
solution of (3-ammo-l/f-pyrazol-5-yl)acetic acid (3.00 g, 21.3 mmol) and pyridine (3.80 ml,
46.7 mmol) in dimethylformamide (25 ml) at 0 °C. The reaction was allowed to warm to
ambient temperature over 90 minutes before addition of 3-fluoroaniline (4.10 nil, 42.5 niml).
The reaction was stirred for 2.5 hours at ambient temperature and then poured into 0.2 N
hydrochloric acid and extracted with dichloromethane (3 x 50 ml). Addition of excess diethyl

ether caused precipitation of 2,2,2-trifluoro-7V-(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l#-pyrazol-3-yl)acetarnide (2.08 g, 30 % yield) which was isolated as a pale orange solid: MS(-fveESI):331(M+H)+.
i) A solution of 2,2,2-trifluoro-iV-(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} -1H-pyrazol-3-yl)acetamide (3.10 g, 9.4 mmol) in methanol (2.5 ml) and 2.0N aqueous hydrochloric acid (20 ml, 40 mml) was heated at 50 °C for 2.5 hours. The reaction was ' cooled to ambient temperature, basified with solid sodium hydrogen carbonate and then concentrated in vacua until a solid began to precipitate. Collection of the resultant solid by suction filtration followed by prolonged drying in vacua yielded 2-(3-amino-lff-pyrazol-5-^l)-7V-(3-fluorophenyl)acetamide (1.05 g, 48 % yield) as a pale brown solid : H-NMR (DMSO d6): 11.25 (br s, 1H), 10.30 (br s 1H), 7.60 (d, 1H), 7.32 (m, 2H), 6.86 (m, iH), 5.31 (s, 1H), 4.62 (br s, 2H), 3.48 (s, 2H).

CLAIMS
1. A compound of formula (I):
Figure Remove
wherein A is 5-membered heteroaryl containing a nitrogen atom and optionally containing one or two further nitrogen atoms; X is O, S, S(O), S(0)2 or NR14; m is 0, 1, 2 or 3;
Z is a group selected from -NR'R2, phosphonooxy, Ca-ecycloalkyl which Cs-ecycloalkyl is substituted by phosphonooxy or Ci^alkyl substituted by phosphonooxy, and a 4- to 7-membered ring linked via a carbon atom containing a nitrogen atom and optionally containing a further nitrogen atom, which ring may be saturated, partially saturated or unsaturated wherein the ring is substituted on carbon or nitrogen by phosphonooxy or Ci^alkyl substituted by phosphonooxy, and wherein the ring is optionally further substituted on carbon or nitrogen by 1, 2 or 3 halo or Cj^alkyl groups;
R1 is a group selected from-COR8, —CONRSR9 and Ci-galkyl which Cj^alkyl is substituted by phosphonooxy and optionally further substituted by 1 or 2 halo or methoxy groups; R2 is a group selected from hydrogen, -COR10, -CONR10RU and Chalky! which d.6alkyl is optionally substituted by 1, 2 or 3 halo or Q^alkoxy groups or -S(O)pRn (where p is 0, 1 or 2) or phosphonooxy, or R2 is a group selected from Ca-ealkenyl, Ca-ealkynyl, Cj-gcycloalkyl and Ca-ecycloalkylC] ^alkyl;
or R1 and R2 together with the nitrogen to which they are attached form a 4- to 7- membered ring optionally containing a further nitrogen atom which ring may be saturated, unsaturated or partially saturated wherein the ring is substituted on carbon or nitrogen by a group selected from phosphonooxy and Chalky! which Chalky! is substituted by phosphonooxy or -NR8R9, and where the ring is optionally further substituted on carbon or nitrogen by 1,2 or 3 halo or Ci_4alkyl groups;

