AU2013201157B2 - Indole derivatives as s1p1 receptor agonists - Google Patents

Abstract

C:\NRPortbl\DCC\FMT\4957806_I.DOC-27/02/20l3 The invention relates to compounds of formula (1) wherein one of R5 and R6 is hydrogen or R2 and the other is (a) processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions or disorders which are mediated via the S1 P1 receptor.

Description

C:\NRPortbl\DCC\FMT\4957186_1.DOC-27/022013 INDOLE DERIVATIVES AS S1 P1 RECEPTOR AGONISTS This is a divisional of Australian Patent Application No. 2007336224, the entire contents of which are incorporated herein by reference. 5 The present invention relates to novel oxadiazole derivatives having pharmacological activity, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of various disorders. 10 Sphingosine 1-phosphate (S1P) is a bioactive lipid mediator formed by the phosphorylation of sphingosine by sphingosine kinases and is found in high levels in the blood. It is produced and secreted by a number of cell types, including those of hematopoietic origin such as platelets and mast cells (Okamoto et al 1998 J Biol Chem 273(42):27104; Sanchez and Hla 2004, J Cell Biochem 92:913). It has a wide range of 15 biological actions, including regulation of cell proliferation, differentiation, motility, vascularisation, and activation of inflammatory cells and platelets (Pyne and Pyne 2000, Biochem J. 349: 385). Five subtypes of S1 P responsive receptor have been described, S1P1 (Edg-1), S1P2 (Edg-5), S1P3 (Edg-3), S1P4 (Edg-6), and S1P5 (Edg-8), forming part of the G-protein coupled endothelial differentiation gene family of receptors (Chun et 20 al 2002 Pharmacological Reviews 54:265, Sanchez and Hla 2004 J Cellular Biochemistry, 92:913). These 5 receptors show differential mRNA expression, with S1 P1-3 being widely expressed, S1 P4 expressed on lymphoid and hematopoietic tissues and S1 P5 primarily in brain and to a lower degree in spleen. They signal via different subsets of G proteins to promote a variety of biological responses (Kluk and Hla 2002 Biochem et Biophysica Acta 25 1582:72, Sanchez and Hla 2004, J Cellular Biochem 92:913). Proposed roles for the S1 P1 receptor include lymphocyte trafficking, cytokine induction/suppression and effects on endothelial cells (Rosen and Goetzl 2005 Nat Rev Immunol. 5:560). Agonists of the S1P1 receptor have been used in a number of 30 autoimmune and transplantation animal models, including Experimental Autoimmune Encephalomelitis (EAE) models of MS, to reduce the severity of the induced disease (Brinkman et al 2003 JBC 277:21453; Fujino et al 2003 J Pharmacol Exp Ther 305:70; Webb et al 2004 J Neuroimmunol 153:108; Rausch et al 2004 J Magn Reson Imaging 20:16). This activity is reported to be mediated by the effect of S1 P1 agonists on 35 lymphocyte circulation through the lymph system. Treatment with S1 P1 agonists results in the sequestration of lymphocytes within secondary lymphoid organs such as the lymph nodes, inducing a reversible peripheral lymphopoenia in animal models (Chiba et al 1998, J Immunology 160:5037, Forrest et al 2004 J WO 2008/074821 PCT/EP2007/064185 Pharmacol Exp Ther 309:758; Sanna et al 2004 JBC 279:13839). Published data on agonists suggests that compound treatment induces loss of the S1P1 receptor from the cell surface via internalisation (Graler and Goetzl 2004 FASEB J 18:551; Matloubian et al 2004 Nature 427:355; Jo et al 2005 Chem Biol 12:703) and it is this 5 reduction of S1 P1 receptor on immune cells which contributes to the reduction of movement of T cells from the lymph nodes back into the blood stream. S1P1 gene deletion causes embryonic lethality. Experiments to examine the role of the S1 P1 receptor in lymphocyte migration and trafficking have included the adoptive 10 transfer of labelled S1P1 deficient T cells into irradiated wild type mice. These cells showed a reduced egress from secondary lymphoid organs (Matloubian et al 2004 Nature 427:355). S1P1 has also been ascribed a role in endothelial cell junction modulation (Allende et 15 al 2003 102:3665, Blood Singelton et al 2005 FASEB J 19:1646). With respect to this endothelial action, S1P1 agonists have been reported to have an effect on isolated lymph nodes which may be contributing to a role in modulating immune disorders. S1P1 agonists caused a closing of the endothelial stromal 'gates' of lymphatic sinuses which drain the lymph nodes and prevent lymphocyte egress (Wei 20 wt al 2005, Nat. Immunology 6:1228). The immunosuppressive compound FTY720 (JP11080026-A) has been shown to reduce circulating lymphocytes in animals and man, have disease modulating activity in animal models of immune disorders and reduce remission rates in relapsing 25 remitting Multiple Sclerosis (Brinkman et al 2002 JBC 277:21453, Mandala et al 2002 Science 296:346, Fujino et al 2003 J Pharmacology and Experimental Therapeutics 305:45658, Brinkman et al 2004 American J Transplantation 4:1019, Webb et al 2004 J Neuroimmunology 153:108, Morris et al 2005 EurJ Immunol 35:3570, Chiba 2005 Pharmacology and Therapeutics 108:308, Kahan et al 2003, Transplantation 30 76:1079, Kappos et al 2006 New Eng J Medicine 335:1124). This compound is a prodrug that is phosphorylated in vivo by sphingosine kinases to give a molecule that has agonist activity at the S1P1, S1P3, S1P4 and S1P5 receptors. Clinical studies have demonstrated that treatment with FTY720 results in bradycardia in the first 24 hours of treatment (Kappos et al 2006 New Eng J Medicine 335:1124). The 35 bradycardia is thought to be due to agonism at the S1P3 receptor, based on a number of cell based and animal experiments. These include the use of S1 P3 knock 2 WO 2008/074821 PCT/EP2007/064185 out animals which, unlike wild type mice, do not demonstrate bradycardia following FTY720 administration and the use of S1 P1 selective compounds. (Hale et al 2004 Bioorganic & Medicinal Chemistry Letters 14:3501, Sanna et al 2004 JBC 279:13839, Koyrakh et al 2005 American J Transplantation 5:529) 5 Hence, there is a need for S1 P1 receptor agonist compounds with selectivity over S1 P3 which might be expected to show a reduced tendency to induce bradycardia. The following patent applications describe oxadiazole derivatives as S1 P1 agonists: 10 W003/105771, W005/058848, W006/047195, W006/100633, W006/115188, W006/131336, W007/024922 and W007/116866. The following patent application describes indole-oxadiazole derivatives as antipicornaviral agents: W096/009822. The following patent applications describe 15 indole-carboxylic acid derivatives as leukotriene receptor antagonists, pesticides and agrochemical fungicides respectively: W006/090817, EP 0 439 785 and DE 39 39 238. A structurally novel class of compounds has now been found which provides 20 agonists of the S1P1 receptor. The present invention therefore provides compounds of formula (1) or a pharmaceutically acceptable salt thereof thereof: R5 R6 Ry

R

5 N O R2 Z4 OH(J 25 wherein one of R 5 and R 6 is hydrogen or R 2 and the other is (a) N R 1i (a) A is a phenyl or a 5 or 6-membered heteroaryl ring; 3 WO 2008/074821 PCT/EP2007/064185

R

1 is hydrogen or up to three substituents independently selected from halogen, C(1. 6 )alkyl, C( 3

-

6 )cycloalkyl, C( 1

.

6 )alkoxy, C( 3

-

6 )cycloalkyloxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl, cyano, nitro, optionally substituted piperidine, optionally substituted pyrrolidine, optionally substituted phenyl and optionally 5 substituted 5 or 6 membered heteroaryl rings; when R 1 is phenyl, piperidine, pyrrolidine or a 5 or 6 membered heteroaryl ring it may be substituted by up to three substituents selected from halogen, C( 1

.

6 )alkyl, C(1. 6 )alkoxy, trifluoromethoxy, difluoromethoxy, C 3

-

6 cycloalkyl, trifluoromethyl and cyano;

R

2 is hydrogen or up to three substituents independently selected from halogen, C(1. 10 4 )alkyl, C( 1

.

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl and cyano;

R

7 is hydrogen or halogen; Z is C( 1

.

4 )alkyl which is optionally interrupted by N or 0 and is optionally substituted by halogen or methyl. 15 In one embodiment, when A is phenyl or pyridyl R 1 is two substituents at the para and meta positions on A relative to the oxadiazole ring. In one embodiment, when A is thienyl R 1 is two substiuents at the 4- and 5 positions. 20 In one embodiment of the invention,

R

5 is hydrogen and R 6 is (a); and/or A is thienyl, pyridyl or phenyl; and/or

R

1 is up to three substituents selected from halogen, C 1

.

6 alkoxy, or trifluoromethyl, 25 optionally substituted phenyl, optionally substituted cyclohexyl, cyano, triflouromethoxy, optionally substituted piperidine, optionally substituted pyrrolidine,

C

1

.

6 alkyl and NO 2 ; and/or

R

2 is hydrogen; and/or

R

7 is hydrogen or halogen; and/or 30 Z is C( 1

.

4 )alkyl which is optionally interrupted by N or 0 and is optionally substituted by fluoro or methyl. In one embodiment of the invention,

R

5 is hydrogen and R 6 is (a); and/or 35 A is pyridyl or phenyl; and/or 4 WO 2008/074821 PCT/EP2007/064185

R

1 is up to two substituents selected from halogen, C 1

.

6 alkoxy, or trifluoromethyl, optionally substituted phenyl, optionally substituted cyclohexyl, cyano, triflouromethoxy, optionally substituted piperidine, optionally substituted pyrrolidine,

C

1

.

6 alkyl and NO 2 ; and/or 5 R 2 is hydrogen; and/or

R

7 is hydrogen, chloro or bromo; and/or Z is unsubstituted C( 2

-

3 )alkyl. In one embodiment of the invention, 10 R 5 is hydrogen and R 6 is (a); and/or A is pyridyl or phenyl; and/or

R

1 is up to two substituents selected from chloro, bromo, methoxy, propoxy, isopropoxy, trifluoromethyl, halo substuituted phenyl, phenyl, cyclohexyl, cyano, triflouromethoxy, piperidine, pyrrolidine, ethyl or NO 2 .; and/or 15 R 2 is hydrogen; and/or

R

7 is hydrogen, chloro or bromo; and/or Z is unsubstituted C( 2

-

3 )alkyl. In one embodiment of the invention, 20 R 5 is hydrogen and R 6 is (a); and/or A is pyridyl or phenyl; and/or

R

1 is up to two substituents selected from chloro, isopropoxy and cyano; and/or

R

2 is hydrogen; and/or

R

7 is hydrogen; and/or 25 Z is unsubstituted C( 2

-

3 )alkyl. In one embodiment of the invention,

R

5 is (a) and R 6 is hydrogen. A is optionally substituted thiophene or phenyl; and/or 30 R 1 is hydrogen, halogen, C 14 alkoxy, or trifluoromethyl; and/or

R

2 is hydrogen; and/or Z is ethylene. In another embodiment of the invention, 35 R 5 is (a) and R 6 is hydrogen; and/or A is thiophene substituted by phenyl; and/or 5 WO 2008/074821 PCT/EP2007/064185

R

1 is hydrogen, halogen, C 14 alkoxy, or trifluoromethyl; and/or

R

2 is hydrogen; and/or Z is ethylene. 5 When R 1 is phenyl or a 5 or 6 membered heteroaryl ring it may be substituted by up to three substituents selected from halogen, C(1.

4 )alkyl, C( 1

.

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl and cyano. The present invention therefore also provides compounds of formula (IA) or a 10 pharmaceutically acceptable salt thereof: R 6 R R7 3' R0 N X R m i n O H (IA) wherein: 15 one of R 5 and R 6 is hydrogen or R 2 and the other is (a) N R 1 (a) A is a phenyl or a 5 or 6-membered heteroaryl ring; 20 R 1 is hydrogen or up to three substituents independently selected from halogen, C(1. 4 )alkyl, C( 1

.

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl, cyano, optionally substituted phenyl and optionally substituted 5 or 6 membered heteroaryl rings;

R

2 is hydrogen or up to three substituents independently selected from halogen, C(1. 25 4 )alkyl, C( 1

.

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl and cyano;

R

3 , R 3 ,, R 4 and R 4 , are each independently selected from hydrogen, halogen and methyl;

R

7 is hydrogen or halogen; 6 CNRPorbl\DCC\RBR\4745014_1.DOC-15111/2012 X is NH optionally substituted by methyl, 0, CH 2 optionally substituted by fluoro or methyl, or a direct bond; m is 0-2; and n is 0-4. 5 When R 1 is phenyl or a 5 or 6 membered heteroaryl ring it may be substituted by up to three substituents selected from halogen, C(l.

4 )alkyl, C( 1

.

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl and cyano. 10 When X is NH it may be substituted by methyl. When X is CH 2 it may be substituted by fluoro or methyl. In one embodiment of the invention, A is optionally substituted thiophene or phenyl; 15 R 1 is hydrogen, halogen, C1.

4 alkoxy, or trifluoromethyl;

R

2 , R 3 and R 4 are each hydrogen; X is a direct bond; m is 2; and n is 0. 20 In another embodiment of the invention, A is thiophene substituted by phenyl;

R

1 is hydrogen, halogen, C 1

.

4 alkoxy, or trifluoromethyl;

R

2 , R 3 and R 4 are each hydrogen; 25 X is a direct bond; m is 2; and n is 0 In another embodiment, the present invention provides a compound of formula (IA) or a 30 pharmaceutically acceptable derivative thereof: R 6 R

R

5 RN X O (A) 7 H:\rec\Intrwovn\NRPortbl\DCC\REC\7438572_I.docx-19/03/2015 wherein one of R 5 and R 6 is hydrogen or R 2 and the other is (a) OAN N R 1 (a) A is a phenyl or a 5 or 6-membered heteroaryl ring;

R

1 is hydrogen or up to three substituents independently selected from halogen, C( 1

_

4 )alkyl,

C(

1

_

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl, cyano, and optionally substituted phenyl or optionally substituted 5 or 6 membered heteroaryl rings;

R

2 is hydrogen or up to three substituents independently selected from halogen, C( 1

_

4 )alkyl,

C(

1

_

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl and cyano;

R

3 , R 3 , R 4 and R 4 , are each independently selected from hydrogen, halogen and methyl;

R

7 is hydrogen or halogen; X is a direct bond; m is 0-2; n is 0-4; and when R 1 comprises a substituted phenyl or 5 or 6 membered heteroaryl ring, it is substituted by up to three substituents independently selected from halogen, C( 1

_

4 )alkyl,

C(

1

.

4 )alkoxy, trifluoromethoxy, difluoromethoxy, trifluoromethyl and cyano. In one aspect, the present invention provides a compound of C1 0 CH 3

CH

3 N N 0 N HO -7A - H:\rec\ntr ovn\NRPortbl\DCC\REC\7438572_I.docx-19/03/2015 4-[4-(5-{5-chloro-6-[(1 -methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]butanoic acid and pharmaceutically acceptable salts thereof. In another aspect, the present invention provides use of a compound as herein defined in the manufacture a medicament for use in the treatment of conditions or disorders mediated by S1 P1 receptors, wherein the condition or disorder is multiple sclerosis, autoimmune disease, chronic inflammatory disorder, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, ulcerative colitis, lupus erythematosis, psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular disease, pain conditions, acute viral disease, inflammatory bowel conditions, insulin and non-insulin dependent diabetes. In another aspect, the present invention provides a method for the treatment of conditions or disorders mediated by S1 P1 receptors comprising administering to the sufferer a therapeutically effective amount of a compound as herein defined, wherein the condition or disorder is multiple sclerosis, autoimmune disease, chronic inflammatory disorder, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, ulcerative colitis, lupus erythematosis, psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular disease, pain conditions, acute viral disease, inflammatory bowel conditions, insulin and non-insulin dependent diabetes. The term "alkyl" as a group or part of a group e.g. alkoxy or hydroxyalkyl refers to a straight or branched alkyl group in all isomeric forms. The term "C(1_6) alkyl" refers to an alkyl group, as defined above, containing at least 1, and at most 6 carbon atoms Examples of such alkyl groups include methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, or tert-butyl. Examples of such alkoxy groups include methoxy, ethoxy, propoxy, iso-propoxy, butoxy, iso-butoxy, sec-butoxy and tert-butoxy. - 7B - WO 2008/074821 PCT/EP2007/064185 Suitable C( 3