R3 is a grouop selected from hydrogen, halo, cyano, nitro, Ci-ealkoxy, Ci-ealkyl, -OR12, -
CHR12R13, -OC(O)R12, -C(0)R12, -NR12C(O)R13, -C(O)NR12R13, -NR12SO2R13 and-
NRI2R13;
R4 is hydrogen or a group selected from Ci^alkyl, heteroaryl, heteroarylC] ^alkyl, aryl and
arylCj^alkyl which group is optionally substituted by 1, 2 or 3 substitutents selected from
halo, methyl, ethyl, cyclopropyl and ethynyl;
Rs is selected from hydrogen, Cj^alkyl, C2-4alkenyl, C2^alkynyl, Ca-ecycloalkyl and €3-
R6 and R7 are independently selected from hydrogen, halo, Chalky!, Ca-ecycloalkyl, iydroxy
and Cj^alkoxy;
R8 is Ci-4alkyl substituted by phosphonooxy and optionally further substituted by 1 or2 halo
or methoxy groups;
R9 is selected from hydrogen and Ci^alkyl;
R10 is selected from hydrogen and Ci^alkyl (optionally substituted by halo, CMalkoxy, S(O)q
(where q is 0, 1 or 2) or phosphonoxy);
R11, R12, R13 and R14 are independently selected from hydrogen, Chalky! and heterocjclyl;
or a pharmaceutically acceptable salt thereof.
2. A compound according to claim 1 wherein A is a group of formula (a), (b), (c), jd) or (e):



N
Figure Remove
(a)

(b)

// N '/ V
N
(c)


Figure Remove

** N H

(d) (e)
/here * is the point of attachment to the X group of formula (I) and ** is the point of ttachment to the (CR6R7) group of formula (I); or a pharmaceutically acceptable salt the? of.

3. A compound according to claim 2 wherein A is a group of formula (a) as defined in
claim 2; or a pharmaceutically acceptable salt thereof.
4. A compounds according to any one of claims 1,2 or 3 wherein X is NH; or a
pharmaceutically acceptable salt thereof.
5. A compound according to any one of the preceding claims wherein Z is —NRJR2 or a
5- to 6-membered saturated ring linked via a carbon atom containing a nitrogen atom and
optionally containing a further nitrogen atom, wherein the ring is substituted on carbon or
nitrogen by phosphonooxy or Chalky] substituted by phosphonooxy; or a pharmaceutically
acceptable salt thereof.
6. A compound according to any one of the preceding claims wherein R1 is Chalky!
substituted by phosphonooxy and R2 is a group selected from hydrogen and Cj-galkyl which
Cj-ealkyl is optionally substituted by 1,2 or 3 halo or Cj^alkoxy groups, or R2 is a group
selected from C2-6alkenyl, Ca-ealkynyl, Cs-gcycloalkyl and Cs-ecycloalkylCMalkyl; or a
pharmaceutically acceptable salt thereof.
7. A compound according to any one of the preceding claims wherein R1 is 2-
phosphonooxyethyl; or a pharmaceutically acceptable salt thereof.
8. A compound according to any one of claims 1 to 5 where Z is —ISTR'R2 and R1 and R2
together with the nitrogen to which they are attached form a piperidine, pyrrolidine or
Diperazine ring which is substituted by a group selected from phosphonooxy,
phosphonooxymethyl, 2-phosphonooxyethyl, Af-ethyl-A^2-phosphonooxyethyl)aminomethyl
and JV"-(2-phosphonooxyethyl)aminomethyl and where the ring is optionally further
substituted by 1 or 2 methyl; or a pharmaceutically acceptable salt thereof.
9. A compound according to claim 8 wherein R1 and R2 together with the nitrogen to which they are attached form 2-(phosphonooxymethyl)pyrrolidinyl; or a pharmaceutically acceptable salt thereof.