-

6 )cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Suitable C( 3

-

6 )cycloalkyloxy groups include cyclopropoxy, cyclobutoxy, cyclopentoxy 5 and cyclohexyloxy. As used herein, the term "halogen" refers to fluorine (F), chlorine (CI), bromine (Br), or iodine (1) and the term "halo" refers to the halogen: fluoro (-F), chloro (-CI), bromo(-Br) and iodo(-1). 10 The term "heteroaryl" represents an unsaturated ring which comprises one or more heteroatoms. When the term heteroaryl represents a 5 membered group it contains a heteroatom selected from 0, N or S and may optionally contain a further 1 to 3 nitrogen atoms. When heteroaryl represents a 6-membered group it contains from 1 15 to 3 nitrogen atoms. Examples of such 5 or 6 membered heteroaryl rings include pyrrolyl, triazolyl, thiadiazolyl, tetrazolyl, imidazolyl, pyrazolyl, isothiazolyl, thiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, furazanyl, furanyl, thienyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl and triazinyl. 20 In certain of the compounds of formula (1), dependent upon the nature of the substituent there are chiral carbon atoms and therefore compounds of formula (1) may exist as stereoisomers. The invention extends to all optical isomers such as stereoisomeric forms of the compounds of formula (1) including enantiomers, diastereoisomers and mixtures thereof, such as racemates. The different 25 stereoisomeric forms may be separated or resolved one from the other by conventional methods or any given isomer may be obtained by conventional stereoselective or asymmetric syntheses. Certain of the compounds herein can exist in various tautomeric forms and it is to be 30 understood that the invention encompasses all such tautomeric forms. Suitable compounds of the invention are: 3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 35 yl)propanoic acid 8 WO 2008/074821 PCT/EP2007/064185 3-[5-(5-{3-Chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol- 1 yl]propanoic acid 3-[3-Chloro-5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H 5 indol-1-yl]propanoic acid 3-(3-Chloro-5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H indol-1-yl)propanoic acid 10 3-(4-{5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1 yl)propanoic acid 3-[4-(5-{3-Chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]propanoic acid 15 3-[4-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 yl]propanoic acid 3-[4-(5-{5-Chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 20 yl]propanoic acid 3-[5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1-yl] propanoic acid 25 (5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1-yl)acetic acid 3-[3-bromo-5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H indol-1-yl]propanoic acid 30 5-[5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]pentanoic acid 4-[5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 35 yl]butanoic acid 9 WO 2008/074821 PCT/EP2007/064185 4-[5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]butanoic acid (2S)-3-[5-(5-{3-ch Ioro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)- 1 H-indol-1 5 yl]-2-methylpropanoic acid 2,2-dimethyl-3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H indol-1-yl)propanoic acid 10 3-[5-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1-yl] 2,2,3-trifluoropropanoic acid 4-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 yl]butanoic acid 15 3-[5-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 yl]propanoic acid 3-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 20 yl]propanoic acid 3-(4-{5-[2-(trifluoromethyl)-4-biphenylyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1-yl)propano ic acid 25 3-(4-{5-[4-cyclohexyl-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1 yl)propanoic acid 3-(4-{5-[4-[(1 -methylethyl)oxy]-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}- 1 H indol-1-yl)propanoic acid 30 [4-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]acetic acid [4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 35 yl]acetic acid 10 WO 2008/074821 PCT/EP2007/064185 3-(4-{5-[2'-fluoro-2-(trifluoromethyl)-4-biphenylyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoic acid 4-[4-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 5 yl]butanoic acid 4-[4-(5-{3-chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]butanoic acid 10 4-[4-(5-{5-chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]butanoic acid 4-(4-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)butanoic acid 15 4-(4-{5-[2-(trifluoromethyl)-4-biphenylyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1-y)butanoic acid 3-(4-{5-[4-(methyloxy)-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 20 yl)propanoic acid 4-{4-[5-(3-cyano-4-{[(1 R)-1 -methylpropyl]oxy}phenyl)- 1,2,4-oxadiazol-3-yl]- 1 H-indol 1-yl}butanoic acid 25 4-{4-[5-(3-cyano-4-{[(1 S)- 1 -methylpropyl]oxy}phenyl)-1,2,4-oxad iazol-3-yl]-1 H-indol 1-yl}butanoic acid 3-(4-{5-[3-ethyl-4-(1-piperidinyl)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1-yl)propanoic acid 30 3-{4-[5-(4-cyclohexyl-3-ethylphenyl)-1,2,4-oxadiazol-3-yl]-1 H-indol-1-yl}propanoic acid 3-(4-{5-[5-chloro-6-(1-pyrrolidinyl)-3-pyridinyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 35 yl)propanoic acid 4-[4-(5-{3-bromo-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]butanoic acid 40 4-(4-{5-[3-ch loro-4-(2-methylpropyl)phenyl]-1,2,4-oxadiazol-3-yl}- 1 H-indol-1 yl)butanoic acid 11 WO 2008/074821 PCT/EP2007/064185 3-(4-{5-[4-(2-methylpropyl)-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol 1-yl)propanoic acid 5 4-(4-{5-[3-cyano-4-(2-methylpropyl)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)butanoic acid 4-{4-[5-(2-cyano-4-biphenylyl)-1,2,4-oxadiazol-3-yl]-1 H-indol-1 -yl}butanoic acid 10 3-(3-Chloro-4-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H indol-1-yl)propanoic acid 3-[3-chloro-5-(5-{3-chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H indol-1-yl]propanoic acid 15 3-(3-chloro-5-{5-[3-chloro-4-(propyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoic acid 3-(3-chloro-5-{5-[3-chloro-4-(methyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 20 yl)propanoic acid 3-(3-chloro-5-{5-[4-(methyloxy)-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-1 H indol-1-yl)propanoic acid 25 3-(3-chloro-5-{5-[3-chloro-4-(ethyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoic acid 3-[3-ch Ioro-5-(5-{3-cyano-4-[(1 -methylethyl)oxy]phenyl}- 1,2,4-oxad iazol-3-yl)- 1 H indol-1-yl]propanoic acid 30 3-(3-chloro-5-{5-[4-nitro-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoic acid 3-[3-chloro-5-(5-{4-chloro-3-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H 35 indol-1-yl]propanoic acid 3-(3-chloro-5-{5-[6-(methyloxy)-3-biphenylyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1 yl)propanoic acid 12 WO 2008/074821 PCT/EP2007/064185 3-(5-{5-[6-(trifluoromethyl)-3-biphenylyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1-yl)propanoic acid 5 3-{5-[5-(4-phenyl-2-thienyl)-1,2,4-oxadiazol-3-yl]-1H-indol-1-yl}propanoic acid 3-{3-chloro-5-[5-(4-cyclohexylphenyl)-1,2,4-oxadiazol-3-yl]-1 H-indol-1 -yl}propanoic acid 10 3-(3-chloro-5-{5-[6-(4-fluorophenyl)-3-pyridinyl]-1,2,4-oxadiazol-3-yl}-1 H-indol- 1 yl)propanoic acid 3-(3-chloro-5-{5-[6-(4-fluorophenyl)-3-pyridinyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1 yl)propanoic acid 15 or pharmaceutically acceptable salts thereof. Pharmaceutically acceptable derivatives of compounds of formula (1) include any pharmaceutically acceptable salt, ester or salt of such ester of a compound of 20 formula (1) which, upon administration to the recipient is capable of providing (directly or indirectly) a compound of formula (1) or an active metabolic or residue thereof. The compounds of formula (1) can form salts. It will be appreciated that for use in medicine the salts of the compounds of formula (1) should be pharmaceutically 25 acceptable. Suitable pharmaceutically acceptable salts will be apparent to those skilled in the art and include those described in J. Pharm. Sci., 1977, 66, 1-19, such as acid addition salts formed with inorganic acids e.g. hydrochloric, hydrobromic, sulfuric, nitric or phosphoric acid; and organic acids e.g. succinic, maleic, acetic, fumaric, citric, tartaric, benzoic, p-toluenesulfonic, methanesulfonic or 30 naphthalenesulfonic acid. Certain of the compounds of formula (1) may form acid addition salts with one or more equivalents of the acid. The present invention includes within its scope all possible stoichiometric and non-stoichiometric forms. Salts may also be prepared from pharmaceutically acceptable bases including inorganic bases and organic bases. Salts derived from inorganic bases include 35 aluminum, ammonium, calcium, copper, ferric, ferrous, lithium, magnesium, manganic salts, manganous, potassium, sodium, zinc, and the like. Salts derived 13 WO 2008/074821 PCT/EP2007/064185 from pharmaceutically acceptable organic bases include salts of primary, secondary, and tertiary amines; substituted amines including naturally occurring substituted amines; and cyclic amines. Particular pharmaceutically acceptable organic bases include arginine, betaine, caffeine, choline, N,N'-dibenzylethylenediamine, 5 diethylamine, 2-diethylaminoethanol, 2-dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethyl-morpholine, N-ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, isopropylamine, lysine, methylglucamine, morpholine, piperazine, piperidine, procaine, purines, theobromine, triethylamine, trimethylamine, tripropylamine, tris(hydroxymethyl)aminomethane (TRIS, trometamol) and the like. 10 Salts may also be formed from basic ion exchange resins, for example polyamine resins. When the compound of the present invention is basic, salts may be prepared from pharmaceutically acceptable acids, including inorganic and organic acids. Such acids include acetic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethanesulfonic, ethanedisulfonic, fumaric, gluconic, glutamic, hydrobromic, 15 hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, pamoic, pantothenic, phosphoric, propionic, succinic, sulfuric, tartaric, p toluenesulfonic acid, and the like. The compounds of formula (1) may be prepared in crystalline or non-crystalline form, 20 and, if crystalline, may optionally be hydrated or solvated. This invention includes within its scope stoichiometric hydrates or solvates as well as compounds containing variable amounts of water and/or solvent. Included within the scope of the invention are all salts, solvates, hydrates, 25 complexes, polymorphs, prodrugs, radiolabelled derivatives, stereoisomers and optical isomers of the compounds of formula (1). In a further aspect, this invention provides processes for the preparation of a compound of formula (1). In one aspect the compound of formula (1) can be prepared 30 by the process in Scheme I where A, Z, R 1 , R 2 , R 7 are as defined for formula (1).. 14 WO 2008/074821 PCT/EP2007/064185 R7

NH

2 OH.HCI HOsN Ry EDCI.HCI, NC - NaHCO 3 | HOBT, DMF NH H2N NH 0 R2 MeGH 2 \l /O MeOH R2 R2 ||| A O CsRO IV O N R7Cs2CO3, i I DMIF A __1 0 N NH 0 RBr~ V2 z VI A N R, aq. NaOH NV N MeGH \\ / VII R2 O'N R7 A I N N OH R2 Scheme I The first step of the process (Il to Ill) is carried out in a suitable solvent, such as methanol or ethanol and is heated to a temperature such at 50-80 OC. In the second 5 step of the process (Ill to V) suitable reagents include EDC.HCI and HOBt in a solvent such as DMF at a temperature between room temperature and 90 OC or alternatively PyBOP in DMF. Alternatively (Ill) may be converted to (V) by treatment with the carboxylic ester of (IV) and sodium ethoxide in ethanol in a microwave reaction at a temperature such as 120 OC. In the third step (V to VII) a base such as 10 cesium carbonate or alternatively potassium carbonate is used and the reaction may be heated either conventionally or using a microwave reactor to a temperature such as 140 OC. The fourth step of the process (VII to I) is carried out in a suitable solvent 15 WO 2008/074821 PCT/EP2007/064185 such as methanol or alternatively ethanol and may be carried out at either room temperature or elevated temperature such as 40 or 50 'C. Compounds of formula (IV) are either commercially available, may be prepared by using methods described in the literature or can be prepared as described in the 5 experimental section. Bromides of formula (VI) are either commercially available or may be prepared by using methods described in the literature or using the methods disclosed. In another aspect the preparation of a compound of formula (1) can be prepared by 10 the process in Scheme II where A, Z, R 1 , R 2 , R 7 are as defined for formula (1). In the first step the reaction (Il to VIII) can be heated to 80 'C. The second step of the process (VIII to IX) is carried out in a suitable solvent such as ethanol or methanol. The third step of this process (IX to VII) requires amide coupling reagents such as EDC.HCI and HOBt in a solvent such as DMF at a temperature between room 15 temperature and 120 'C. The fourth step of the process is carried out in a suitable solvent such as ethanol or methanol. Compounds of formula (IV) are either commercially available, may be prepared by using methods described in the literature or can be prepared as described in the experimental section. Bromides of formula VI are either commercially available or may be prepared by using methods 20 described in the literature or by the methods disclosed. 25 30 35 16 WO 2008/074821 PCT/EP2007/064185 Scheme II 7 CS2CO 3 , R7 NC - NH DMF NC _ NH 2 OH.HCI NZ NaHCO 3 Br~ O R2 Z k d 2 solvent VI VIII HOs R N 7 NR 0 Reagents 7

H

2 N N A Z O N V N 0 R Z R2 O-X

R

2

R

1 IV VII NaOH(aq) O'N R7 solvent , A -0 R N N Z 1i OH R2 5 In cases where the substituent R 7 in formula I is a chlorine atom attached to C-3 of the indole ring this may be introduced in a number of ways. Intermediate (V) in scheme I where R 7 = H and R 1 , R 2 and A are defined as in formula (I) may be treated with N-chlorosuccinimide in dichloromethane to generate the 3-chloro-compound 10 (Va) which can then be converted to (I) as described in scheme I (Scheme III) 17 WO 2008/074821 PCT/EP2007/064185 Scheme Ill Cl A _ NCSA A -1N W AN N NH DCM NH R2 R2 V Va 5 Alternatively, the intermediate (II) where R 7 = H may be chlorinated by treatment with N-chlorosuccinimide in DMF to generate a 3-chloro-indole (Ila) which can be converted to a compound of structure (1) as described in scheme II (Scheme IV). Scheme IV 10 Cl NC - NCS NC NH DCM NH R2 R2 || lla Where R 7 = Br the intermediate (V) where R 7 = H and A, R 1 and R 2 are as defined in formula (1) may be brominated by treatment with Br 2 in DMF to generate (Vb) where Rr = Br (Scheme V). 15 Scheme V Br A A N N N NH I NH Br 2 R R2 R2 V Vb 18 WO 2008/074821 PCT/EP2007/064185 In cases where R 1 is a phenyl group it is possible to introduce this group by a cross coupling reaction on a compound of structure VII to generate Vila (Scheme VI) where A, Z, R 2 and R 7 are as defined in formula (1), and Ar is optionally substituted phenyl, followed by hydrolysis to compound I. In this transformation, M is a group 5 such as B(OH) 2 which allows the cross-coupling reaction to occur, Y is a group such as bromine, iodine or trifluoromethanesulfonate and the catalyst a palladium species such as tetrakistriphenylphosphine palladium(O). Such reactions are typically carried out at elevated temperature. Scheme VI 10 O'N R 7 O'N R7 A - o Ar-M Y NV N" Z_ N ON Y Z catalyst Ar NN J Z VIl Vila In cases where R 1 is an alkoxy group such as O-ethyl or 0-isopropyl the alkyl substituent can be introduced into a compound of formula VII where R 1 = OH and A, 15 Z, R 7 and R 2 are as defined in formula (1) to generate a compound of formula Vllb where R 1 = O-alkyl (Scheme VII). In this case Y is a halogen such as iodine. The reaction may be performed in a polar solvent such as DMF in the presence of a base such as potassium carbonate. 20 Scheme VII ZV D Alkyl-Y N0 VII VIIb In certain cases it is possible to alkylate the intermediate indole (V) where R 1 , R 2 , R 7 25 and A are as defined in formula (1) directly with carboxylic acid-substituted alkyl bromide to generate the final compound (1) without the need for a hydrolysis step (Scheme VIII). A suitable base for this transformation is cesium carbonate. 19 WO 2008/074821 PCT/EP2007/064185 Scheme VIII OR base, O'N R A __1N7DMVF -0 (A \I V N NH D N N RBrN R Z OH V R2 Z OH R2 VI 5 Pharmaceutically acceptable salts may be prepared conventionally by reaction with the appropriate acid or acid derivative. The potencies and efficacies of the compounds of this invention for the S1P1 receptor can be determined by GTPyS assay performed on the human cloned 10 receptor as described herein or by the yeast binding assay, also described herein Compounds of formula (1) have demonstrated agonist activity at the S1 P1 receptor, using functional assays described herein. Compounds of formula (1) and their pharmaceutically acceptable salts are therefore 15 of use in the treatment of conditions or disorders which are mediated via the S1P1 receptor. In particular the compounds of formula (1) and their pharmaceutically acceptable salts are of use in the treatment of multiple sclerosis, autoimmune diseases, chronic inflammatory disorders, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, ulcerative colitis, lupus erythematosis, 20 psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular diseases, pain conditions, acute viral diseases, inflammatory bowel conditions, insulin and non-insulin dependant diabetes (herein after referred to as the "Disorders of the Invention"). 25 It is to be understood that "treatment" as used herein includes prophylaxis as well as alleviation of established symptoms. Thus the invention also provides a compound of formula (1) or a pharmaceutically acceptable salt thereof, for use as a therapeutic substance, in particular in the 30 treatment of the conditions or disorders mediated via the S1 P1 receptor. In particular the invention provides a compound of formula (1) or a pharmaceutically acceptable salt thereof for use as a therapeutic substance in the treatment of multiple sclerosis, 20 WO 2008/074821 PCT/EP2007/064185 autoimmune diseases, chronic inflammatory disorders, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, ulcerative colitis, lupus erythematosis, psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular diseases, pain 5 conditions, acute viral diseases, inflammatory bowel conditions, insulin and non insulin dependant diabetes. The invention further provides a method of treatment of conditions or disorders in mammals including humans which can be mediated via the S1P1 receptor, which comprises administering to the sufferer a therapeutically safe and effective amount of a compound of formula (1) or a pharmaceutically acceptable 10 salt thereof. In another aspect, the invention provides for the use of a compound of formula (1) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in the treatment of the conditions or disorders mediated via the S1 P1 receptor 15 In order to use the compounds of formula (1) and pharmaceutically acceptable salts thereof in therapy, they will normally be formulated into a pharmaceutical composition in accordance with standard pharmaceutical practice. The present invention also provides a pharmaceutical composition, which comprises a compound 20 of formula (1) or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient. In a further aspect, the present invention provides a process for preparing a pharmaceutical composition, the process comprising mixing a compound of formula 25 (1) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient. A pharmaceutical composition of the invention, which may be prepared by admixture, suitably at ambient temperature and atmospheric pressure, is usually adapted for 30 oral, parenteral or rectal administration and, as such, may be in the form of tablets, capsules, oral liquid preparations, powders, granules, lozenges, reconstitutable powders, injectable or infusible solutions or suspensions or suppositories. Orally administrable compositions are generally preferred. 35 Tablets and capsules for oral administration may be in unit dose form, and may contain conventional excipients, such as binding agents (e.g. pregelatinised maize 21 WO 2008/074821 PCT/EP2007/064185 starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate); tabletting lubricants (e.g. magnesium stearate, talc or silica); disintegrants (e.g. potato starch or sodium starch glycollate); and acceptable wetting agents (e.g. sodium lauryl sulphate). The tablets 5 may be coated according to methods well known in normal pharmaceutical practice. Oral liquid preparations may be in the form of, for example, aqueous or oily suspension, solutions, emulsions, syrups or elixirs, or may be in the form of a dry product for reconstitution with water or other suitable vehicle before use. Such liquid 10 preparations may contain conventional additives such as suspending agents (e.g. sorbitol syrup, cellulose derivatives or hydrogenated edible fats), emulsifying agents (e.g. lecithin or acacia), non-aqueous vehicles (which may include edible oils e.g. almond oil, oily esters, ethyl alcohol or fractionated vegetable oils), preservatives (e.g. methyl or propyl-p-hydroxybenzoates or sorbic acid), and, if desired, 15 conventional flavourings or colorants, buffer salts and sweetening agents as appropriate. Preparations for oral administration may be suitably formulated to give controlled release of the active compound. For parenteral administration, fluid unit dosage forms are prepared utilising a 20 compound of the invention or pharmaceutically acceptable salts thereof and a sterile vehicle. Formulations for injection may be presented in unit dosage form e.g. in ampoules or in multi-dose, utilising a compound of the invention or pharmaceutically acceptable derivatives thereof and a sterile vehicle, optionally with an added preservative. The compositions may take such forms as suspensions, solutions or 25 emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen free water, before use. The compound, depending on the vehicle and concentration used, can be either suspended or dissolved in the vehicle. In preparing solutions, 30 the compound can be dissolved for injection and filter sterilised before filling into a suitable vial or ampoule and sealing. Advantageously, adjuvants such as a local anaesthetic, preservatives and buffering agents are dissolved in the vehicle. To enhance the stability, the composition can be frozen after filling into the vial and the water removed under vacuum. Parenteral suspensions are prepared in substantially 35 the same manner, except that the compound is suspended in the vehicle instead of being dissolved, and sterilisation cannot be accomplished by filtration. The 22 WO 2008/074821 PCT/EP2007/064185 compound can be sterilised by exposure to ethylene oxide before suspension in a sterile vehicle. Advantageously, a surfactant or wetting agent is included in the composition to facilitate uniform distribution of the compound. 5 Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilising agents, dispersing agents, suspending agents, thickening agents, or colouring agents. Drops may be formulated with an aqueous or non-aqueous base also comprising one or more dispersing agents, stabilising agents, solubilising agents or suspending agents. They may also 10 contain a preservative. The compounds of formula (1) or pharmaceutically acceptable salts thereof may also be formulated in rectal compositions such as suppositories or retention enemas, e.g. containing conventional suppository bases such as cocoa butter or other glycerides. 15 The compounds of formula (1) or pharmaceutically acceptable salts thereof may also be formulated as depot preparations. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the compounds of the invention may be 20 formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt. For intranasal administration, the compounds of formula (1) or pharmaceutically 25 acceptable salts thereof, may be formulated as solutions for administration via a suitable metered or unitary dose device or alternatively as a powder mix with a suitable carrier for administration using a suitable delivery device. Thus compounds of formula (1) or pharmaceutically acceptable salts thereof may be formulated for oral, buccal, parenteral, topical (including ophthalmic and nasal), depot or rectal 30 administration or in a form suitable for administration by inhalation or insufflation (either through the mouth or nose). The compounds of formula (1) or pharmaceutically acceptable salts thereof may be formulated for topical administration in the form of ointments, creams, gels, lotions, 35 pessaries, aerosols or drops (e.g. eye, ear or nose drops). Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of 23 WO 2008/074821 PCT/EP2007/064185 suitable thickening and/or gelling agents. Ointments for administration to the eye may be manufactured in a sterile manner using sterilised components. The composition may contain from 0.1% to 99% by weight, preferably from 10 to 5 60% by weight, of the active material, depending on the method of administration. The dose of the compound used in the treatment of the aforementioned disorders will vary in the usual way with the seriousness of the disorders, the weight of the sufferer, and other similar factors. However, as a general guide suitable unit doses may be 0.05 to 1000 mg, 1.0 to 500mg or 1.0 to 200 mg and such unit doses may be 10 administered more than once a day, for example two or three times a day. Compounds of formula (1) or pharmaceutically acceptable salts thereof may be used in combination preparations. For example, the compounds of the invention may be used in combination with cyclosporin A, methotrexate, steriods, rapamycin, 15 proinflammatory cytokine inhibitors, immunomodulators including biologicals or other therapeutically active compounds. The subject invention also includes isotopically-labeled compounds, which are identical to those recited in formulas I and following, but for the fact that one or more 20 atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, iodine, and chlorine, such as 3 H, 11C, 14C, 1 8 F, 1231 and 1251. 25 Compounds of the present invention and pharmaceutically acceptable saltss of said compounds that contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of the present invention. Isotopically-labeled compounds of the present invention, for example those into which radioactive isotopes such as 3 H, 14C are incorporated, are useful in drug and/or substrate tissue distribution 30 assays. Tritiated, i.e., 3 H, and carbon-14, i.e., 14C, isotopes are particularly preferred for their ease of preparation and detectability. "C and 8 F isotopes are particularly useful in PET (positron emission tomography), and 1251 isotopes are particularly useful in SPECT (single photon emission computerized tomography), all useful in brain imaging. Further, substitution with heavier isotopes such as deuterium, i.e., 2 H, 35 can afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements and, hence, 24 WO 2008/074821 PCT/EP2007/064185 may be preferred in some circumstances. Isotopically labelled compounds of formula (1) and following of this invention can generally be prepared by carrying out the procedures disclosed in the Schemes and/or in the Examples below, by substituting a readily available isotopically labelled reagent for a non-isotopically labeled reagent. 5 All publications, including but not limited to patents and patent applications, cited in this specification are herein incorporated by reference as if each individual publication were specifically and individually indicated to be incorporated by reference herein as though fully set forth. 10 The following Descriptions and Examples illustrate the preparation of compounds of the invention. Conditions, Hardware and Software for Analytical LCMS Systems 15 Hardware Agilent 1100 Gradient Pump Agilent 1100 Autosampler Agilent 1100 DAD Dectector Agilent 1100 Degasser 20 Agilent 1100 Oven Agilent 1100 Controller Waters Acquity Binary Solvent Manager Waters Acquity Sample Manager Waters Acquity PDA 25 Waters ZQ Mass Spectrometer Sedere Sedex 55, Sedere Sedex 85, Sedere Sedex 75 or Polymer Labs PL-ELS 2100 Software Waters MassLynx version 4.0 SP2 or version 4.1 30 For 5 minute method Column The column used is a Waters Atlantis, the dimensions of which are 4.6mm x 50mm. The stationary phase particle size is 3p.im. 35 Solvents A: Aqueous solvent = Water + 0.05% Formic Acid B : Organic solvent = Acetonitrile + 0.05% Formic Acid Method The generic method used has a 5 minute runtime. 40 Time/min %B 0 3 25 WO 2008/074821 PCT/EP2007/064185 0.1 3 4 97 4.8 97 4.9 3 5 5.0 3 Flow rate The above method has a flow rate of 3ml/mins For 2 minute method 10 Software Waters MassLynx version 4.1 Column 15 The column used is a Waters Acquity BEH UPLC C18, the dimensions of which are 2.1mm x 50mm. The stationary phase particle size is 1.7p. m. Solvents 20 A: Aqueous solvent = Water + 0.05% Formic Acid B : Organic solvent = Acetonitrile + 0.05% Formic Acid Weak Wash = 1:1 Methanol : Water Strong Wash = Water 25 Method The generic method used has a 2 minute runtime. Time / min %B 0 3 0.1 3 1.5 97 1.9 97 2.0 3 30 The above method has a flow rate of 1ml/min. The injection volume for the generic method is 0.5ul The column temperature is 40deg The UV detection range is from 220 to 330nm 35 26 WO 2008/074821 PCT/EP2007/064185 Open Access Mass Directed Auto Prep System (MDAP) Hardware Open Access Mass Directed Prep instruments consist of the following: 1 Waters 600 Gradient pump 5 1 Waters 2767 inject / collector 1 Waters Reagent manager 1 MicroMass ZQ Mass Spectrometer 1 Gilson Aspec - waste collector 1 Gilson 115 post-fraction UV detector 10 1 Computer System. Software MicroMass MassLynx v4.0 Column The column used is typically a Supelco LCABZ++ column whose dimensions are 15 20mm internal diameter by 100mm in length. The stationary phase particle size is 5pm. Solvents A:. Aqueous solvent = Water + 0.1% Formic Acid B:. Organic solvent = MeCN: Water 95:5 +0.05% Formic Acid 20 Make up solvent = MeOH: Water 80:20 +50mMol Ammonium Acetate Needle rinse solvent = MeOH: Water: DMSO 80:10:10 Methods One of five methods may be used depending on the analytical retention time of the compound of interest. 25 All have a 15-minute runtime, which comprises of a 10-minute gradient followed by a 5-minute column flush and re-equilibration step. MDP 1.5-2.2 = 0-30% B MDP 2.0-2.8 = 5-30% B MDP 2.5-3.0 = 15-55% B 30 MDP 2.8-4.0 = 30-80% B MDP 3.8-5.5 = 50-90% B Flow Rate All of the above methods have a flow rate of 20ml/min. 35 Alternative system:, Hardware - Waters 2525 Binary Gradient Module 40 - Waters 515 Makeup Pump - Waters Pump Control Module - Waters 2767 Inject Collect - Waters Column Fluidics Manager 27 WO 2008/074821 PCT/EP2007/064185 - Waters 2996 Photodiode Array Detector - Waters ZQ Mass Spectrometer - Gilson 202 fraction collector - Gilson Aspec waste collector 5 Software Waters MassLynx version 4 SP2 10 Column The columns used are Waters Atlantis, the dimensions of which are 19mm x 100mm (small scale) and 30mm x 100mm (large scale). The stationary phase particle size is 5m m. 15 Solvents A : Aqueous solvent = Water + 0.1% Formic Acid B : Organic solvent = Acetonitrile + 0.1% Formic Acid 20 Make up solvent = Methanol : Water 80:20 Needle rinse solvent = Methanol Methods 25 There are five methods used depending on the analytical retention time of the compound of interest. They have a 13.5-minute runtime, which comprises of a 10 minute gradient followed by a 3.5 minute column flush and re-equilibration step. Large/Small Scale 1.0-1.5 = 5-30% B 30 Large/Small Scale 1.5-2.2 = 15-55% B Large/Small Scale 2.2-2.9 = 30-85% B 35 Large/Small Scale 2.9-3.6 = 50-99% B Large/Small Scale 3.6-5.0 = 80-99% B (in 6 minutes followed by 7.5 minutes flush and re-equilibration) 40 Flow rate 28 WO 2008/074821 PCT/EP2007/064185 All of the above methods have a flow rate of either 20mls/min (Small Scale) or 40mls/min (Large Scale). Shallow gradients 5 Large 1.5 to 2.3 min = 13-29% B Large 1.9 to 2.3 min = 25-41% B Large 2.3 to 2.6 min = 37-53% B 10 Large 2.6 to 3.1 min = 49-65% B Large 3.1 to 3.6 min = 61-77% B 15 Conditions used for NMR Hardware Bruker 400MHz Ultrashield Bruker B-ACS60 Autosampler Bruker Advance 400 Console 20 Bruker DPX250 Bruker AVANCE 500 Bruker DRX600 Software User interface - NMR Kiosk 25 Controlling software - XWin NMR version 3.0 Chromatography Unless stated otherwise, all chromatography was carried out using silica columns 30 Abbreviations: g- grams mg - milligrams ml - millilitres 35 ul - microlitres MeCN - acetonitrile MeOH - methanol EtOH - ethanol Et 2 0 - diethyl ether 40 EtOAc - ethyl acetate DCM - dichloromethane 29 WO 2008/074821 PCT/EP2007/064185 DIAD - diisopropyl azodicarboxylate DME - 1,2-bis(methyloxy)ethane DMF - N,N-dimethylformamide DMSO - dimethylsulphoxide 5 EDAC - N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride EDC - N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride EDCI - N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride HOBT/HOBt - Hydroxybenzotriazole IPA - isopropylalcohol 10 NCS - N-chlorosuccinimide PyBOP - Benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate THF - tetrahydrofuran dba - dibenzylidene acetone RT - room temperature 15 OC- degrees Celsius M - Molar H - proton s- singlet d - doublet 20 t - triplet q - quartet MHz- megahertz MeOD - deuterated methanol LCMS - Liquid Chromatography Mass Spectrometry 25 LC/MS - Liquid Chromatography Mass Spectrometry MS - mass spectrometry ES - Electrospray MH* - mass ion + H* MDAP - mass directed automated preparative liquid chromatography. 30 sat. - saturated General chemistry section The intermediates for the preparation of the examples may not necessarily have 35 been prepared from the specific batch described. 30 WO 2008/074821 PCT/EP2007/064185 Description for D1 N-Hydroxy-1H-indole-5-carboximidamide (D1) HO, N

H

2 N H 5-Cyanoindole (1.00 g), hydroxylamine.HCI (978 mg) and NaHCO 3 (2.95 g) were 5 dissolved/suspended in MeOH (14 ml), heated to 50 'C and stirred overnight. LCMS analysis showed the reaction was incomplete after this time so a further portion of hydroxylamine.HCI (978 mg) was added and the reaction temperature raised to 80 'C. The reaction was complete after 4 hours. The reaction mixture was cooled to RT and evaporated to dryness under reduced pressure. The residue was treated with 10 1M aqueous HCI (50 ml) and extracted with EtOAc (2 x 50 ml). This failed to extract the product from the aqueous solution so it was treated with 2M aqueous NaOH to adjust the pH to approximately 7 then re-extracted with EtOAc (3 x 50 ml). The combined organics were washed with brine (30 ml), dried over MgSO 4 , filtered and evaporated to dryness to give the title compound (1.36 g) as a brown oil. 6H (MeOD, 15 400MHz) 6.50 (1H, s), 7.27 (1H, s), 7.36-7.45 (2H, m), 7.88 (1H, s). MS (ES):

C

9

H

8

N

3 0 requires 175; found 176 (MH*). Description for D2 5-{5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yI}-lH-indole (D2) O-N NN s N \/ N F 20 F F D1 (174 mg) and methyl 4-phenyl-5-(trifluoromethyl)-2-thiophenecarboxylate (286 mg) were combined, treated with sodium ethoxide (21 % wt in EtOH, 411 ul) and heated to 120 'C in a microwave reactor for 30 minutes. LCMS analysis showed the reaction was incomplete so microwave heating was continued for a further two 25 periods of 30 minutes. The reaction mixture was then cooled to RT, quenched with

H

2 0 (2 ml) and evaporated to dryness under reduced pressure to give the crude product (411 mg) as a brown solid. The crude residue was purified on a 40+S Biotage cartridge, eluting with a 0 to 50 % mixture of Et 2 0 in petroleum ether. This gave the title compound (122 mg) as an off-white solid. 6H (CDC13, 400MHz): 6.68 31 WO 2008/074821 PCT/EP2007/064185 (1H, s), 7.30 (1H, t), 7.41-7.55 (6H, m), 7.92 (1H, s), 7.99 (1H, d), 8.36 (1H, br. s), 8.50 (1H, s). MS (ES): C 2 1

H

1 2

F

3

N

3 0S requires 411; found 410 (M-H*). Description for D3 5 Ethyl 3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H indol-1 -yl)propanoate (D3) 0-N s N \/ NZ 0 FN F F D2 (100 mg) was dissolved in DMF (1.2 ml), treated with K 2

CO

3 (50 mg) then ethyl 3 bromopropionate (90 mg) and heated to 130 'C overnight. After this time LCMS 10 showed the reaction to be incomplete so further ethyl 3-bromopropionate was added (45 mg) and stirring continued at 130 'C for 2 hours. LCMS showed no change so the reaction mixture was evaporated then partitioned between DCM and H 2 0. The organic layer was removed and the aqueous solution extracted with DCM. The combined organics were dried over MgSO 4 , filtered and evaporated to give the crude 15 product (148 mg). This was purified on a silica cartridge (25+S), eluting with a 0 to 25 % mixture of EtOAc in petroleum ether and then again on a 25+M cartridge with a 0 to 30 % mixture of EtOAc in petroleum ether to give the title compound MF105672 144A3 (38 mg) as a white solid. 6H (CDC13, 400MHz): 1.21 (3H, t), 2.85 (2H, t), 4.12 (2H, q), 4.50 (2H, t), 6.60 (1H, d), 7.21 (1H, d), 7.42-7.52 (6H, m), 7.91 (1H, s), 8.00 20 (1H, d), 8.46 (1H, s). MS (ES*): C 2 6

H

2 0

F

3

N

3 0 3 S requires 511; found 512 (MH*). Description for D3 (Alternative procedure) Ethyl 3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H indol-1 -yl)propanoate (D3) 0-N - NN 0 F S F 25 F 5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1H-indole (D2) (600 mg), ethyl 3-bromopropanoate (374 pl), caesium carbonate (950 mg) and DMF were heated at 140 'C for 1 hour in a microwave reactor. A further 1 eq. of ethyl 3 bromopropanoate (187 pl) was added and the mixture heated for 30 minutes. The 32 WO 2008/074821 PCT/EP2007/064185 reaction mixture was then evaporated, dissolved in DCM and filtered to give the title compound (650 mg) as a brown solid. 6H (CDC13, 400MHz): 1.21 (3H, t), 2.85 (2H, t), 4.13 (2H, q), 4.50 (2H, t), 6.61 (1H, d), 7.22 (1H, d), 7.44-7.52 (6H, m), 7.89-7.92 (1H, m), 7.98-8.02 (1H, m), 8.45-8.46 (1H, m). MS (ES): C 2 6

H

2 0

F

3

N

3 0 3 S requires 5 511; found 512 (MH*). Description for D4 3-Chloro-4-[(1 -methylethyl)oxy]benzoic acid (D4) 0 ' OH 0e0 Propan-2-ol (2.45 ml) and PPh 3 (1.18 g) were dissolved in THF (30 ml), cooled to 0 10 'C, treated with methyl 3-chloro-4-hydroxybenzoate (6.00 g) followed by the drop wise addition of DIAD (9.44 ml) and stirred at RT overnight. The reaction mixture was then evaporated and purified on silica cartridges (4 x 100 g), eluting with a 0 to 40 % mixture of EtOAc in pentane to give the crude product (7.00 g) as a colourless oil. This was dissolved in MeOH (30 ml) and 2 M aqueous NaOH (30 ml) and stirred at 15 RT for a weekend. The reaction mixture was then evaporated and re-dissolved in

H

2 0. This solution was washed with Et 2 0, acidified to pH = 1 and extracted with Et 2 0. These latter extracts were dried over MgSO 4 , filtered and evaporated to give the title compound (4.16 g) as a white solid. 6H (MeOD, 400MHz): 1.37 (6H, d), 4.77 (1H, septet), 7.12 (1H, d), 7.90 (1H, d), 7.98 (1H, s). MS (ES): C 10

H

11 CI0 3 requires 20 214; found 215 (MH*). Alternative synthesis: 3-Chloro-4-[(1-methylethyl)oxy]benzoic acid (D4) 0 "' OH 0e0 25 Methyl-4-hydroxy-3-chloro benzoate (13.4 g) was dissolved in DMF (150 ml), treated with K 2

CO

3 (19.9 g) followed by isopropyl bromide (13.5 ml) and the resultant mixture heated to 70 'C and stirred overnight. The reaction mixture was then cooled to RT, evaporated to dryness, re-dissolved in EtOH, filtered and evaporated once more to give the intermediate ester (22.2 g) as a white solid. This compound was a mixture of 30 ethyl and methyl esters and used crude in the next reaction. 33 WO 2008/074821 PCT/EP2007/064185 The crude intermediate (22.2 g) was dissolved in MeOH (75 ml), treated with 2M aqueous NaOH (75 ml), heated to 60 'C and stirred for 2 hours. The reaction mixture was then cooled to RT, the MeOH evaporated and the remaining aqueous solution acidified with 5M aqueous HCI (30 ml). The precipitate was filtered off and dried to 5 give the title compound (15.1 g) as a white solid. 6H (CDC13, 400MHz): 1.42 (6H, d), 4.70 (1H, septet), 6.97 (1H, d), 7.97 (1H, d), 8.12 (1H, s). MS (ES): C 10

H

11 CI0 3 requires 214; found 213 (M-H*). Description for D5 MF105672-175A2 10 5-(5-{3-Chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indole (D5) CI O-N O N D1 (500 mg), D4 (611 mg) and PyBOP (1.66 g) were dissolved in DMF and stirred overnight. The reaction mixture was then evaporated and partitioned between EtOAc 15 and H 2 0. The organic layer was washed with H 2 0 (x 2) then brine, dried over MgSO 4 , filtered and evaporated to give the crude product. This was purified on a silica cartridge, eluting with a 0 to 50 % mixture of Et 2 0 in hexane to give the title compound (120 mg) as a white solid. 6H (CDC13, 400MHz): 1.43 (6H, d), 4.69 (1H, septet), 6.92 (1H, s), 7.04 (1H, d), 7.25 (1H, s), 7.48 (1H, d), 8.00 (1H, d), 8.07 (1H, 20 d), 8.25 (1H, s), 8.39 (1H, br. s), 8.50 (1H, s). MS (ES): C1 9

H

1

CIN

3 0 2 requires 353; found 354 (MH*). Description for D5 (alternative procedure) 5-(5-{3-Chloro-4-[(1 -methylethyl)oxy]phenyl}- 1,2,4-oxadiazol-3-yl)-1 H-indole 25 (D5) CI 0-N O N A mixture of 5-cyanoindole (5.00 g), NH 2 OH.HCI (6.11 g) and NaHCO 3 (14.77 g) in 30 EtOH (176 ml) was heated at 70 'C under an atmosphere of Ar overnight and then at 80 'C for 2.5 hours. The reaction mixture was then filtered and evaporated to give a yellow-orange solid (crude material D1). 34 WO 2008/074821 PCT/EP2007/064185 D4 (7.55 g), HOBT (5.23 g) and EDCI (7.42 g) were dissolved in DMF (88 ml). This mixture was stirred for 10 minutes and then the yellow-orange solid from above (6.16 g) dissolved in DMF (88 ml) was added. The reaction mixture was heated to 80 'C overnight then evaporated and partitioned between EtOAc and H 2 0. The phases 5 were separated and the aqueous solution extracted with two further portions of EtOAc. The combined organic solutions were dried and evaporated. Part of the crude residue was purified on a 40+M Biotage cartridge, eluting with a 5-30 % mixture of EtOAc in hexane. This gave the title compound (1.45 g) as an off-white solid. 6H (CDC13, 400MHz): 1.45 (6H, d), 4.72 (1H, septet), 6.66-6.69 (1H, m), 7.06 (1H, d), 10 7.29 (1H, apparent triplet or dd), 7.50 (1H, d), 8.01 (1H, dd), 8.08 (1H, dd), 8.27 (1H, d), 8.49-8.52 (1H, m). MS (ES): C 19

H

16

CIN

3 0 2 requires 353; found 354 (MH*). The remaining crude reside was triturated with cold MeOH to give the title compound (3.54 g) as an off white solid. MS data as above. 15 Description for D6 Ethyl 3-[5-(5-{3-chloro-4-[(1 -methylethyl)oxy] phenyl}-1,2,4-oxadiazol -3-yl)-1 H indol-1 -yl]propanoate (D6) ci O-N N N 0 D5 (100 mg) was dissolved in DMF (1.5 ml). To this solution was added K 2

CO

3 (58 20 mg) followed by ethyl 3-bromopropionate (72 ul) and the mixture stirred and heated to 100 'C. After 1 hour only 5 % conversion was observed by LCMS so further portions of K 2

CO

3 (97 mg) and ethyl 3-bromopropionate (72 ul) were added. After 3 hours the reaction mixture was evaporated then partitioned between DCM and H 2 0. The aqueous layer was extracted with DCM then the combined DCM solutions were 25 washed with brine, dried over MgSO 4 , filtered and evaporated to give the crude product. This was purified on a silica cartridge, eluting with a 0 to 50 % mixture of Et 2 0 in petroleum ether. This gave the title compound (40 mg) as a white solid. 6H (CDC13, 400MHz): 1.21 (3H, t), 1.45 (6H, d), 2.85 (2H, t), 4.13 (2H, q), 4.51 (2H, t), 4.71 (1H, septet), 6.60 (1H, d), 7.07 (1H, d), 7.21 (1H, d), 7.45 (1H, d), 8.02 (1H, d), 30 8.08 (1H, d), 8.27 (1H, s), 8.47 (1H, s). MS (ES): C 24

H

24

CIN

3 0 4 requires 453; found 454 (MH*). Description for D7 35 WO 2008/074821 PCT/EP2007/064185 3-Chloro-5-(5-{3-chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-y)-1 H indole (D7) ci 0-N -N 0 N 5 D5 (300 mg) and NCS (113 mg) were dissolved in DCM (4.2 ml) and stirred overnight at room temperature. The reaction mixture was then diluted with DCM and washed with H 2 0. The aqueous solution was extracted with two further portions of DCM and the combined organic solutions were evaporated to dryness. The crude product was triturated with methanol to give the title compound (42 mg) as a brown 10 solid. The methanol was then evaporated and the resultant brown solid triturated with DCM to give a second batch of the title compound (205 mg) as a brown solid. 6H (d 6 DMSO, 400MHz): 1.37 (6H, d), 4.89 (1H, septet), 7.45 (1H, d), 7.62 (1H, d), 7.70 (1H, s), 7.93 (1H, d), 8.15 (1H, d), 8.24 (1H, s), 8.25 (1H, s), 11.77 (1H, s). MS (ES):