10. A compound according to any one of the preceding claims wherein R4 is 3-
fluorophenyl, 3,5-difluorophenyl or 2,3-difluorophenyl; or a pharmaceutically acceptable salt
thereof.
11. A compound according to any one of the preceding claims wherein R3 is C\^alkoxy,
halo or hydrogen; or a pharmaceutically acceptable salt thereof.
12. A compound selected from:
{1 .-[3-( {4-[(5- {2-[(3-fluorophenyl)amino]-2-oxoethyl} -lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]piperidin-4-yl}metliyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoemyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate; {(25)-l-[3-({4-[(5-{2-[(3,5-difluorophenyl)amino]-2-oxoethyl}-lJff-pyrazol-3-yl)amino]-6-methoxyquinazolhi-7-yl} oxy)propyI]pyrrolidin-2-yl} methyl dihydrogen phosphate; {(2^)-l-[3-({4-[(5-{2-[(3J5-difluorophenyl)ammo]-2-oxoe%l}-lJf-pyrazol-3-yl)ainino]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; {(26)-l-[3-({4-[(5-{2-[(3-fluorophenyl)arnmo]-2-oxoemyl}-lS'-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l/f-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](propyl)amino] ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)anaino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl] (isobutyl)amino]ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)arnmo]-2-oxoethyl}4fl"-pyrazol-3-yl)aniino]-6-methoxyquinazolin-7-yl} oxy)propyl](isobutyl)amino]ethyl dihydrogen phosphate; 2-[[3
{(2/2)-1-[3-({4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl} -l#-pyrazol-3-yl)ammo]-6-methoxyquinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(3,5-difluorophenyl)amtoo]-2-oxoethyl}4H-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl) oxy)propyl](prop-2-yn-l-yl)amino] ethyl dihydrogen phosphate; 2-[[3-( {4-[(5- {2-[(2,3-difluorophenyl)amino]-2-oxoethyl}- lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](isopropyl)amino]ethyl dihydrogen phosphate; 2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amuio]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl](prop-2-yn-l-yl)amino]ethyl dihydrogen phosphate; 2-[[3 2-{allyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amuio]-2-oxoethyl}-l^-pyrazol-3-yl)aniino]-6-methoxyquinazolin-7-yl} oxy)propyl]amino} ethyl dihydrogen phosphate; 2-{cyclobutyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l//'-pyrazbl-3-yl)amino]-6-methoxyquinazolin-7-yl} oxy)propyl]amino} ethyl dihydrogen phosphate; 2-{cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lJ^-pyrazol-3-yl)amino]-6-rnethoxyquinazolin-7-yl} oxy)propyl]amino} ethyl dihydrogen phosphate; 2-{cyclopropyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l//-pyrazol-3-yl)arnrno]-6-methoxyquinazolin-7-yl} oxy)propyl]amino}ethyl dihydrogen phosphate; 2-{(cydopropyhnethyl)[3-({4-[(5-{2-[(2,3-difliiorophenyl)amino]-2-oxoethyl}-lJ:/-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate; 2-{cyclobutyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino} ethyl dihydrogen phosphate; 2-{4-[({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lJ:f-pyrazol-3-/l)amino]quinazolin-7-yl}oxy)methyl]piperidin-l-yl}ethyl dihydrogen phosphate; 2-[[3_({4-[(5-{2-[(23-difluorophenyl)amino]-2-oxoethyl}-lfl'-pyrazol-3-yl)arnmo]-juinazolin-7-yl}oxy)propyl](ethyl)amino] ethyl dihydrogen phosphate;

2-[[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lF-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)pr.opyl](isopropyl)amino] ethyl dihydrogen phosphate;
3-{[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxpethyl}-lIf-pyrazol-3-
yl)aminoJquinazolin-7-yl}oxy)propyl]amino}-3-methylbutyl dihydrogen phosphate;
2-{(25)-l-[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)ajmino]-
quinazolin-7-yl}oxy)propyl]pyrrolidin-2-yl} ethyl dihydrogen phosphate;
{(2^)-l-[3-({4-[(5-{2-[(253-difluorophenyl)amino]-2-oxoethyl}4^-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(233-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)ammo]-
quinazolin-7-yl}oxy)propyl](propyl)amino]ethyl dihydrogen phosphate;
2-[[3 quinazolin-7-yl}oxy)propyl](biatyl)arnino]ethyl dihydrogen phosphate;
2-{cyclopentyl[3-({4-[(5-{2-[(2,3-difluorophenyl)amino]~2-oxoethyl}-l//'-pyrazol-3-
yl)amino]-quinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate;
{(26)-l quinazolm-7-yl}oxy)propyl]pyrrolidin-2-yl}methyl dihydrogen phosphate;
{(25)-1 -[3 -({4-[(5 - {2 - [(3-fluorophenyl)amino] -2-oxoethyl} -1 H-pyrazol-3 -yl)amino] -
quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl} methyl dihydrogen phosphate;
2-{cyclopentyl[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-l^-pyrazol-3-yl)amino]-
quinazolin-7-yl}oxy)propyl]amino}ethyl dihydrogen phosphate;
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoe1hyl}-lJH-pyrazol-3-yl)arnino]-quinazolin-7-
yl}oxy)propyl](ethyl)amino]ethyl dihydrogen phosphate;
--{[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-17/-pyrazol-3-yl)amino]quniazolin-7-
/!}oxy)propyl]amino} -2-methylpropyl dihydrogen phosphate;
'"[[3-({4-[(5-{2-[(3-fluorophenyl)arnino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-quinazolin-7-
yl}oxy)propyl](propyl)amino] ethyl dihydrogen phosphate;
{(2^)-l-[3-({4-[(5-{2-[(3-fluorophenyl)amino]-2-oxoethyl}-lJff-pyrazol-3-yl)amino]-
quinazolin-7-yl} oxy)propyl]pyrrolidin-2-yl} methyl dihydrogen phosphate;
3-[[3-({4-[(5-{2-[(3-fluorophenyl)ammo]-2-oxoethyl}-l^-pyrazol-3-yl)arnino]-quinazolm-7-
yl}oxy)propyl](ethyl)amino]propyl dihydrogen phosphate
2-[[3-({4-[(5-{2-[(3-fluorophenyl)amiiio]-2-oxoethyl}-ljy-pyrazol-3-yl)aniino]quinazolin-7-
yl}oxy)propyl](2-methoxyethyl)amino]ethyl dihydrogen phosphate

2-[[4-({4-[(5-{2-[(2,3-difluorophenyl)amino]-2-oxoethyl}-lH-pyrazol-3-yl)amino]-quinazolin-7-yl}oxy)butyl](propyl)amino] ethyl dihydrogen phosphate; 2-[[4 13. A pharmaceutical composition comprising a compound according to any one of the
preceding claims in association with a pharmaceutically acceptable diluent or carrier.
14. Use of a compound according to any one of claims 1 to 12 in therapy.
15. Use of a compound according to any one of claims 1 to 12 in the preparation of a
medicament for the treatment of a disease where the inhibition of one or more Aurora kinase
is beneficial.
16. Use according to claim 15 wherein Aurora kinase is Aurora-A kinase or Aurora-B
kinase.
17. Use of a compound according to any one of claims 1 to 12 in the preparation of a
medicament for the treatment of colorectal, breast, lung, prostate, pancreatic or bladder and
renal cancer or leukemias or lymphomas
18. A method of treating a human suffering from a disease in which the inhibition of one
or more Aurora kinases is beneficial, comprising the steps of administering to a person in
need thereof a therapeutically effective amount of a compound as defined in claim 1 or a

pharmaceutically acceptable salt thereof.
19. A method of treating a human suffering from colorectal, breast, lung, prostate,
pancreatic or bladder and renal cancer or leukemias or lymphomas, comprising the steps of
administering to a person in need thereof a therapeutically effective amount of a compound as
deinined in claim 1 or a pharmaceutically acceptable salt thereof.
20. A process for the preparation of a compound of formula (I) as defined in claim 1 or a
pharmaceutically acceptable salt thereof, which process comprises converting a compound of
formula (II) into a compound of formula (I) by phosphorylation of an appropriate hydroxy
group:
Figure Remove