C

1 9

H

15 35 C1 2

N

3 0 2 requires 387; found 388 (MH*). 15 Description for D8 3-Chloro-5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yI}-1 H indole (D8) CI 0-N N \ s H F F F 20 D2 (200 mg) and NCS (65 mg) were dissolved in DCM (5 ml) and stirred overnight at room temperature. The reaction mixture was then partitioned between DCM and

H

2 0. The DCM solution was evaporated to dryness and purified on a Biotage silica cartridge, eluting with a 25-75 % mixture of diethyl ether in hexane. This gave the title 25 compound (36 mg) as a brown solid. A second batch of the title compound was also obtained from this purification (86 mg) as a brown solid. 6H (CDCl 3 , 400MHz): 7.28 (1H, m), 7.45-7.54 (6H, m), 7.93 (1H, s), 8.05 (1H, d), 8.28 (1H, br s), 8.49 (1H, s). MS (ES): C 21

H

11

CIF

3

N

3 0S requires 445; found 444 (M-H*). 30 Desciption 9 36 WO 2008/074821 PCT/EP2007/064185 N-Hydroxy-1H-indole-4-carboximidamide (D9) HO-N NH

H

2 N 4-Cyanoindole (850 mg) was dissolved in EtOH (25 ml). To this solution was added NaHCO 3 (2.51 g) and NH 2 OH.HCI (831 mg). The mixture was heated to 70 'C and 5 stirred overnight. The reaction was incomplete so was heated at 80 'C for a further 4 hours. The reaction mixture was filtered and evaporated to give the title compound (980 mg) as a yellow semisolid. No purification attempted. Description for D9 (alternative procedure) 10 N-Hydroxy-1H-indole-4-carboximidamide (D9) OH N-.. N N 15 A mixture of 4-cyanoindole (5.0g, 35.2 mmol), sodium hydrogen carbonate (8.9g, 105.6 mmol) and hydroxylamine hydrochloride (4.9g, 70.4 mmol) in ethanol (200ml) was heated at 55 0C overnight. Sodium hydrogen carbonate (5.9g, 70 mmol) and hydroxylamine hydrochloride (4.9g, 70.4 mmol) was added. The mixture was heated 20 for 4 days until only a small amount of starting material was present. The inorganics were filtered off, washing the solid well with ethanol and evaporated off the solvent. The residue was triturated with diethyl ether to give 5.8g of off-white solid. 6H (400 MHz, methanol-d 4 ) 6.76-6.78 (1H, m), 7.12 (1H, t), 7.24 (1H, dd), 7.29-7.33 (1H, m) 7.46 (1H, dd). 25 Description for D10 4-{5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-y}-1H-indole (D1O) 37 WO 2008/074821 PCT/EP2007/064185 O-N NH N F S F F 4-Phenyl-5-(trifluoromethyl)-2-thiophenecarboxylic acid (310 mg), HOBT (170 mg) and EDCI.HCI (242 mg) were dissolved in DMF (3 ml) and stirred at room temperature for 20 mins. D9 (200 mg) was dissolved in DMF (3 ml) and added to the 5 above solution and stirring continued at room temperature for two hours. The reaction mixture was then heated to 90 'C, cooled to RT, stood overnight, re-heated to 80 'C and stirred for 3 hours, cooled to room temperature and evaporated to dryness. The residue was re-dissolved in H 2 0 and extracted with EtOAc (x 3) and the combined organic extracts evaporated to dryness. The residue was purified by 10 flash silica chromatography, eluting with a 25-75 % mixture of diethyl ether in hexane to give the title compound (265 mg) as a brown solid. A sample of this compound (100 mg) was purified by MDAP to give the title compound (62 mg) as an off white solid. 6H (CDC13, 400MHz): 7.33-7.36 (2H, m), 7.41-7.42 (1H, m), 7.46-7.52 (5H, m), 7.61 (1H, d), 7.94 (1H, s), 8.06 (1H, d), 8.46 (1H, br s). MS (ES): C 21

H

12

F

3

N

3 0S 15 requires 411; found 412 (MH*). Description for D11 Ethyl 3-bromo-2,2-dimethylpropanoate (D11) 0 Br O 20 3-Bromo-2,2-dimethylpropanoic acid (200 mg) was dissolved in EtOH (5 ml) and treated with concentrated H 2

SO

4 (0.4 ml). This mixture was heated at reflux overnight then evaporated. The residue was extracted from H 2 0 with EtOAc (x 2) and the combined organic solutions dried and evaporated to give the title compound (316 mg) as a clear oil. 6H (CDC13, 400MHz) 1.20 (3H, t), 1.32 (6H, s), 3.51 (2H, s), 4.18 25 (2H, q). Description for D12 3-Ethyl-4-(1 -piperidinyl)benzonitrile (D1 2) 38 WO 2008/074821 PCT/EP2007/064185 CN N 4-Amino-3-ethylbenzonitrile (3.0 g, 20.5 mmol), 1,5-dibromopentane (11.1 mL, 82.1 mmol), potassium carbonate (5.67 g, 41.0 mmol) and water (39.6 mL) were all split equally between ten microwave vials and each heated at 160 'C for 1 h. All reaction 5 mixtures were combined and extracted twice with ethyl acetate (40 mL) and the combined organic fractions dried (phase separator) and concentrated in vacuo. Dichloromethane was added and then the mixture filtered before the filtrate was purified by silica chromatography, eluting 2-5 % ethyl acetate in hexane to give the title compound as a colourless oil (823 mg, 3.85 mmol). Analysis indicated that the 10 compound contained a small dibromopentane impurity. 6H (methanol-d 4 , 400 MHz) 7.52 (1H, dd), 7.47 (1H, dd), 7.13 (1H, d), 2.89 (4H, dd), 2.71 (2H, q), 1.76-1.71 (4H, m), 1.64-1.56 (2H, m), 1.25 (3H, t). MS (ES): C 14

H

1 8

N

2 requires 214; found 215 (MH*). 15 Description for D13 3-Ethyl-4-(1 -piperidinyl)benzoic acid (D1 3)

CO

2 H N 3-ethyl-4-(1-piperidinyl)benzonitrile (D12) (817 mg, 3.82 mmol) and potassium hydroxide (2.14 g, 38.2 mmol) in ethanol (35 mL) and water (8 mL) were heated to 20 90 'C (block temperature) for 9 h. Further potassium hydroxide (2.14 g, 38.2 mmol) and water (8 mL) were added and the reaction heated for a further 18 h. The reaction was allowed to cool and was neutralised with aqueous HCI. A white solid was collected by filtration and an attempt was made to purify the filtrate by SCX cartridge, but this failed. Both the solid and product of SCX were combined, 39 WO 2008/074821 PCT/EP2007/064185 methanol added and then the mixture acidified with acetic acid. The mixture was filtered to obtain the filtrate, which was then trapped on SCX cartridge, washed with methanol and eluted with 2M ammonia in methanol. On test scale this gave the title compound as a white solid (96 mg, 0.41 mmol) and on the remaining material gave a 5 colourless oil (563 mg, 2.41 mmol). 6H (methanol-d 4 , 400 MHz): 7.85 (1H, d), 7.74 (1H, dd), 7.03 (1H, d), 2.85 (4H, dd), 2.73 (2H, q), 1.72 (4H, m), 1.61 (2H, m), 1.25 (3H, t) ppm. MS (ES): C 14

H

1 9

NO

2 requires 233; found 234 (MH*). Description for D14 10 Ethyl 5-chloro-6-(1 -pyrrol idi nyl)-3-pyridi necarboxylate (D14) 0 Cl N N A mixture of 5,6-dichloronicotinic acid ethyl ester (1.00 g, 4.57 mmol), pyrrolidine 15 (325 mg, 4.57 mmol), potassium carbonate (632 mg, 4.57 mmol) and copper powder (34 mg) in DMF (6.8 mL) was heated at 130 'C in the microwave for 20 min. Further pyrrolidine (163 mg, 2.29 mmol) was added and the reaction heated at 130 'C for 20 min. Water (7 mL) was added and the mixture extracted with ethyl acetate (2 x 14 mL). The combined organic extracts were washed with water (7 mL) and brine (7mL) 20 before being dried (phase separator) and concentrated in vacuo to give the title compound as an orange oil (1.06 g, 4.17 mmol). 6H (methanol-d 4 , 400 MHz): 8.45 (1H, d), 7.98 (1H, d), 4.31 (2H, q), 3.82-3.75 (4H, m), 2.0-1.93 (4H, m), 1.36 (3H, t) ppm. MS (ES): C 1 2

H

15

CIN

2 0 2 requires 254, 256; found 255, 257 (MH*). 25 Description for D15 5-Chloro-6-(l-pyrrolidinyl)-3-pyridinecarboxylic acid (D15) 0 Cl OH

K

N N 40 WO 2008/074821 PCT/EP2007/064185 Ethyl 5-chloro-6-(1-pyrrolidinyl)-3-pyridinecarboxylate (D14) (1.06 g, 4.16 mmol) in ethanol (20 mL) and aqueous sodium hydroxide (2M, 2.08 mL, 4.16 mmol) was heated at 40 'C for 18 h. The reaction mixture was allowed to cool and was neutralised with 2M HCI (aq.). The title compound formed as a white solid and was 5 filtered off and washed with methanol to give the title compound (243 mg, 1.08 mmol) SJ108923-113A3. The filtrate was trapped on an SCX column, eluting with 2M ammonia in methanol to give further title compound as an orange solid (467 mg, 2.07 mmol). 6H (methanol-d 4 , 400 MHz): 8.55 (1H, d), 8.03 (1H, d), 3.76-3.70 (4H, m), 1.96-1.90 (4H, m). MS (ES): C 10

H

11

CIN

2 0 2 requires 226, 228; found 227, 229 (MH*). 10 Description for D16 3-Ethyl-4-iodobenzonitrile (D16) CN To 4-amino-3-ethylbenzonitrile (2.50 g, 17.1 mmol) stirred in water (14 mL) at 0 'C 15 was added concentrated hydrochloric acid (7.80 mL, 257 mmol) dropwise followed by a solution of sodium nitrite (1.24 g, 18.0 mmol) in water (3.43 mL) dropwise. The resultant mixture was stirred for 15 minutes and then added over 15 minutes to a solution of potassium iodide (2.98 g, 18.0 mmol) in water (6.0 mL) at 0 'C. The mixture was stirred at room temperature for 2 h. The mixture was extracted with 20 ethyl acetate (3 x 100 mL) and the combined organic fractions washed with brine (100 mL), dried (phase separator) and concentrated in vacuo to give the title compound as a brown solid (4.21 g, 16.4 mmol). 6H (methanol-d 4 , 400 MHz): 8.02 (1H, d), 7.61 (1H, d), 7.24 (1H, dd), 2.80 (2H, q), 1.21 (3H, t). MS (ES): No mass ion observed. 25 Description for D17 4-(l-Cyclohexen-1-yI)-3-ethylbenzonitrile (D17) 41 WO 2008/074821 PCT/EP2007/064185 CN A mixture of 3-ethyl-4-iodobenzonitrile (D16) (1.23 g, 4.80 mmol), 1-cyclohexen-1 ylboronic acid (907 mg, 7.20 mmol), sodium methoxide (778 mg, 14.4 mmol) and bis(triphenylphosphine)palladium (II) chloride (337 mg, 0.48 mmol) in anhydrous 5 methanol (12 mL) was heated at 80 'C for 10 minutes in the microwave. The reaction mixture was partitioned between ethyl acetate (40 mL) and water (40 mL) before the organic layer was further washed with water (40 mL), dried (phase separator) and concentrated in vacuo. The crude material was purified by silica chromatography, eluting 0-5 % EtOAc in hexane over 30 minutes to give the title 10 compound as a yellow oil (824 mg, 3.91 mmol). 6H (methanol-d 4 , 400 MHz) 7.56 (1H, d), 7.46 (1H, dd), 7.19 (1H, d), 5.61-5.56 (1H, m), 2.68 (2H, quart), 2.23-2.16 (4H, m), 1.85-1.68 (4H, m), 1.20 (3H, t). MS (ES): No mass ion observed. Description for D18 15 4-(1-Cyclohexen-1-yI)-3-ethylbenzoic acid (D18)

CO

2 H 4-(1-cyclohexen-1-yl)-3-ethylbenzonitrile (D17) (824 mg, 3.91 mmol) and potassium hydroxide (2.19 g, 39.1 mmol) in ethanol (36 mL) and water (8 mL) were heated at 90 'C (block temperature) for 20 h. The reaction mixture was concentrated in vacuo 20 and the residue partitioned between ethyl acetate (120 mL) and aqueous hydrochloric acid (2M, 50 mL) before the organic phase was washed with further hydrochloric acid (2M, 50 mL), dried (phase separator) and concentrated in vacuo to give the title compound as a yellow oil (808 mg, 3.51 mmol). 6H (methanol-d 4 , 400 42 WO 2008/074821 PCT/EP2007/064185 MHz) 7.87 (1H d), 7.76 (1H dd), 7.11 (1H, d) 5.59-5.54 (1H, m), 2.68 (2H, q), 2.25 2.15 (4H, m), 1.84-1.67 (4H, m), 1.20 (3H, t). LCMS (ES): C 15

H

18 0 2 requires 230; found 229 (M-H*). 5 Description for D19 4-Cyclohexyl-3-ethylbenzoic acid (D19)

CO

2 H 4-(1-cyclohexen-1-yl)-3-ethylbenzoic acid (D18) (803 mg, 3.49 mmol) was dissolved 10 in methanol (70 mL) and hydrogenated on an H-Cube using a palladium on carbon cartridge. The product solution was concentrated in vacuo to give the title compound as a white solid (792 mg, 3.41 mmol). 6H (methanol-d 4 , 400 MHz): 7.82-7.68 (2H, m), 7.33 (1H, d), 2.83 (1H, m), 2.73 (2H, q), 1.87 (2H, m), 1.85-1.70 (3H, m), 1.58 1.30 (5H, m), 1.22 (3H, t). LCMS (ES): no mass ion observed. 15 Description for D20 1 -Methylethyl 3-bromo-4-[(l -methylethyl)oxy]benzoate (D20) o 0 Br 0 A mixture of 3-bromo-4-hydroxybenzoic acid (2.00 g, 9.22 mmol), 2-iodopropane 20 (1.85 mL, 18.4 mmol) and potassium carbonate (2.55 g, 18.4 mmol) in DMF (175 mL) was heated to reflux for 5 h. The reaction was allowed to cool and was filtered. The filtrate was concentrated in vacuo and the residue partitioned between ethyl acetate (150 mL) and water (150 mL), which was basified with 2M NaOH. The 43 WO 2008/074821 PCT/EP2007/064185 organic phase was dried (phase separator) and concentrated in vacuo to give the title compound as a yellow oil (2.36 g, 7.84 mmol). 6H (methanol-d 4 , 400 MHz): 8.05 (1H, d), 7.90 (1H, dd), 7.25 (1H, d), 5.10 (1H, septet), 4.81 (1H, septet), 1.32 (6H, d), 1.31 (6H, d) ppm. MS (ES): no mass ion observed. 5 Description for D21 3-Bromo-4-[(1 -methylethyl)oxy] benzoic acid (D21) 0 OH Br 0 10 A solution of 1-methylethyl 3-bromo-4-[(1 -methylethyl)oxy]benzoate (D20) (2.36 g, 7.84 mmol) in ethanol (100 mL) and aqueous sodium hydroxide (2M, 39 mL) was heated to reflux for 5 h. The reaction mixture was concentrated in vacuo and partitioned between ethyl acetate (125 mL) and water (125 mL), the latter acidified 15 with 2M HCI (40 mL). The aqueous layer was extracted with further ethyl acetate (70 mL) and the combined organic extracts dried (phase separator) and concentrated in vacuo to give the title compound as an off-white solid (1.83 g, 7.06 mmol). 6H (methanol-d 4 , 400 MHz): 8.05 (1H, d), 7.89 (1H, dd), 7.23 (1H, d), 4.79 (1H, septet), 1.32 (6H, d). MS (ES): C 10

H

11 BrO 3 requires 258, 260; found 257, 259 (M-H*). 20 Description for D22 Ethyl 4-bromo-3-chlorobenzoate (D22) O o CI Br 25 44 WO 2008/074821 PCT/EP2007/064185 To a suspension of 4-bromo-3-chlorobenzoic acid (5.00 g, 21.2 mmol) in ethanol (50 mL) was added sulphuric acid (5 mL) and the resultant mixture heated to reflux for 60 h. The reaction was partitioned between ethyl acetate (50 mL) and water (50 mL). The aqueous layer was extracted with further ethyl acetate and the combined organic 5 fractions dried (phase separator) and concentrated in vacuo to give the title compound as a brown oil/solid (5.09 g, 19.3 mmol). 6H (d 6 -DMSO, 400 MHz): 8.06 (1H, d), 7.96 (1H, d), 7.80 (1H, dd), 4.33 (2H, q), 1.33 (3H, t). MS (ES): no mass ion observed. 10 Description for D23 Ethyl 3-chloro-4-(2-methylpropyl)benzoate (D23) o O Cl A solution of isobutylzinc bromide in THF (0.5 M, 30 mL, 15.0 mmol) was added under argon to ethyl 4-bromo-3-chlorobenzoate (D22) (2.00 g, 7.60 mmol) and then 15 1,1'-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (930 mg, 1.14 mmol) was added. The reaction was heated to reflux for 4.5 h. The mixture concentrated in vacuo and the residue partitioned between ethyl acetate (125 mL) and water (125 mL). A solid formed, which was filtered off and discarded. The organic layer was washed with water (100 mL), dried (phase 20 separator) and concentrated in vacuo. The crude product was purified by silica chromatography, eluting with 0-5 % EtOAc in hexane over 30 minutes to give the title compound as a colourless oil (1.76 g, 7.33 mmol). 6H (d 6 -DMSO, 400 MHz): 7.91 (1H,d), 7.80 (1H, dd), 7.46 (1H, d), 4.30 (2H, q), 2.66 (2H, d), 1.88-2.01 (1H, m), 1.32 (3H, t), 0.89 (6H, d). MS (ES): no mass ion observed. 25 Description for D24 3-Chloro-4-(2-methylpropyl)benzoic acid (D24) 45 WO 2008/074821 PCT/EP2007/064185 0 OH C A solution of ethyl 3-chloro-4-(2-methylpropyl)benzoate (D23) (1.76 g, 7.33 mmol), and aqueous sodium hydroxide (2M, 3.70 mL, 7.4 mmol) in ethanol (30 mL) was heated at 40 'C for 3 h. The reaction mixture was concentrated in vacuo and the 5 residue partitioned between ethyl acetate (100 mL) and water (100 mL), the latter acidified with 2M HCI (4 mL). The aqueous layer was extracted with ethyl acetate (100 mL) and the combined organic extracts dried (phase separator) and concentrated in vacuo to give the title compound as a white solid (1.35 g, 6.36 mmol). 6H (d 6 -DMSO, 400 MHz): 13.20 (1H, br. s), 7.89 (1H, d), 7.82 (1H, dd), 7.44 10 (1H, d), 2.64 (2H, d), 1.94 (1H, m), 0.89 (6H, d). MS (ES): C 11

H

1 3 35 CI0 2 requires 212; found 211 (M-H*). Description for D25 Methyl 3-cyano-4-{[(trifluoromethyl)sulfonyl]oxy}benzoate (D25) 15 O S