formula (II)
where A, X, m, R3, R4, R5, R6, R7 and R9 are as defined for formula (I); and Z' is a group selected from -NR1 R2, hydroxy, Ca-ecycloalkyl which Cs^cycloalkyl is substituted by hydroxy or Ci^alkyl substituted by hydroxy, and a 4- to 7-membered ring linked via a carbon atom containing a nitrogen atom and optionally containing a further nitrogen atom, which ring may be saturated, unsaturated or partially saturated wherein the ring is substituted on carbon or nitrogen by hydroxy or Chalky! substituted by hydroxy and wherein the ring is optionally further substituted on carbon or nitrogen by 1, 2 or 3 halo or C^alkyl groups; R1 is a group selected from -COR8', -CONR8>R9 and C^alkyl which Ci.6alkyl is substituted by hydroxy
rjy
and optionally further substituted by 1 or 2 halo or methoxy groups; R is a group selected from hydrogen, -COR!0, -CONR'V and C^alkyl which Chalky! is optionally substituted by 1, 2 or 3 halo or Ci^alkoxy groups or-S(0)pRn (where p is 0,1 or 2) or hydroxy, or R2 is a group selected from C2-6alkenyl, C2-6alkynyl, Ca-gcycloalkyl and C3_6cycloalkylCj_4alkyl; or R1 and R2 together with the nitrogen to which they are attached form a 4- to 7- membered ring optionally containing a further nitrogen atom which may be saturated, unsaturated or

partially saturated wherein the ring is substituted on carbon or nitrogen by a group selected
from hydroxy and Chalky! which Ci-4alkyl is substituted by hydroxy or -NR8'R9 and where
the ring is optionally further substituted on carbon or nitrogen by 1,2 or 3 halo or Chalky!
groups; and where R8 is Chalky! substituted by hydroxy and optionally further substituted
by 1 or 2 halo or methoxy groups:
and thereafter if necessary:
i) converting a compound of formula (I) into another compound of formula (I); and/or
ii) removing any protecting groups; and/or
iii) forming a pharmaceutically acceptable salt thereof.

Documents:

2718-DELNP-2005-Abstract (02-11-2007).pdf

2718-delnp-2005-abstract.pdf

2718-DELNP-2005-Claims (02-11-2007).pdf

2718-delnp-2005-claims.pdf

2718-DELNP-2005-Correspondence-Others (01-11-2007).pdf

2718-delnp-2005-correspondence-others.pdf

2718-DELNP-2005-Description (Complete) (02-11-2007).pdf

2718-delnp-2005-description (complete).pdf

2718-DELNP-2005-Form-1 (02-11-2007).pdf

2718-delnp-2005-form-1.pdf

2718-delnp-2005-form-18.pdf

2718-DELNP-2005-Form-2 (02-11-2007).pdf

2718-delnp-2005-form-2.pdf

2718-DELNP-2005-Form-3 (02-11-2007).pdf

2718-delnp-2005-form-3.pdf

2718-delnp-2005-form-5.pdf

2718-DELNP-2005-GPA (02-11-2007).pdf

2718-delnp-2005-gpa.pdf

2718-DELNP-2005-PCT-409 (02-11-2007).pdf

2718-delnp-2005-pct-409.pdf

2718-DELNP-2005-PCT-416 (02-11-2007).pdf

2718-delnp-2005-pct-416.pdf

2718-delnp-2005-pct-notificatian.pdf

2718-delnp-2005-pct-search report.pdf

2718-DELNP-2005-Petition -137 (02-11-2007).pdf

2718-DELNP-2005-Petition -138 (02-11-2007).pdf


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Patent Number 219577
Indian Patent Application Number 2718/DELNP/2005
PG Journal Number 26/2008
Publication Date 27-Jun-2008
Grant Date 08-May-2008
Date of Filing 20-Jun-2005
Name of Patentee ASTRAZENECA AB
Applicant Address
Inventors:
# Inventor's Name Inventor's Address
1 FREDERIC HENRI JUNG
2 INCOLA MURDOCH HERON
3 GEORGES RENE PASQUET
4 ANDREW AUSTEN MORTLOCK
PCT International Classification Number C07F 9/6512
PCT International Application Number PCT/GB2003/005613
PCT International Filing date 2003-12-22
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 03291315.4 2003-06-02 EUROPEAN UNION
2 02293238.8 2002-12-24 EUROPEAN UNION