F

3 C 0 To a solution of methyl 3-cyano-4-hydroxybenzoate (3 g, 16.93 mmol) and triethylamine (3.54 ml, 25.4 mmol) in dry dichloromethane (60 ml) at 0 0C under a 20 flush of argon was added trifluoromethanesulfonic anhydride (3.15 ml, 18.63 mmol) slowly dropwise. The reaction was allowed to warm to room temperature and stirred for 1 h. The reaction mixture was washed with 10 % aqueous potassium carbonate (2 x 50 mL) and then aqueous HCI (2M, 2 x 50 mL) before the organic phase was 46 WO 2008/074821 PCT/EP2007/064185 dried (phase separator) and the solvent removed in vacuo to give the title compound as a dark brown oil, (5.165 g, 16.70 mmol). 6H (CDC13, 400 MHz): 8.44 (1H, d), 8.38 (1H, dd), 7.60 (1H, d), 3.99 (3H, s). MS (ES): no mass ion observed. 5 Description for D26 Methyl 2-cyano-4-biphenylcarboxylate (D26) O O0 The following reaction was split into two batches with half the amounts: methyl 3 cyano-4-{[(trifluoromethyl)sulfonyl]oxy}benzoate (D25) (1.5 g, 4.85 mmol), 10 phenylboronic acid (1.183 g, 9.70 mmol), potassium carbonate (2.011 g, 14.55 mmol) and palladium tetrakistriphenylphosphine(0) (0.561 g, 0.485 mmol) were taken up in DMF (24 ml) and the mixture heated in the microwave for 30 min at 150 0C. The two reactions were combined and diluted with ethyl acetate (50 mL) and the mixture filtered through kieselguhr to remove palladium residues. The filtrate was 15 concentrated in vacuo to reduce the amount of DMF and then the residue partitioned between saturated aqueous sodium bicarbonate (50 mL) and ethyl acetate (50 mL). The organic phase was washed with further sodium bicarbonate (50 mL) and then water (50 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The brown solid was purified by silica chromatography, eluting 0-25 % EtOAc 20 in iso-hexane over 35 minutes to give the title compound as a white solid (935 mg, 3.94 mmol). 6H (d 6 -DMSO, 400 MHz): 8.42 (1H, d), 8.29 (1H, dd), 7.81 (1H, d), 7.65 (2H, m), 7.60 -7.50 (3H, m), 3.92 (3H, s). MS (ES): no mass ion observed. Description for D27 25 2-Cyano-4-biphenylcarboxylic acid (D27) 47 WO 2008/074821 PCT/EP2007/064185 O OH To methyl 2-cyano-4-biphenylcarboxylate (D26) (935 mg, 3.94 mmol) was added ethanol (18 ml) but dissolution did not occur so dichloromethane (10 ml) was added. Sodium hydroxide (2 ml, 4.00 mmol) was then added and the reaction stirred for 2 h. 5 To the mixture was added dichloromethane (20 mL) and 2M aqueous HCI (10 mL). The layers were separated and the aqueous extracted with further dichloromethane (20 mL). The combined organic phase was dried (phase separator) and the solvent removed in vacuo to give a white solid, which was dissolved in methanol (30 mL) and aqueous sodium hydroxide was added (2M, 3 mL). The reaction was stirred at room 10 temperature for 1 h before addition of water (20 mL). The reaction was stirred for a further 1h. Dichloromethane (60 mL) was added and the mixture shaken and the layers separated. The aqueous phase was extracted with further dichloromethane (50 mL) before the combined organic phase was dried (phase separator) and the solvent removed in vacuo to give the title compound as a white solid, (849 mg, 3.80 15 mmol). 6H (d 6 -DMSO, 400 MHz): 13.60 (1H, br s), 8.38 (1H, d), 8.28 (1H, dd), 7.78 (1H, d), 7.63 (2H, m), 7.60-7.50 (3H, m). MS (ES): C 14

H

9

NO

2 requires 223; found 222 (M-H*). Description for D28 20 Ethyl 4-chloro-3-(trifluoromethyl)benzoate (D28) O O

CF

3 Cl 4-Chloro-3-(trifluoromethyl)benzoic acid (1 g, 4.45 mmol) was dissolved in ethanol (3 ml) and concentrated sulfuric acid (0.15 ml) was added. The mixture was heated in 48 WO 2008/074821 PCT/EP2007/064185 the microwave at 100 'C for 5 minutes and then 120 'C for 15 minutes. The solvent was removed in vacuo and the residue partitioned between saturated aq. sodium bicarbonate (50 ml) and ethyl acetate (50 ml). The aqueous layer was extracted with further EtOAc (50 ml) and the organic phases were combined, dried with a phase 5 separator and concentrated in vacuo to give the title compound (1.026 g) (DN108121-148A3) as a colourless oil. 6H (methanol-d 4 , 400 MHz) 1.40 (3H, t), 4.41 (2H, q), 7.76 (1H, d), 8.21 (1H, dd), 8.33 (1H, d). MS (ES) no mass ion observed. Description for D29 10 2-(Trifluoromethyl)-4-biphenylcarboxylic acid (D29) O OH

CF

3 The reaction was split into 4, using a quarter of the reagents in each: to a mixture of 4-bromo-3-(trifluoromethyl)benzonitrile (4 g, 16.00 mmol), phenylboronic acid (3.90 g, 32.0 mmol) and potassium carbonate (6.63 g, 48.0 mmol) in N,N-dimethylformamide 15 (DMF) (64 ml) was added palladium tetrakistriphenylphosphine(0) (1.849 g, 1.600 mmol). Each reaction was heated in the microwave at 150 0C for 30 min. The combined reaction mixtures were filtered through celite, washed with ethyl acetate and the solvent removed in vacuo. The residue was partitioned between ethyl acetate (100 mL) and water (100 mL) and the organic phase washed with sodium 20 bicarbonate solution (100 mL). The organic phase was dried (MgSO4), filtered and the solvent removed in vacuo. The brown oil was triturated with dichloromethane and filtered to give a pale yellow solid, 2-(trifluoromethyl)-4-biphenylcarboxamide (2.47 g) which was used without further purification. To 2-(trifluoromethyl)-4 biphenylcarboxamide (2 g, 7.54 mmol) in ethanol (80 ml) was added potassium 25 hydroxide (4.23 g, 75 mmol) and water and the mixture heated to 90 0C for 18 h. The reaction mixture was concentrated in vacuo and the residue partitioned between dichloromethane (100 mL) and 2M HCI (100 mL). The organic phase was isolated and dried (phase separator) and the solvent removed in vacuo to give the crude product. Purification using the Biotage Horizon, reverse phase cartridge, eluting 5 49 WO 2008/074821 PCT/EP2007/064185 100 % MeCN in water to give an off-white solid the title compound (960 mg) (N2123 46-A5). MS (ES): C 14

H

9

F

3 0 2 requires 266; found 265 (M-H*). Description for D29 (Alternative procedure) 5 2-(Trifluoromethyl)-4-biphenylcarboxylic acid (D29) 0 OH

CF

3 Batch A: A mixture of D98 (1.0 g, 3.96 mmol), phenyl boronic acid (724 mg, 5.94 mmol), palladium acetate (44 mg), (dicyclohexylphosphino)biphenyl (140.2 mg) and potassium fluoride (689 mg, 11.9 mmol) in THF (8 ml) was heated in the microwave 10 at 120 'C for a total of 40 minutes. Batch B: A mixture of D28 (500 mg, 1.98 mmol), phenyl boronic acid (290 mg, 2.38 mmol), palladium acetate (2.2 mg), (dicyclohexylphosphino)biphenyl (7 mg) and potassium fluoride (344 mg, 5.8 mmol) in THF (4 ml) was heated in the microwave at 120 'C for 20 minutes. 15 The reaction mixtures from batches A & B were combined, filtered and the filtrate concentrated in vacuo. The residue was purified by flash chromatography (0 to 5% EtOAc in hexane to give a mixture of starting material and coupled product. This material was dissolved in ethanol (10 ml) and 2M NaOH (aq) (5ml) and then heated to reflux for 3 h. The solvent was removed in vacuo and the residue partitioned 20 between DCM and 2M aq. HCI. The aq. was extracted with further DCM. The organic phases were combined and concentrated in vacuo. The crude material was purified by reversed phase chromatography on the Horizon eluting with 5 to 100% MeCN in water to afford the title compound as a white solid (367 mg) . 6H (d 6 -DMSO, 400 MHz) 7.31-7.40 (2H, m), 7.44-7.52 (3H, m), 7.57 (1H, d), 8.24 (1H, dd), 8.29 (1H, d), 25 13.57 (1H, br. s). MS (ES): C 14

H

9

F

3 0 2 requires 266; found 265 (M-H*). Description for D30 2'-Fluoro-2-(trifluoromethyl)-4-biphenylcarboxylic acid (D30 50 WO 2008/074821 PCT/EP2007/064185 0 OH

CF

3 F This material was prepared using a similar method to that described for D29 using (2-fluorophenyl)boronic acid and D98 except that only a single coupling reaction was performed, similar to batch A and the coupling reaction was heated for 20 minutes. 5 MS (ES): C 14

H

8

F

4 0 2 requires 284; found 283 (M-H*). Description for D31 Methyl 3-cyano-4-(2-methylpropyl)benzoate (D31) O1 0 N 10 To methyl 3-cyano-4-{[(trifluoromethyl)sulfonyl]oxy}benzoate (D25) (1.5 g, 4.85 mmol) was added bromo(2-methylpropyl)zinc (48.5 ml, 24.25 mmol) in tetrahydrofuran (50 ml) under argon. To the solution was then added 1,1' bis(diphenylphosphino)ferrocenedichloro palladium(II) dichloromethane complex (0.355 g, 0.485 mmol) and the reaction heated to reflux for 6 h. The mixture was 15 quenched with water (2 mL) and then filtered through celite, washing with ethyl acetate. The solvent was removed in vacuo. The residue was partitioned between ethyl acetate (50 mL) and water (50 mL) and the organic phase dried (phase separator) and the solvent removed in vacuo. The residue was purified by silica chromatography, eluting 0-15 % EtOAc in iso-hexane over 40 min. Two batches 20 were collected, one of which was the title compound as a colourless oil (233 mg, 1.072 mmol). 6H (CDC13, 400 MHz): 8.28 (1H, d), 8.15 (1H, dd), 7.38 (1H, d), 3.94, 3H, s), 2.78 (2H, d), 2.02 (1H, m), 0.96 (6H, d). 51 WO 2008/074821 PCT/EP2007/064185 Description for D32 3-Cyano-4-(2-methylpropyl)benzoic acid (D32) HO 0 N Methyl 3-cyano-4-(2-methylpropyl)benzoate (D31) (233 mg, 1.072 mmol) was 5 dissolved in ethanol (4 ml) and 2M aqueous sodium hydroxide (1 ml, 2 mmol) was added. The reaction was stirred for 1 h. 2M aqueous HCI (10 mL) was added and the mixture extracted with dichloromethane (20 mL + 10 mL). The organic phases were isolated and dried by phase separator and combined before the solvent was removed in vacuo to give the title compound as a white solid (203 mg, 0.999 mmol). 10 6H (d 6 -DMSO, 400 MHz) 13.43 (1H, br. s), 8.29 (1H, d), 8.14 (1H, dd), 7.59 (1H, d), 2.74 (2H, d), 1.96 (1 H, m), 0.91 (6H, d). MS (ES): C 12

H

13

NO

2 requires 203; found 202 (M-H*). Description for D33 15 4-(2-Methylpropyl)-3-(trifluoromethyl)benzamide (D33)

H

2 N 0

CF

3 To a solution of 4-bromo-3-trifluoromethylbenzonitrile (1.25 g, 5.0 mmol) and isobutylzinc bromide (25 mmol) in THF (50 mL, 25 mmol) under argon was added 1,1'-bis(diphenylphosphino)ferrocenedichloro palladium(II) dichloromethane complex 20 (612 mg, 0.75 mmol) and the reaction heated at reflux for 5 h. The mixture was concentrated in vacuo and the residue partitioned between ethyl acetate (80 mL) and water (80 mL). A solid formed and was filtered off and discarded. The organic layer was washed with water (80 mL) before it was dried (phase separator) and 52 WO 2008/074821 PCT/EP2007/064185 concentrated in vacuo to give the crude title compound as a black oil. This was used directly in the next step (1.35 g). Description for D34 5 4-(2-Methylpropyl)-3-(trifluoromethyl)benzoic acid (D34) HO 0

CF

3 4-(2-methylpropyl)-3-(trifluoromethyl)benzamide (D33) (1.35 g, 5.50 mmol) was dissolved along with potassium hydroxide (3.09 g, 55.0 mmol) in ethanol (40 ml) and water (10.0 ml) and the solution heated to reflux for 18 h. The reaction mixture was 10 concentrated in vacuo and the mixture separated between EtOAc (150 mL) and aqueous sodium hydroxide (2M, 150 mL). The layers were separated and the organic phase extracted with further sodium hydroxide solution (200 mL). LCMS of both phases showed product in both. Therefore the aqueous phase was acidified to pH1 with HCI (5M) and extracted back into EtOAc (2 x 150 mL) and these organic 15 phases combined with the original organic phase. The solvent was removed in vacuo and the residue purified by reverse phase chromatography, eluting 5-100 % MeCN in H 2 0 over 2000 mL and the solvent removed in vacuo to give a brown solid (690 mg, 2.410 mmol). This solid was triturated with hexane to give the title compound as a buff solid (135 mg, 0.548 mmol) and the filtrate purified by MDAP to 20 give further title compound as a white solid (102 mg, 0.414 mmol). 6H (d 6 -DMSO, 400 MHz): 13.39 (1H, br. s), 8.16 (1H, s), 8.13 (1H, d), 7.62 (1H, d), 2.69 (2H, d), 1.97 (1 H, m), 0.90 (6H, d). MS (ES): C 12

H

13

F

3 0 2 requires 246; found 245 (M-H*). Description for D35 25 5-Formyl-2-{[(1 S)-1 -methylpropyl]oxy}benzonitrile (D35) H O (0 NC 53 WO 2008/074821 PCT/EP2007/064185 (2S)-2-Butanol (0.99 g, 0.013 mol) was dissolved in DMF (50 ml) and the solution cooled to 0 0C. To this was added sodium hydride, (60% dispersion in mineral oil, 1.54g, 0.036 mol) in a portion-wise manner, the mixture was stirred at 0 0C for 10 minutes after complete addition. 2-Fluoro-5-formylbenzonitrile (2.0 g, 0.013 mol) was 5 then added and the reaction mixture allowed to warm to room temperature (slowly within the ice bath) and the reaction mixture was stirred overnight at room temperature. The reaction mixture was then cooled to 0 C, quenched with brine and diluted with EtOAc (-25ml). The mixture was partitioned and the organic fraction extracted with water (-30ml), the combined organics were dried by passing through 10 a phase separating cartridge and then evaporated to dryness under reduced pressure to give the crude product. The crude residue was purified on a 40+M Biotage cartridge, eluting with a 20 to 50 % mixture of EtOAc in hexane. This gave the title compound (220mg) as a white solid. 6H (d 6 -DMSO, 400 MHz): 9.88 (1H, s), 8.30 (1H, s), 8.15 (1H, d), 7.49 (1H, d), 4.73-4.81 (1H, m), 1.63-1.79 (2H, m), 1.33 15 (3H, d), 0.95 (3H, t). MS (ES): C 12

H

13

NO

2 requires 203; found 204 (MH*). Description for D36 3-Cyano-4-{[(1 S)-1 -methylpropyl]oxy}benzoic acid (D36) - OH O 0 I H (0 NC 20 To a solution of 5-formyl-2-{[(1 S)-1 -methylpropyl]oxy}benzonitrile (D35) (220mg, 1.08 mmol) in acetic acid (20ml) was added sodium perborate tetrahydrate (334mg, 2.17 mmol), the reaction mixture was heated at 50 0C over the weekend. The reaction mixture was concentrated in-vacuo. Water (-50ml) was added, EtOAc (-30ml) was added and the layers partitioned, the aq layer was extracted twice more with EtOAc 25 (-30ml) and the combined organics were evaporated to dryness under reduced pressure to give the title compound (245mg) as an off white solid. 6H (d 6 -DMSO, 400 MHz): 8.17 (2H, apparent d), 7.39 (1H, s), 4.68-4.74 (1H, m), 1.55-1.76 (2H, m), 1.31 (3H, d), 0.95 (3H, t). MS (ES): C 1 2

H

13

NO

2 requires 219; found 220 (MH*). 30 Description for D37 5-Formyl-2-{[(1 R)-1 -methylpropyl]oxy}benzonitrile (D37). 54 WO 2008/074821 PCT/EP2007/064185 lii... H NC (2R)-2-Butanol (0.99 g, 0.013 mol) was dissolved in DMF (50 ml) and the solution cooled to 0 0C. To this was added sodium hydride, 60% dispersion in mineral oil (1.54g, 0.036 mol) in a portion-wise manner, the mixture was stirred at 0 0C for 10 5 minutes after complete addition. 2-Fluoro-5-formylbenzonitrile (2.0 g, 0.013 mol) was then added and the reaction mixture allowed to warm to room temperature (slowly within the ice bath) and the reaction mixture was stirred overnight at room temperature. The reaction mixture was then cooled to 0 C, quenched with brine and diluted with EtOAc (-25ml). The mixture was partitioned and the organic fraction 10 extracted with water (-30ml), the combined organics were dried by passing through a phase separating cartridge and evaporated to dryness under reduced pressure to give the crude product. The crude residue was purified on a 40+M Biotage cartridge, eluting with a 20 to 50 % mixture of EtOAc in hexane. This gave the title compound (310mg) as a yellow oil. 6H (d 6 -DMSO, 400 MHz): 9.88 (1H, s), 8.30 (1H, s), 8.15 15 (1H, d), 7.49 (1H, d), 4.73-4.81 (1H, m), 1.63-1.79 (2H, m), 1.33 (3H, d), 0.95 (3H, t) ppm. Description for D38 3-Cyano-4-{[(1R)-1-methylpropyl]oxy}benzoic acid (D38) ""i - OH O 00 20 CN To a solution of 5-formyl-2-{[(1 R)- 1 -methylpropyl]oxy}benzon itrile (D37) (310mg, 1.53 mmol) in acetic acid (30ml) was added sodium perborate tetrahydrate (471mg, 3.05 mmol), the reaction mixture was heated at 50 0C over the weekend. The reaction mixture was concentrated in vacuo and water (-50ml) added, EtOAc (-30ml) was 25 added and the layers partitioned, the aq layer was extracted twice more with EtOAc (-30ml) and the combined organics evaporated to dryness under reduced pressure to give the title compound (315mg) as an off-white solid. 6H (d 6 -DMSO, 400 MHz): 8.07-8.24 (2H, m), 7.38 (1H, d), 4.63-4.77 (1H, m), 1.55-1.83 (2H, m), 1.31 (3H, d), 0.95 (3H, t). MS (ES*): C 12

H

13

NO

2 requires 219; found 220 (MH*). 55 WO 2008/074821 PCT/EP2007/064185 Description for D39 Methyl 6-(methyloxy)-3-bi phenylcarboxylate (D39) O 5 Methyl 3-bromo-4-(methyloxy)benzoate (245 mg, 1 mmol, commercially available) was dissolved in DME : 2N Na 2

CO

3 (2:1, 18 ml) and then phenyl boronic acid (244 mg) and tetrakistriphenylphosphine palladium(0) (58 mg) were added. The reaction was heated to 80 'C and then left to cool over the weekend. Added EtOAc and water, the organics were separated, dried and evaporated to give a black gum. 10 Purification by flash chromatography afforded the title compound (194 mg) as a gum. 6H (d 6 -DMSO, 400MHz) 3.83 (3H, s), 3.85 (3H, s), 7.24 (1H, d), 7.33-7.50 (5H, m), 7.83 (1 H, d), 7.97 (1 H, dd). MS (ES): C 15

H

1 4 0 3 requires 242; found 243 (MH*). Description for D40 15 6-(Methyloxy)-3-biphenylcarboxylic acid (D40) O OH Methyl 6-(methyloxy)-3-biphenylcarboxylate (D39) (194 mg, 0.8 mmol) dissolved in 2N NaOH aq. (3 ml) and methanol (3 ml). Stirred at room temperature overnight and then the organic solvent was evaporated in vacuo. Added EtOAc/water separated 20 and then acidified the aqueous and re-extracted. The organic extracts were dried and evaporated to afford 202 mg of the title compound as a white solid. 6H (d 6 -DMSO, 400MHz) 3.84 (3H, s), 7.22 (1H, d), 7.33-7.49 (5H, m), 7.82 (1H, d), 7.95 (1H, dd), MS (ES*): C 14

H

12 0 3 requires 228; found 229 (M+H*). 25 Description for D41 56 WO 2008/074821 PCT/EP2007/064185 3-Bromo-5-(5-{3-chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-y)-1 H indole (D41) Cl Br I- N N To 5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indole (D5) 5 (450mg, 1.27 mmol) dissolved in DMF (12ml) was added bromine (213mg, 1.35 mmol) dropwise. Stirred for 15 minutes, evaporated off the DMF, added diethyl ether (70ml) and washed with water (2x70ml). Dried over MgSO 4 and evaporated off the solvent. The residue was crystallised from diethyl ether/hexane to give 160mg of the title compound as a white solid. 6H (400 MHz, d 6 -DMSO) 1.37 (6H, d), 4.88 (1H, 10 sept), 7.44 (1H, d), 7.59 (1H, dd), 7.72 (1H, d), 7.91 (1H, dd), 8.13-8.32 (3H, m). MS (ES) C 1 9H 1 s 9 BrCIN 3 0 2 requires 431; found 432 (MH*). The following esters were prepared in a similar fashion to the previously described examples (such as D6) using the appropriate indole and alkylating agent. The alkyl 15 halides were commercially available apart from D11 used to prepare D48. Unless stated otherwise, the reactions were performed in DMF. On some occasions the reactions were worked up by an aqueous work-up procedure whilst on others the crude material was used directly in the hydrolysis step following evaporation of the reaction solvent. 20 Structure Name Precursor Comments MH+ indole D42 ethyl (5-{5-[4-phenyl- D2 solvent DMPU o'N 5-(trifluoromethyl)-2- rather than DMF. F N thienyl]-1,2,4- Reaction at 100 SO oxadiazol-3-yl}-1H- 120 0C in indol-1-yl)acetate microwave. 57 WO 2008/074821 PCT/EP2007/064185 D43 ethyl 3-[3-bromo-5- D41 Reaction 534 for HC CH, (5-{3-chloro-4-[(1- conventially 8Br methylethyl)oxy]phen heated to 80 *C 3CI yl}-1,2,4-oxadiazol-3 N Bryl)-1H-indol-1 , N yl]propanoate N D44 H C methyl 5-[5-(5-{3- D5 Reaction 468 CH3 Chloro-4-[(1- conventially 0 methylethyl)oxy]phen heated to 80 *C AI yl}-1,2,4-oxadiazol-3 C' yl)-1H-indol-1 yl]pentanoate 0 D45 ethyl 4-[5-(5-{3- D5 Reaction heated chloro-4-[(1- in the microwave HC methylethyl)oxy]phen at 130 0C. Crude yl}-1,2,4-oxadiazol-3- material used in yl)-1H-indol-1- next step yl]butanoate following evaporation. D46 methyl (2R)-3-[5-(5- D5 Reaction heated {3-chloro-4-[(1- in the microwave methylethyl)oxy]phen at 140 C. Crude yl}-1,2,4-oxadiazol-3- material used in yl)-1H-indol-1-yl]-2- next step methylpropanoate following evaporation. 58 WO 2008/074821 PCT/EP2007/064185 D47 | O-N ethyl (2S)-3-[5-(5-{3- D5 Reaction heated chloro-4-[(1- in the microwave N methylethyl)oxy]phen at 130 *C. Crude yl}-1,2,4-oxadiazol-3- material used in yl)-1H-indol-1-yl]-2- next step methyl propanoate following evaporation. D48 ethyl 2,2-dimethyl-3- D2 Reaction heated 540 (5-{5-[4-phenyl-5- in the microwave F \ O.. (trifluoromethyl)-2- at 131-150 *C. F N / thienyl]-1,2,4- Crude material F N oxadiazol-3-yl}-1 H- used in next step N CH3 indol-1-yl)propanoate following evaporation. Description for D49 5 5-[3-(1 H-indol-4-yl)-1,2,4-oxadiazol-5-yI]-2-[(1 -methylethyl)oxy]benzonitrile (D49) N 0 /0 N N N To 3-cyano-4-[(1-methylethyl)oxy]benzoic acid (can be prepared as described in W02005/58848) (500mg, 2.44 mmol) in DMF (15ml) was added EDAC (514mg, 2.67 59 WO 2008/074821 PCT/EP2007/064185 mmol) and HOBt (367 mg, 2.67 mmol) and the solution left standing for 30 minutes. Added N-hydroxy-1H-indole-4-carboximidamide (D9) (427 mg, 2.44 mmol) and left standing for 1 hour. To the solution were added EDAC (117mg, 0.61 mmol) and HOBt (84mg, 0.61 mmol) and left standing for 2 hours. To the solution were added 5 EDAC (234.9 mg, 1.22 mmol) and HOBt (167.7 mg, 1.22 mmol) and left standing overnight. Heated at 80 0C overnight, cooled and added EtOAc (30ml). Washed with water (30ml), sat. sodium hydrogen carbonate (30ml) and water (30ml). Dried over MgSO 4 and evaporated off the solvent. The residue was triturated with diethyl ether to give 353 mg of the title compound as a pale brown solid. 6H (400 MHz, d 6 -DMSO) 10 1.39 (6H, d), 4.94-5.03 (1H, m), 7.09-7.10 (1H, m), 7.30 (1H, t), 7.56-7.59 (2H, m), 7.67 (1H, d), 7.92 (1H, dd), 8.45 (1H, dd), 8.55 (1H, d), 11.52 (1H, broad s). MS (ES)

C

2 0

H

16

N

4 0 2 requires 344; found 345 (MH*). Description for D50 15 Ethyl 4-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yI)-1H indol-1 -yl]butanoate (D50) N /Y0 N N N EtO2C A mixture of 5-[3-(1 H-indol-4-yl)-1,2,4-oxadiazol-5-yl]-2-[( 1 methylethyl)oxy]benzonitrile (D49) (100mg, 0.29 mmol), ethyl 4-bromobutyrate (85 20 mg, 0.44mmol) and cesium carbonate (1 89mg, 0.58 mmol) in DMF (2ml) was heated at 80 0C for 1 hour. Added ethyl 4-bromobutyrate (85mg, 0.44 mmol) and heated overnight at 80 C. Added ethyl 4-bromobutyrate (85mg, 0.44 mmol) and cesium carbonate (189 mg, 0.58 mmol) and heated for 24 hours. Added ethyl 4 60 WO 2008/074821 PCT/EP2007/064185 bromobutyrate (85 mg, 0.44 mmol) and heated for 24 hours. Added ethyl 4 bromobutyrate (85mg, 0.44 mmol) and heated for 6 hours. Added EtOAc (20ml) and washed with water (20ml). Dried over MgSO 4 and evaporated off the solvent. The residue was crystallised from ethanol to give the title compound (55 mg) as a white 5 solid. MS (ES) C 2 6

H

26

N

4 0 4 requires 458; found 459 (MH*). Description 51 Ethyl 3-(5-cyano-1H-indol-1-yl)propanoate (D51) N

CO

2 Et 10 A mixture of 1H-indole-5-carbonitrile (1.42g, 10 mmol), ethyl 3-bromopropanoate (1.92ml, 15 mmol) and cesium carbonate (6.5g, 20 mmol) in DMF (50ml) was heated at 80 0C for 4 hours. Cooled the solution, added diethyl ether (300ml) and washed with water (3X 300ml). Dried over MgSO 4 and evaporated off the solvent to yield 2.4g of pale orange oil. This crude product was used in the next stage (preparation of 15 D52). Description for D52 Ethyl 3-{5-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate HO, H2N

H

2 N N

CO

2 Et 20 Ethyl 3-(5-cyano-1H-indol-1-yl)propanoate (D51) (1.7g, 7.2 mmol), hydroxylamine hydrochloride (1.0g, 14.4 mmol) and sodium hydrogen carbonate (2.42g, 28.9 mmol) were suspended in ethanol (100ml) and stirred at 50 0C for 3 days. A single product formed but 15% starting material remained. Cooled, filtered off the inorganic material and evaporated off the solvent. The product was crystallised from a mixture of 61 WO 2008/074821 PCT/EP2007/064185 EtOAc, diethyl ether and hexane to yield 1.9g of the title compound as a white solid. MS (ES) C 14

H

17

N

3 0 3 requires 275; found 276. (MH*). Description for D53 5 Ethyl 3-[5-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yI)-lH indol-1 -yl]propanoate (D53) N ~N O N N

CO

2 Et 10 3-Cyano-4-[(1-methylethyl)oxy]benzoic acid (can be prepared as described in W02005/58848) (215mg, 1.05 mmol), EDAC (219mg, 1.14 mmol) and HOBt (156mg, 1.14 mmol) in dry DMF (10ml) were stirred at RT for 10 minutes. Added ethyl 3-{5-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D52) (288mg, 15 1.05 mmol) and stirred for 1 hour at RT. Heated at 80 0C for 7 hours. The solution was cooled and EtOAc (50ml) added. Washed with water (50ml), sat. sodium hydrogen carbonate (50ml) and water (50ml). Dried over MgSO 4 and evaporated off the solvent. The residue was crystallised from ether to yield 200mg of the title compound as a very pale pink solid. MS (ES) C2 5

H

24

N

4 0 4 requires 444; found 445 20 (MH*) Description for D54 Ethyl 3-(4-cyano-1H-indol-1-yl)propanoate (D54) CN N / 62 WO 2008/074821 PCT/EP2007/064185 4-Cyanoindole (2.5 g) was dissolved in DMF (7.5 ml). Cs 2

CO

3 (11.46 g) was added followed by ethyl 3-bromopropionate (3.38 ml). This mixture was heated to 80 'C for 40 minutes. A further portion of DMF (5 ml) was added and heating at 80 'C continued for 1 hour. The reaction mixture was evaporated then dissolved in H 2 0 5 (200 ml) and extracted with EtOAc (200 ml). This was evaporated to give a yellow oil (3.5 g) which was purified on a 40+M Biotage cartridge, eluting with a 25-75 % mixture of Et 2 0 in hexane. This gave the title compound (3.44 g) as a pale yellow oil. 6H (CDC13, 400MHz): 1.19 (3H, t), 2.82 (2H, t), 4.12 (2H, q), 4.50 (2H, t), 6.71 (1H, d), 7.23-7.28 (1H, m), 7.33 (1H, d), 7.47 (1H, d), 7.60 (1H, dd). MS (ES): C 1 4

H

14

N

2 0 2 10 requires 242; found 243 (MH*). The following example was prepared by a similar method to those described above. The reaction was not complete after the work-up and so the material was resubmitted to the reaction conditions with an extra 0.2 equivalents of base and 15 alkylating agent and the product was purified by trituration with ether. Number Structure Name MH* D55 CN ethyl (4-cyano-1H- 229 indol-1-yl)acetate N 0 CH, Description for D56 Ethyl 4-(4-cyano-1 H-indol-1 -yl)butanoate (D56) 63 WO 2008/074821 PCT/EP2007/064185 CN NN

H

3 C 01 0 Combined 4-cyanoindole (5 g, 35.2 mmol), ethyl-4-bromobutanoate (10.29 g, 52.8 mmol) and cesium carbonate (22.92 g, 70.3 mmol) and heated to 80 'C under argon for 1 hour. The reaction was allowed to cool and then 150ml diethyl ether was added 5 and the organic solution was washed with 3 x 150ml H 2 0. Dried the organic solution over MgSO 4 and evaporated the solvent. Dried on high vacuum over the weekend to afford the title compound (8.25 g) as an orange oil. 6H (400 MHz, d 6 -DMSO). 1.13 (3H, t), 1.96-2.05 (2H, m), 2.26 (2H, t), 3.99 (2H, q), 4.29 (2H, t), 6.60 (1H, dd), 7.29 (1H, apparent t), 7.55 (1H, dd), 7.68 (1H, d), 7.90 (1H, d). MS (ES): C 15

H

1 6

N

2 0 2 10 requires 256; found 257 (MH*). Description for D57 Ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1 H-indol-1 -yl}propanoate (D57) OH

H

2 N ,-N N \ 0 15 Ethyl 3-(4-cyano-1H-indol-1-yl)propanoate (D54) (3.44 g), NH 2 OH.HCI (1.97 g) and Na 2

CO

3 (5.96 g) were dissolved in EtOH (75 ml). This mixture was heated at 50 'C overnight. A further portion of NH 2 OH.HCI (985 mg) was added and the mixture stirred at 70 'C overnight. The reaction mixture was then filtered and evaporated to give the title compound (4.06 g). MS (ES): C 14

H

17

N

3 0 3 requires 275; found 276 (MH*) 20 64 WO 2008/074821 PCT/EP2007/064185 Description for D57 (alternative procedure) Ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1 H-indol-1 -yl}propanoate (D57) OH

H

2 N ,-N N \ 0 A mixture of 1 H-indole-4-carbonitrile (3.4 g, 23.92 mmol), ethyl 3-bromopropanoate 5 (4.57 ml, 35.9 mmol) and cesium carbonate (15.59 g, 47.8 mmol) was heated at 80 'C for 2 hours and left standing overnight. Ether (400ml) was added and the resulting mixture was washed with water (3X400ml), dried over MgSO 4 and evaporated to yield 6.6 g of pale yellow clear oil The oil N4111-30-A2 (6.6 g, 27.2 mmol), hydroxylamine hydrochloride (3.79 g, 54.5 10 mmol) and sodium bicarbonate (9.15 g, 109 mmol) in ethanol were stirred at 50 0C overnight. Added further hydroxylamine hydrochloride (2.3g) and heated at 50 0C for 24 hours. The reaction was filtered the residue washed with DCM (50ml). The solvent was removed by evaporation and the residue triturated with hexane to obtain the title compound (4.2g) as a white solid. Further title compound (1.0 g) as a white 15 solid was obtained from trituration of residues. Mass spectral data consistent with previous synthesis. The following was made in a similar fashion to the first D57 procedure listed, sodium bicarbonate was the base used and the reaction was carried out at 55 0C. 20 Number Structure precursor Name MH* number D58 OH D55 ethyl {4- 262 [(hydroxyami N NH 2 no)(irnino)rnet hyl]-1H-indol 1-yl}acetate N 0 CH3 65 WO 2008/074821 PCT/EP2007/064185 Description for D59 Ethyl 4-{4-[(hydroxyamino)(imino)methyl]-1 H-indol-1 -yl}butanoate (D59) OH N NH 2 N

H

3 C 01 0 Ethyl 4-(4-cyano-1H-indol-1-yl)butanoate (D56) (8.25 g, 32.2 mmol) was dissolved in 5 EtOH and treated with NH 2 OH.HCI (4.47 g, 64.4 mmol) and NaHCO 3 (8.11 g, 97 mmol) and heated to 550C for 1 day and two nights. Further NH 2 OH.HCI (500 mg) and NaHCO 3 (500 mg) were added and the reaction was heated for another 3 hours and then separated the inorganics by filtration, washing well with EtOH. The solvent was evaporated and the residue dried under high vacuum. Trituration with ether and 10 dcm afforded two batches of the title compound N2668-20-A8 (5.14 g) and N2668 20-A9 (976 mg). 6H (400 MHz, d 6 -DMSO) 1.15 (3H, t), 1.98 (2H, apparent quin), 2.25 (2H, t), 4.03 (2H, q), 4.21 (2H, t), 5.73 (2H, br s), 6.82 (1H, dd), 7.15 (1H, apparent t), 7.27 (1H, dd), 7.35 (1H, d), 7.51 (1H, d), 9.58 (1H, br s). MS (ES): C 15

H

1 9

N

3 0 3 requires 289; found 290 (MH*). 15 Description for D60 1-Methylethyl 5-chloro-6-[(1 -methylethyl)oxy]-3-pyridi necarboxylate (D60) 0 N~ CI 0 0 66 WO 2008/074821 PCT/EP2007/064185 The 5-chloro-6-hydroxy-3-pyridinecarboxylic acid (1g, 5.76 mmol) was suspended in toluene (200ml) and treated with silver carbonate (3.97 g, 14.40 mmol) and 2 iodopropane (3.46 ml, 34.6 mmol) and stirred at RT in the dark for 3 days. LC/MS showed 2/3 product. Added 2-iodopropane (3ml) and stirred for 24 hours. LC/MS 5 showed 80% product. Added EtOAc (200ml) and washed with water (200ml) + sat. NaHCO 3 (50ml) followed by water (200ml). Dried over MgSO 4 and evaporated off the solvent to yield 1.0g of the title compound as a clear, colourless oil. MS (ES*)

C

12

H

1 6 35 CIN0 3 requires 257; found 257. 10 Description for D61 5-Chloro-6-[(1-methylethyl)oxy]-3-pyridinecarboxylic acid (D61) O N C 0 OH 1-methylethyl 5-chloro-6-[(1 -methylethyl)oxy]-3-pyridinecarboxylate (D60) (1.6 g, 15 6.21 mmol) in isopropanol (70 ml) and water (35.0 ml) was treated with 2N sodium hydroxide (6.21 ml, 12.42 mmol) and stirred for 3 hours to give a single product. Evaporated off the IPA, acidified with glacial acetic acid and extracted product into EtOAc (100ml). Dried over MgSO 4 and evaporated off the solvent to yield 1.30 g of the title compound as a white solid. MS (ES) C 9

H

1 0 35 CIN0 3 requires 215; found 214 20 (M-H*). 25 67 WO 2008/074821 PCT/EP2007/064185 Description for D62 Ethyl 3-[4-(5-{5-chloro-6-[(1 -methylethyl)oxy] -3-pyridi nyl}-1,2,4-oxadiazol -3-yl) 1 H-indol-1 -yl]propanoate (D62) 0 Cl N\ / / 0 N ZN N 0 0 5 To 5-chloro-6-[(1-methylethyl)oxy]-3-pyridinecarboxylic acid (D61) (1.504 g, 6.97 mmol) in dry DMF (30ml) was added EDC (1.604 g, 8.37 mmol) and HOBT (1.282 g, 8.37 mmol). Stirred solution at RT for 10 minutes then added ethyl 3-{4 [(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (N4111-31-A4) (D57) (1.92 g, 6.97 mmol). The mixture was stirred for 30 minutes. LC/MS showed one product 10 (intermediate). The solution was heated at 80 0C for 2 hours. Left standing overnight at RT then heated 80 0C for further 2 hours to give complete reaction. Cooled and added EtOAc (250ml). The EtOAc was washed with sat. NaHCO 3 (150ml) followed by water (2X 200ml). Dried over MgSO 4 and evaporated off the solvent. The residue was subjected to chromatography on the biotage (EtOAc/hexane 1:2). On 15 evaporation of most of the solvent from clean fractions and addition of hexane a white precipitate was formed. The solid was filtered off to obtain 1.1 g of the title product. MS (ES) C 23

H

23 35

CIN

4 0 4 requires 454; found 455 (MH*). 20 68 WO 2008/074821 PCT/EP2007/064185 Description for D63 Ethyl 3-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yI)-lH indol-1 -yl]propanoate (D63) N 0 /0 N N N 5

CO

2 Et The 3-cyano-4-[(1-methylethyl)oxy]benzoic acid (can be prepared as described in W02005/58848) (113mg, 0.55mmol), EDAC (115mg, 0.60 mmol) and HOBt (82mg, 0.60 mmol) were dissolved in DMF (5ml) and left standing for 15 minutes. Added ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D57) (150mg, 10 0.55 mmol) and stood overnight at RT. Heated solution at 80 0C for 2 hours. LC/MS showed mostly product. After heating for a few more hours there was no change. Added EtOAc (20ml) and washed with water (30ml). Washed with saturated sodium hydrogen carbonate (30ml) and water (2X 30ml). Dried over MgSO 4 and evaporated off the solvent to obtain 81 mg of the title compound as a pale brown solid. MS (ES) 15 C 25 H44N 4 0 4 requires 444; found 445 (MH*). 20 69 WO 2008/074821 PCT/EP2007/064185 Description for D64 Ethyl 3-(4-{5-[2-(trifluoromethyl)-4-biphenylyl]-1,2,4-oxadiazol-3-y}-1H-indol-1 yl)propanoate (D64) F F F / 0 N N N

CO

2 Et 5 To 2-(trifluoromethyl)-4-biphenylcarboxylic acid (D29) (146mg, 0.55mmol) in DMF (5ml) was added EDC (115mg, 0.60 mmol) and HOBt (82mg, 0.60 mmol) and the solution left standing for 15 minutes. Added ethyl 3-{4 [(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D57) (150mg, 0.55 mmol) and stirred at RT for 1 hour. Heated at 80 0C for 1 hour then heated overnight. 10 Cooled then added EtOAc (20ml). Washed with water (20ml), sat aqueous sodium hydrogen carbonate (20ml) and water (20ml). Dried over MgSO 4 then evaporated of the solvent. The residue was triturated with ethanol to give 157 mg of the title compound as a white solid. 6H (400 MHz, d 6 -DMSO) 1.11 (3H, t), 2.90 (2H, t), 4.02 (2H, q), 4.55 (2H, t), 7.10 (1H, d), 7.32-7.48 (3H, m), 7.49-7.61 (3H, m), 7.61 (1H, d), 15 7.73-7.84 (2H, m), 8.00 (1H, d), 8.53-8.56 (2H, m). MS (ES) C 28

H

22

F

3

N

3 0 3 requires 505; found 506 (MH*). 20 70 WO 2008/074821 PCT/EP2007/064185 Description for D65 (alternative to description for D50) Ethyl 4-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-lH indol-1 -yl]butanoate (D65) 0 N /0 N N N 0 0 5 A mixture of 3-cyano-4-[(1-methylethyl)oxy]benzoic acid (can be prepared as described in W02005/58848) (1.21g, 5.88 mmol), EDC (1.35g, 7.05 mmol) and HOBt (1.08g, 7.05 mmol) in dry DMF (85 ml) was stirred for 20 minutes at RT. Added ethyl 4-{4-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}butanoate (D59) (1.70g, 5.88 mmol) and stirred at RT for 1 hour. Heated mixture at 80 0C for 5 hours and left 10 overnight at RT. Heated at 80 0C for 6 hours then evaporated off the DMF. Added EtOAc (200ml) and washed with sat. NaHCO 3 (200ml) and water (200ml). Dried over MgSO 4 and evaporated off the solvent. Subjected the residue to chromatography using the biotage (EtOAc/hexane 1:2) and evaporated the cleanest fractions to yield 1.42g the title compound as a white solid. 6H (400 MHz, d 6 -DMSO) 1.15 (3H, t), 1.39 15 (6H, d), 2.04 (2H, apparent quintet), 2.24 (2H, t), 4.00 (2H, q), 4.31 (2H, t), 4.94-5.04 (1H, m), 7.10 (1H, dd), 7.31 (1H, t), 7.56-7.60 (2H, m), 7.77 (1H, d), 7.95 (1H, d), 8.45 (1 H, dd), 8.56 (1 H, d). MS (ES) C2 6

H

26

N

4 0 4 requires 458; found 459 (MH*). 20 71 WO 2008/074821 PCT/EP2007/064185 Description for D66 4-(1 -Cyclohexen-1 -yI)-3-(trifluoromethyl)benzamide (D66) 0 H2N

CF

3 5 4-bromo-3-(trifluoromethyl)benzonitrile (commercial) (1.2 g, 4.80 mmol), 1 cyclohexen-1-ylboronic acid (0.907 g, 7.20 mmol), sodium methoxide (0.778 g, 14.40 mmol) and bis(triphenylphosphine)palladium(II) chloride (0.337 g, 0.480 mmol) were added to dry methanol (12 mL) and the mixture heated in the microwave at 80 'C for 10 10 minutes. The reaction mixture was partitioned between ethyl acetate (40 mL) and water (40 mL) and then the organic phase washed with further water (40 mL). The organic phase was dried (MgSO 4 ), filtered and the solvent removed in vacuo. The crude product was purified by flash silica chromatography, eluting with 0-75 % ethyl acetate in hexane to give the title compound as a white solid (1.02 g). 6H (CDC13, 15 400 MHz): 8.09 (1H, m), 7.90 (1H, dd), 7.32 (1H, d), 6.3-5.8 (2H, m) 5.61 (1H, s), 2.25-2.13 (4H, m), 1.80-1.60 (4H, m). MS (ES): C 14

H

14

F

3 NO requires 269; found 270 (MH*). Description for D67 20 GSK1929583A, N2123-11-A2 4-Cyclohexyl-3-(trifluoromethyl)benzamide (D67) 0 H 2 N

CF

3 4-(1-Cyclohexen-1-yl)-3-(trifluoromethyl)benzamide (D66) (850 mg, 3.16 mmol) was 25 dissolved in methanol (63 ml) and hydrogenated using an H-Cube, using palladium on carbon at 40 0C with a flow rate of 2 mL/min. The solvent was removed in vacuo to give the title compound as a white solid (822 mg). 6H (CDC13, 400 MHz): 8.08 (1 H, d), 7.94 (1H, dd), 7.52 (1H, d), 6.54 (2H, brs), 2.97 (1H, m), 1.90-1.75 (5H, m), 1.50 1.22 (5H, m). MS (ES): C 1 4

H

16

F

3 NO requires 271; found 272 (MH*). 72 WO 2008/074821 PCT/EP2007/064185 Description for D68 4-Cyclohexyl-3-(trifluoromethyl)benzoic acid (D68) 0 _ HO 5

CF

3 To a solution of 4-cyclohexyl-3-(trifluoromethyl)benzamide (D67) (822 mg, 3.03 mmol) in ethanol (40 ml) was added potassium hydroxide (1.700 g, 30.3 mmol) and water (5 ml) and the reaction heated to 90 0C block temperature for 3 h and stirred at 10 room temperature for 16 h. Further potassium hydroxide (1.700 g, 30.3 mmol) was added and the reaction heated at reflux for 27 h. A further 5 mL of water was added and the reaction heated for 66 hours (weekend). The reaction mixture was concentrated in vacuo and the residue partitioned between ethyl acetate (25 mL) and aqueous hydrochloric acid (2M, 25 mL). The aqueous layer was further extracted 15 with ethyl acetate (25 mL) and the combined organic phases dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound as a white solid (737 mg). 6H (methanol-d 4 , 400 MHz): 8.24 (1H, d), 8.18 (1H, dd), 7.68 (1H, d), 2.98 (1H, t), 1.72-1.95 (5H, m), 1.30-1.58 (5H, m). MS (ES): C 14

H

15

F

3 0 2 requires 272; found 271 (M-H*). 20 Description for D69 Ethyl 3-(4-{5-[4-cyclohexyl-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-lH indol-1 -yl)propanoate (D69) /

CF

3 0 1 \ N, N N 0 0 73 WO 2008/074821 PCT/EP2007/064185 A solution of 4-cyclohexyl-3-(trifluoromethyl)benzoic acid (D68) (148 mg, 0.545 mmol), EDC (115 mg, 0.599 mmol) and HOBt (92 mg, 0.599 mmol) in DMF (5 ml) was stirred for 10 min before addition of ethyl 3-{4-[((hydroxyamino)(imino)methyl] 1H-indol-1-yl}propanoate (D57) (150 mg, 0.545 mmol). The reaction was stirred for 5 30 min at room temperature followed by 16 h at 80 0C. The reaction mixture was partitioned between ethyl acetate (25 mL) and water (25 mL) and the organic phase washed with aqueous sodium bicarbonate (25 mL) and then water (25 mL). The organic phase was dried (phase separator) and the solvent removed in vacuo. The crude product was purified by MDAP. Some of the mixture submitted for MDAP had 10 precipitated and was triturated with ethanol and filtered. The white solids were combined to give the title compound (63 mg). MS (ES): C 28

H

2 8

F

3

N

3 0 3 requires 511; found 512 (MH*). Description for D70 15 1-Methylethyl 4-[(1-methylethyl)oxy]-3-(trifluoromethyl)benzoate (D70) 0 / ~ CF 3 0== 0 A mixture of 4-hydroxy-3-(trifluoromethyl)benzoic acid (commercial) (450 mg, 2.18 20 mmol), 2-iodopropane (435 pL, 4.36 mmol) and potassium carbonate (603 mg, 4.36 mmol) in N,N'-dimethylformamide (40 mL) was heated at 70 'C for 4 h before further 2-iodopropane (218 pL, 2.18 mmol) was added and the heating continued for 18 h. The inorganic solid was filtered off and rinsed with ethyl acetate. The filtrate was concentrated in vacuo and partitioned between ethyl acetate (150 mL) and water 25 (150 mL) containing some aqueous sodium hydroxide. The organic layer was dried (phase separator) and concentrated in vacuo to give the crude title compound (704 mg) as a yellow oil. MS (ES): C 14

H

17

F

3 0 3 requires 290; found 291 (MH*). 74 WO 2008/074821 PCT/EP2007/064185 Description for D71 4-[(1-Methylethyl)oxy]-3-(trifluoromethyl)benzoic acid (D71) 0

CF

3 0 OH 5 To a mixture of 1-methylethyl 4-[(1 -methylethyl)oxy]-3-(trifluoromethyl)benzoate (D70) (704 mg, 2.43 mmol) in ethanol (110 mL) was added aqueous sodium hydroxide (2M, 12.2 mL, 24.3 mmol) and the reaction heated to reflux for 1 h. The mixture was concentrated in vacuo and the residue partitioned between ethyl acetate 10 (100 mL) and water (100 mL) and acidified with aqueous hydrochloric acid (2M, 13 mL). The aqueous layer was extracted further with ethyl acetate (100 mL) and the combined organic layers dried and concentrated in vacuo to give the title compound as a yellow solid (563 mg). 6H (methanol-d 4 , 400 MHz): 8.21-8.17 (2H, m), 7.26 (1H, d), 4.84 (1H, septet), 1.38 (6H, d). MS (ES): C 1 1

H

11

F

3 0 3 requires 248; found 247 (M 15 H*). Description for D72 Ethyl 3-(4-{5-[4-[(1-methylethyl)oxy]-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol 3-yl}-1 H-indol-1 -yl)propanoate (D72) 0 I CF 3 0 I \ N N N 0 20 75 WO 2008/074821 PCT/EP2007/064185 4-[(1-Methylethyl)oxy]-3-(trifluoromethyl)benzoic acid (D71) (136 mg, 0.55 mmol), EDC (116 mg, 0.61 mmol) and HOBt (82 mg, 0.61 mmol) were stirred in N,N dimethylformamide (5 mL) for 20 min. Ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1H 5 indol-1-yl}propanoate (D57) (150 mg, 0.55 mmol) was added and the reaction stirred at room temperature for 3 h and then 80 'C for 18 h. The reaction mixture was partitioned between ethyl acetate (25 mL) and water (25 mL). The organic layer was washed with aqueous sodium bicarbonate (25 mL) and water (25 mL) before it was dried (phase separator), filtered and concentrated in vacuo. The residue was 10 triturated with ethanol to give the title compound (85 mg). 6H (d 6 -DMSO, 400 MHz): 8.44 (1H, dd), 8.35 (1H, d), 7.95 (1H, d), 7.81 (1H, d), 7.62-7.58 (2H, m), 7.36 (1H,app. t), 7.07 (1H, d), 4.99 (1H, septet), 4.54 (2H, t), 4.02 (2H, q), 2.89 (2H, t), 1.36 (6H, d), 1.11 (3H, t). MS (ES*): C 2 5

H

24

F

3

N

3 0 4 requires 487; found 488 (MH*). 15 The following examples were prepared in a similar fashion to those described above. On occasion additional EDAC was required (up to 2.6 equiv) and in the case of D80 it was necessary to elevate the temperature to 120 'C. Workup was either aqueous or alternatively the solvent was removed in vacuo. In the case of D92 ethanol was added to the reaction mixture and the resultant precipitate was filtered. The 20 compounds were purified either by trituration, MDAP, normal or reversed phase chromatography. Structure Precursors Name MH* D73 CH3 D58 & D4 ethyl [4-(5-{3-chloro-4-[(1- 440/ Ci O methylethyl)oxy]phenyl}- 442 CH 1,2,4-oxadiazol-3-yl)-1 H

/H

3 indol-1-yl]acetate 0 I \ N N N 0 76 WO 2008/074821 PCT/EP2007/064185 D74 N D58 ethyl [4-(5-{3-cyano-4-[(1- 431

\CH

3 methylethyl)oxy]phenyl} \ 1,2,4-oxadiazol-3-yl)-1 H \ CH 3 indol-1-yl]acetate 0 / \ N N N D75 N D59 ethyl 4-[4-(5-{3-cyano-4- 459 \ H0 CH, methylethyl)oxy]phenyl} 1,2,4-oxadiazol-3-yl)-1 H indol-1-yl]butanoate 0 N N 0 D76 F D57 & D30 ethyl 3-(4-{5-[2'-fluoro-2- 524 F F (trifluoromethyl)-4 F biphenylyl]-1,2,4 oxadiazol-3-yl}-1 H-indol 1-yl)propanoate 0 / \ N \-7 77 WO 2008/074821 PCT/EP2007/064185 D77 CH 3 D59 & D4 ethyl 4-[4-(5-{3-chloro-4- 468 C0 CH 3 methylethyl)oxy]phenyl} 1,2,4-oxadiazol-3-yl)-1 H 0 indol-1-yl]butanoate N \-K 0 D78 F D59 ethyl 4-[4-(5-{3-chloro-4- 494 CI O-( F [(trifluoromethyl)oxy]phen F yl-1,2,4-oxadiazol-3-yl) 1H-indol-1-yl]butanoate 0 N 0 D79 CH, D59 & D61 ethyl 4-[4-(5-{5-chloro-6- 469 ci o [(1-methylethyl)oxy]-3 N CH 3 pyridinyl}-1,2,4-oxadiazol 3-yl)-lH-indol-1 0 yl]butanoate N 0 78 WO 2008/074821 PCT/EP2007/064185 D80 F D59 ethyl 4-(4-{5-[4-phenyl-5- 526 F F (trifluoromethyl)-2 thienyl]-1,2,4-oxadiazol-3 s yl}-1H-indol-1 yl)butanoate 0 N \-'\ 0 D81 D59 & D29 ethyl 4-(4-{5-[2- 520 F F (trifluoromethyl)-4 F biphenylyl]-1,2,4 oxadiazol-3-yl}-1 H-indol 1-yl)butanoate 0 \,\ N 0 D82 D57 ethyl 3-(4-{5-[4- 460 (methyloxy)-3 (trifluoromethyl)phenyl] F F 1,2,4-oxadiazol-3-yl}-1 H HC O indol-1 -yl)propanoate N O 79 WO 2008/074821 PCT/EP2007/064185 D83 N H D59 & D38 ethyl 4-{4-[5-(3-cyano-4- 473 \

{[(,R)-C

CH3 methyl propyl]oxy}phenyl) 1,2,4-oxadiazol-3-yl]-1 H indol-1-yl}butanoate N D84 N D59 & D36 ethyl 4-{4-[5-(3-cyano-4- 473 \ H[(IS)- / VCH 3 methylpropyl]oxy}phenyl) 1,2,4-oxadiazol-3-yl]-1 H indol-1-yl}butanoate 0 N 0 D85 D57 & D13 ethyl 3-(4-{5-[3-ethyl-4-(1- 473 piperidinyl)phenyl]-1,2,4 oxadiazol-3-yl}-1 H-indol 1-yl)propanoate D86 D57 & D19 ethyl 3-{4-[5-(4- 472 'N\_8 o-\ cyclohexyl-3 ethylphenyl)-1,2,4 oxadiazol-3-yl]-1 H-indol 1-yl}propanoate 80 WO 2008/074821 PCT/EP2007/064185 D87 D57 & D15 ethyl 3-(4-{5-[5-chloro-6- 466 (1-pyrrolidinyl)-3 pyridinyl]-1, 2,4-oxadiazol 3-yl}-1H-indol-1 yl)propanoate D88 D59 & D21 ethyl 4-[4-(5-{3-bromo-4- 512 [(1 0 methylethyl)oxy]phenyl} H B 1,2,4-oxadiazol-3-yl)-1 H indol-1-yl]butanoate D89 D59 & D24 ethyl 4-(4-{5-[3-chloro-4- 466 N N(2-methylpropyl)phenyl] CH / N1O,2,4-oxadiazol-3-yl}-1 H HC indol-1-yl)butanoate Cl D90 CH, D57 & D34 ethyl 3-(4-{5-[4-(2- 486 CH, methylpropyl)-3 F (trifluoromethyl)phenyl] F 1,2,4-oxadiazol-3-yl}-1 H - F indol-1 -yl)propanoate / \ N 8N 00 81 WO 2008/074821 PCT/EP2007/064185 D91 CH, D59 & D32 ethyl 4-(4-{5-[3-cyano-4- 457 (2-methylpropyl)phenyl] CH/ 1,2,4-oxadiazol-3-yl}-1 H -N indol-1-yl)butanoate N 0 D92 D59 & D27 ethyl 4-{4-[5-(2-cyano-4- 477 biphenylyl)-1,2,4 oxadiazol-3-yl]-1 H-indol 1-yl}butanoate 0 NN N 0 Description for D93 3-Chloro-4-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yI}-lH indole (D93) CI O-N NH N F S F 5 F This material was prepared in a similar fashion to D7 (CQ107723-108A2) from D10 except that the reaction was stirred for four hours rather than overnight. MS (ES):

C

21

H

11

CIF

3

N

3 0S requires 445; found 446 (MH*). 10 82 WO 2008/074821 PCT/EP2007/064185 Description for D94 3-Chloro-1H-indole-5-carbonitrile (D94) CI N 5 To a solution of 5-cyanoindole (3.0g, 21mmol) in dry DMF (50ml) was added N chlorosuccinimide (2.94g, 22 mmol) and the solution stirred at room temperature for 1 hour. The solution was left standing over the weekend. LC/MS showed a single product. Added ethyl acetate (150ml) and diethyl ether (50ml) and washed with water 10 (3X 300ml). Dried over MgSO 4 and evaporated off the solvent to yield 3.9 g of the title compound as a pale yellow solid. 6H (400 MHz, d 6 -DMSO) 7.54 (1H, dd), 7.61 (1H, dd), 7.78 (1H, d), 8.01-8.02 (1H, m), 12.2 (1H, broad s). MS (from LCMS of reaction mixture) (ES):C9H 5

CIN

2 requires 176; found 177 (MH*). 15 Description for D95 Ethyl 3-(3-chloro-5-cyano-1H-indol-1-yl)propanoate (D95) N Cl N

CO

2 Et A mixture of 3-chloro-1H-indole-5-carbonitrile (D94) (1.8g, 10mmol), ethyl-3 bromopropionate (1.92ml, 15mmol), cesium carbonate (6.5g, 20mmol) and DMF 20 (50ml) was heated at 80 0C for 4 hours to give complete reaction. After allowing mixture to cool to room temperature diethyl ether (300ml) was added and the solution washed with water (3X300ml). Dried over MgSO 4 and evaporated off the solvent to give a brown solid. The solid was triturated with a mixture of diethyl ether and hexane to obtain 2.5g of the title compound as a tan solid. Crude product used 25 in the next stage (synthesis of D96). 83 WO 2008/074821 PCT/EP2007/064185 Description for D96 Ethyl 3-{3-chloro-5-(hydroxyamino)(imino)methyl]-1 H-indol-1 -yl}propanoate (D96) 5 HON c

H

2 N N

CO

2 Et 10 A mixture of ethyl 3-(3-chloro-5-cyano-1H-indol-1-yl)propanoate (D95) (2.0g, 7.2 mmol), hydroxylamine hydrochloride (1.0g, 14.4 mmol), sodium hydrogen carbonate (2.42g, 28.9 mmol) and ethanol (100ml) was heated at 50 0C over the weekend. Still 25% starting material present by LC/MS. Added hydroxylamine hydrochloride (0.5g, 7.2 mmol) and sodium hydrogen carbonate (1.2g, 14.3 mmol) and heated at 50 0C 15 for 24 hours. There was only a small amount of starting material present so it was decided to work up the reaction. The inorganic material was filtered off. The solvent was evaporated and the residue triturated using ethyl acetate and diethyl ether to yield 1.9 g of the title compound as a pale yellow solid. MS (ES) C 1 4

H

1 6

CIN

3 0 3 requires 309; found 310 (MH*). 20 Description for D97 Ethyl 3-[3-chloro-5-(5-{3-chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4-oxadiazol 3-yl)-1 H-indol-1 -yl]propanoate (D97) F CI c1 F~O N 25 CO2Et 84 WO 2008/074821 PCT/EP2007/064185 3-Chloro-4-[(trifluoromethyl)oxy]benzoic acid (commercial: ABCR) (168mg, 0.70 mmol) stirring in DMF (6ml) was treated with EDC (146mg, 0.76 mmol) followed by 5 HOBt (104mg, 0.76 mmol). The resultant solution was stirred for 15 minutes. Added ethyl 3-{3-chloro-5-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D96) (216mg, 0.70 mmol) and stirred at RT for 45 minutes. The solution was heated at 80 0C for 6 hours then left standing at room temperature overnight. Single product formed by LC/MS. Added EtOAc (50ml) and washed with water (50ml), saturated 10 aqueous sodium hydrogen carbonate (50ml) and water (50ml). Dried over MgSO 4 and evaporated off the solvent. The residue was crystallised from ethanol to yield 200mg of white solid. 6H (400 MHz, d 6 -DMSO) 1.11 (3H, t), 2.92 (2H, t), 4.00 (2H, q), 4.49 (2H, t), 7.75 (1H, s), 7.80 (1H, d), 7.85 (1H, dd), 7.95 (1H, dd) 8.23 (1H, d) 8.30 (1H, dd), 8.47 (1H, d). MS (ES) C 22

H

16 35

CI

37

CIF

3

N

3 0 4 requires 515; found 516 15 (MH*). Description for D98 (alternative to description for D28) Ethyl 4-chloro-3-(trifluoromethyl)benzoate (D98) Cl F 20 F A solution of 4-chloro-3-trifluoromethyl benzoic acid (10 g, 44.5 mmol) in ethanol (10 ml) was split equally between two microwave vials. Concentrated sulfuric acid (0.75 ml) was added to each vial (1.5 ml in total). The reactions were heated in the microwave at 120 'C for 30 minutes in total. The reaction mixtures were combined 25 and concentrated in vacuo. The residue was partitioned between EtOAc (100 ml) and aq. sodium bicarbonate (100 ml), the organic phase was separated, washed with aq. sodium bicarbonate (100 ml) and water (2 x 100 ml) and then dried (phase separator) and the solvent removed in vacuo to give the title compound (4.126 g) as a colourless oil. 6H (400 MHz, methanol-d 4 ) 1.40 (3H, t), 4.41 (2H, quart), 7.76 (1H, 30 d), 8.22 (1H, dd), 8.34 (1H, d). 85 WO 2008/074821 PCT/EP2007/064185 Description for D99 Methyl 3-chloro-4-(propyloxy)benzoate (D99) 0 Cl 0 Methyl 4-hydroxy-3-chlorobenzoate (10 g, 53.6 mmol) was dissolved in DMF (110 5 ml) and then potassium carbonate (14.8 g, 107.2 mmol) was added followed by n propyliodide (10.4 ml, 107.2 mmol). The reaction was heated to 70 'C overnight, filtered and then the fitrate was partitioned between EtOAc and water. The organic layer was separated, dried and evaporated to give the title compound as a yellow oil (12.37 g). 6H (400 MHz, d 6 -DMSO) 1.00 (3H, t), 1.72-1.92 (2H, m), 3.82 (3H, s), 4.10 10 (2H, t), 7.24 (1H, d), 7.85-8.10 (2H, m). MS (ES) C 1 1

H

1 3 35

CIO

3 requires 228; found 229 (MH*). Description for D100 3-Chloro-4-(propyloxy)benzoic acid (D100) 0 OH Cl 15 0 A solution of methyl 3-chloro-4-(propyloxy)benzoate (D99) (12.22 g, 0.053 mol) in ethanol (40 ml) and 2M NaOH aq. (40 ml) was heated at 60 'C for 3 hours. The reaction was allowed to cool and then left at room temperature over the weekend. The reaction mixture was poured into a mixture of dilute aq. HCI and EtOAc. The 20 organic layer was separated, dried and evaporated to give a solid which was triturated with ether to give the title compound as a white solid (7.7 g). 6H (400 MHz, d 6 -DMSO) 1.00 (3H, t), 1.67-1.87 (2H, m) 4.10 (2H, t), 7.24 (1H, d), 7.84-8.06 (2H, m), 12.97 (1H, br s). MS (ES) C 10

H

11 3 5

CIO

3 requires 214; found 213 (M-H*). 86 WO 2008/074821 PCT/EP2007/064185 Description for D101 Ethyl 3-(3-chloro-5-{5-[3-chloro-4-(propyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H indol-1 -yl)propanoate (D1 01) Cl O-N Cl O N N

CO

2 Et 5 3-Chloro-4-(propyloxy)benzoic acid (D100) (150mg, 0.70 mmol) stirring in DMF was treated with EDC (146mg, 0.76 mmol) followed by HOBt (104mg, 0.76 mmol). The resultant solution was stirred and ethyl 3-{3-chloro-5-[(hydroxyamino)(imino)methyl] 1H-indol-1-yl}propanoate (D96) (216mg, 0.70 mmol) added. Heated mixture at 80 C until reaction was complete. Work up obtained the title compound as 160 mg of pale 10 cream solid. 6H (400 MHz, d 6 -DMSO) 1.03 (3H, t), 1.10 (3H, t), 1.77-1.86 (2H, m), 2.90 (2H, t), 4.05 (2H, q), 4.18 (2H, t), 4.49 (2H, t), 7.40 (1H, d), 7.74 (1H, s), 7.81 (1H, d), 7.91 (1H, dd), 8.15 (1H, dd), 8.22-8.23 (2H, m). MS (ES) C 24

H

23 35 Cl 2

N

3 0 4 requires 487; found 488 (MH*). 15 The following compounds were prepared by similar methods to those described above. The reactions were worked up by partitioning the crude material between ethyl acetate and aq. sodium bicarbonate, separating the organic layer, drying it and evaporating to dryness. The compounds were purified by trituration or normal phase chromatography. 20 Structure precursor Name MH* 87 WO 2008/074821 PCT/EP2007/064185 D102 H 3 C-O D96 ethyl 3-(3-chloro-5-{5- 460 [3-chloro-4 ci (methyloxy)phenyl] cl 1,2,4-oxadiazol-3-yl} SN 1H-indol-1 ,N yl)propanoate NN D103 H 3 C-O D96 ethyl 3-(3-chloro-5-{5- 494 F [4-(methyloxy)-3 (trifluoromethyl)pheny F F N CI I]-1,2,4-oxad iazol-3 0, yl}-lH-indol-1 N N yl)propanoate 0 D104 HC D96 ethyl 3-[3-chloro-5-(5- 479 CH {3-cyano-4.[(1 methylethyl)oxy]phen yl}-1,2,4-oxadiazol-3 N CI yl)-1 H-indol-1 N yl]propanoate 0,N N N8 0 88 WO 2008/074821 PCT/EP2007/064185 D105 o D96 ethyl 3-(3-chloro-5-{5- o=N [4-nitro-3 F (trifluoromethyl)pheny I]-1,2,4-oxad iazol-3 F F CI yl}-1H-indol-1 /0\ yl)propanoate N N, 0 0 Description for D106 Ethyl 3-(5-{5-[3-bromo-4-(methyloxy)phenyl]-1,2,4-oxadiazol-3-yI}-3-chloro-1H indol-1 -yl)propanoate (D1 06) Br N N 5

CO

2 Et The 3-bromo-4-(methyloxy)benzoic acid (commercial: ICN) (243mg, 1.05 mmol) stirring in DMF (10ml) was treated with EDC (219mg, 0.1.14 mmol) followed by HOBt (156mg, 0.1.14 mmol). The resultant solution was stirred for 10 minutes. Added ethyl 3-{3-chloro-5-[(hydroxyamino)(imino)methyl]-1 H-indol-1-yl}propanoate (D96) 10 (324mg, 1.05 mmol) and stirred at RT for 45 minutes. The solution was heated at 80 0C for 4 hours then left standing overnight. The solution was heated at 80 0C for a further 4 hours to give one major product. Evaporated off the DMF, added EtOAc (50ml) and washed with water (50ml). The EtOAc was washed with sat. aqueous sodium hydrogen carbonate (50ml) and water (50ml) then dried over MgSO 4 . 15 Evaporated off the solvent and crystallised from ethanol to yield the title compound as 280mg of cream solid. 6H (400 MHz, d 6 -DMSO) 1.10 (3H, t), 2.90 (2H, t), 3.99 4.05 (5H, m), 4.49 (2H, t), 7.38 (1H, d), 7.74 (1H, s), 7.80 (1H, d), 7.97 (1H, d), 8.21 8.23 (2H, m), 8.36 (1H,d). MS (ES) C 22

H

19 81 Br 35

CIN

3 0 4 requires 505; found 506 (MH*). 89 WO 2008/074821 PCT/EP2007/064185 Description for D107 Ethyl 3-(3-chloro-5-{5-[6-(methyloxy)-3-biphenylyl]-1,2,4-oxadiazol-3-yI}-1 H indol-1 -yl)propanoate (D1 07) O \N N 5

CO

2 Et Ethyl 3-(5-{5-[3-bromo-4-(methyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-3-chloro-1H-indol 1-yl)propanoate (D106) (212mg, 0.42 mmol), phenyl boronic acid (104mg, 0.84 mmol), Pd(PPh 3

)

4 (20mg) and 2N aq. sodium carbonate solution (3ml, 6mmol) were suspended in DME (6ml) and heated at 90 0C for 2 hours. Added phenyl boronic acid 10 (30mg, 0.24 mmol) and Pd(PPh 3

)

4 (20mg) and heated at 90 0C for a further 2 hours. Added EtOAc (70ml) and washed with water (100ml). Dried over MgSO 4 and evaporated off the solvent. The residue was crystallised from ethanol to yield the title compound as 90mg of light tan solid. MS (ES) C 28

H

24 3 5

CIN

3 0 4 requires 501; found 502 (MH*). 15 Description for D108 Ethyl 3-{3-chloro-5-[5-(3-chloro-4-hydroxyphenyl)-1,2,4-oxadiazol-3-yi]-1 H indol-1 -yl}propanoate (D108) Cl HO N 0 90 WO 2008/074821 PCT/EP2007/064185 3-Chloro-4-hydroxybenzoic acid (commercial) (240mg, 1.40 mmol) in dry DMF (8ml) was treated with EDC (292mg, 1.52 mmol) and HOBt (208mg, 1.52 mmol) and stirred for 5 minutes. Added ethyl 3-{3-chloro-5-[(hydroxyamino)(imino)methyl]-1H indol-1-yl}propanoate (D96) (432mg, 1.40 mmol) and stirred at RT for 30 minutes. 5 The reaction mixture was heated at 80 0C for 7 hours. Added EtOAc (70ml) and washed with water (70ml), sat. aq, sodium hydrogen carbonate (70ml) and water (70ml). Dried over MgSO 4 and evaporated off the solvent. The residue was subjected to chromatography using a biotage (EtOAc/hexane 1:2) to obtain the title compound as 200mg of white solid. 6H (400 MHz, d 6 -DMSO) 1.10 (3H, t), 2.91 (2H, t), 4.04 (2H, 10 q), 4.50 (2H, t), 7.67-7.70 (2H, m), 7.75 (1H, s), 7.80-7.81 (2H, m), 7.94 (1H, dd), 8.22-8.25 (1H, m), 10.95 (1H, broad s). MS (ES) C 2 1

H

17 35 C1 2

N

3 0 4 requires 445; found 446 (MH*). Description for D109 15 Ethyl 3-(3-chloro-5-{5-[3-chloro-4-(ethyloxy)phenyl]-1,2,4-oxadiazol-3-yI}-1 H indol-1 -yl)propanoate (D1 09) CI P-N Cl N 0 0 20 To ethyl 3-{3-chloro-5-[5-(3-chloro-4-hydroxyphenyl)-1,2,4-oxadiazol-3-yl]-1H-indol-1 yl}propanoate (D108) (180mg, 0.40 mmol) and K 2

CO

3 (138mg, 1.0 mmol) in dry DMF (3ml) was added ethyl iodide (78mg, 0.50 mmol) and the mixture heated at 80 0C with stirring for 30 minutes. Cooled mixture and added EtOAc (50ml). Washed with water (3x40ml) and dried over MgSO 4 . Evaporated off the solvent and crystallised 25 from ethanol to yield the title compound as 110mg of white solid. 6H (400 MHz, d 6 DMSO) 1.10 (3H, t), 1.42 (3H, t), 2.90 (2H, t), 4.02 (2H, q), 4.27 (2H, q), 4.49 (2H, t), 7.40 (1H, d), 7.74 (1H, s), 7.80 (1H, d), 7.95 (1H, dd), 8.16 (1H, dd), 8.21-8.22 (2H, m). MS (ES) C 2 3

H

2 1 35 Cl 2

N

3 0 4 requires 473; found 474 (MH*). 91 WO 2008/074821 PCT/EP2007/064185 Description for D110 Ethyl 3-[3-chloro-5-(5-{3-chloro-4-[(1 -methylethyl)oxy] phenyl}-1,2,4-oxadiazol-3 yl)-1H-indol-1-yl]propanoate (D1 10) Cl O N N 0 5 0 5 To ethyl 3-{3-chloro-5-[5-(3-chloro-4-hydroxyphenyl)-1,2,4-oxadiazol-3-yl]-1H-indol-1 yl}propanoate (D108) (180mg, 0.40 mmol) and K 2

CO

3 ( 138mg, 1.0 mmol) in dry DMF (5ml) was added isopropyl iodide (85mg, 0.50 mmol) and the mixture stirred at 80 0C for 30 minutes. Cooled mixture and added EtOAc (50ml). Washed with water 10 (2X50ml) and dried over MgSO 4 . Evaporated off the solvent and crystallised from ethanol to yield the title compound as 120 mg of white solid. 6H (400 MHz, d 6 -DMSO) 1.12 (3H, t), 1.37 (6H, d), 2.91 (2H, t), 4.02 (2H, q), 4.50 (2H, t), 4.89-4.98 (1H, m), 7.72-7.85 (5H, m), 7.95-8.00 (1H, m), 8.24 (1H, d). MS (ES) C 24

H

23 35 C1 2

N

3 0 4 requires 487; found 488 (MH*). 15 Description for D111 3-lodo-4-(trifluoromethyl)benzoic acid (D111) 0 OH

F

3 C 3-Amino-4-(trifluoromethyl)benzoic acid (commercially available) (6.5 g, 31.7 mmol) 20 and triiodomethane (37.4 g, 95.1 mmol) were dissolved in THF (300 ml). The reaction mixture was heated to 80 'C and then butyl nitrite (5.56 ml, 47.6 mmol) was added slowly at this temperature. Heating was continued at this temperature for 4 hours and then the reaction was concentrated in vacuo to give the crude product. Purification by column chromatography (hexane to 30% EtOAc in hexane). This 92 WO 2008/074821 PCT/EP2007/064185 material was combined with another batch from a similar reaction performed on 2 g of 3-amino-4-(trifluoromethyl)benzoic acid. The combined material was purified by preparative HPLC to give the title compound (6.1 g). MS C 8

H

4

F

3 10 2 requires 316; found 315 (M-H*). 5 Description for D112 Ethyl 3-(5-{5-[3-iodo-4-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yI}-1H-indol-1 yl)propanoate (D1 12) F N F I N 0 10 D111 (1.0 g, 3.16 mmol) was dissolved in DMF (25 ml) under nitrogen. EDC (0.7 g, 3.7 mmol) and HOBt (0.5 g) were added. The reaction was stirred at room temperature for 15 minutes and then triethylamine (0.87 ml, 6.32 mmol) was added and the reaction was stirred for a further 5 minutes. D52 (0.87 g, 3.16 mmol) was added and the reaction was stirred at room temperature overnight. The reaction was 15 concentrated in vacuo and the resultant oil diluted with ethyl acetate (100 ml). The organic layer was washed with water (2 x 30 ml), dried (Na 2

SO

4 ) and concentrated in vacuo to give the crude product which was purified by column chromatography. The product was eluted in 7% EtOAc in hexane and evaporation afforded the title compound (0.45 g). MS C 2 2

H

1 7

F

3

|N

3 0 3 requires 555; found 556 (MH*). 20 25 93 WO 2008/074821 PCT/EP2007/064185 Description for D113 Ethyl 3-(5-{5-[6-(trifluoromethyl)-3-biphenylyl]-1,2,4-oxadiazol-3-y}-1H-indol-1 yl)propanoate (D1 13) FF /ON IN F N 0 0 5 This material was prepared by a similar method to that used for D107 from D112. MS (ES) C 28

H

22

F

3

N

3 0 2 requires 505; found 506 (MH*). Examples 10 Example 1 3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoic acid (El) 0-N S. -- N\ 0 H N '/ N OH F) F F D3 (38 mg) was dissolved in 2M aqueous NaOH (0.5 ml) and MeOH (0.5 ml) then 15 stirred at RT overnight. LCMS analysis showed 41% product so the reaction mixture was heated to 50 'C and stirred over the weekend. LCMS showed the reaction to be complete. The reaction mixture was evaporated then partitioned between H 2 0 and DCM. The organic layer was extracted with H 2 0. The combined aqueous extracts were acidified to pH = 1 and extracted with DCM. These DCM extracts were dried 20 over MgSO 4 , filtered and evaporated to give the crude product MF105672-149A1 (30 mg). The crude product was purified on a silica cartridge (12+S), eluting with a 0 to 10 % mixture of MeOH in DCM to give the purified product . This was dissolved in CHC13 and evaporated to give the title compound (3 mg) as a white solid. 6H (CDC13, 94 WO 2008/074821 PCT/EP2007/064185 400MHz): 2.92 (2H, t), 4.50 (2H, t), 6.51 (1H, d), 7.24 (1H, d), 7.40-7.53 (6H, m), 7.90 (1 H, s), 8.00 (1 H, d), 8.45 (1 H, s). MS (ES*): C 2 4

H

1 6

F

3

N

3 0 3 S requires 483; found 484 (MH*). 5 Example 1 (alternative procedure) 3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoic acid (El) 0-N F N N OH F S F F D3 (600 mg) was treated with 2 M aq. NaOH (25 ml) and MeOH (25 ml). This mixture 10 was stirred overnight then heated to 50 'C for 6 hours. The MeOH was then evaporated and the remaining solution acidified and extracted with EtOAc (x 3). The combined organic solutions were washed with brine and evaporated to give the crude residue C(302 mg) as an off-white solid. This was triturated with cold MeOH to give the title compound (162 mg) as a grey solid. 6H (d 6 -DMSO, 400MHz): 2.80 (2H, 15 t), 4.46 (2H, t), 6.64 (1H, d), 7.49-7.59 (6H, m), 7.72 (1H, d), 7.85 (1H, dd), 8.22-8.25 (1H, m), 8.31-8.34 (1H, m). MS (ES): C 24

H

16

F

3

N

3 0 3 S requires 483; found 484 (MH*). Example 2 Sodium 3-(5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-lH 20 indol-1-yl)propionate (E2) 0-N N Na NN F 0 F F El (30 mg) was dissolved in EtOAc (1 ml), treated with 2M aqueous NaOH (40 ul), diluted with H 2 0 (1 ml) and extracted with EtOAc (3 x 5 ml), using a small volume of brine during the third extraction to aid phase separation. The combined organics 25 were evaporated to give the title compound (37 mg) as a green solid. 6H (methanol d 4 , 400MHz): 2.68 (2H, t), 4.48 (2H, t), 6.55 (1H, d), 7.49 (1H, d), 7.45-7.56 (5H, m), 7.62 (1H, d), 7.92 (1H, d), 8.03 (1H, s), 8.35 (1H, s). MS (ES*): C 2 4

H

16

F

3

N

3 0 3 S requires 483; found 484 (MH*). 95 WO 2008/074821 PCT/EP2007/064185 Example 3 3-[5-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-y)-1H-indol-1 yl]propanoic acid (E3) ci O-N N \_ 0H O N OH 5 D6 MF105672-178A2 (38 mg) was dissolved in EtOH, treated with 12.5 M aqueous NaOH (2 ml) and stirred at RT for 4 hours. The reaction mixture was evaporated, re dissolved in H 2 0 and washed with diethyl ether. The aqueous solution was acidified then extracted with DCM. The DCM solutions were combined, dried over MgSO 4 , filtered and evaporated to give the title compound MF105672-181A1 (5 mg) as a pale 10 yellow solid. 6H (CDC13, 400MHz): 1.44 (6H, d), 2.94 (2H, t), 4.51 (2H, t), 4.73 (1H, septet), 6.61 (1H, d), 7.07 (1H, d), 7.22 (1H, d), 7.45 (1H, d), 7.94 (1H, d), 8.07 (1H, d), 8.27 (1H, s), 8.47 (1H, s). MS (ES): C 22

H

20

CIN

3 0 4 requires 425; found 426 (MH*). Example 4 15 Sodium 3-[3-Chloro-5-(5-{3-chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4 oxadiazol-3-yI)-1H-indol-1-yl]propanoate (E4) C C 0 / N~0 2 Na D7 (200 mg) and Cs2CO3 (336 mg) were placed in a microwave vial, treated with 20 DMF (2.8 ml) and ethyl 3-bromopropionate (99 ul) and sonicated for 10 minutes. The mixture was then heated to 120 'C in a microwave reactor for 25 mins. The reaction mixture was then evaporated, re-dissolved in MeOH (10 ml) and treated with 2 M aq. NaOH (10 ml). This mixture was sonicated briefly and then heated to 50 'C overnight. The reaction mixture was then evaporated, diluted with H 2 0 (70 ml) and 25 extracted with EtOAc, adding NaCl and acetone to improve the extraction. The organic extracts were evaporated to give the crude product which was acidified with HCI to give the free-acid. This was insufficiently soluble for purification by chromatography and so was triturated with MeOH, treated with 2M aq. NaOH (1.5 eq.), evaporated, dissolved in EtOAc, filtered and evaporated to give the title 30 compound (56 mg) as a brown solid. 6H (methanol-d 4 , 400MHz): 1.42 (6H, d), 2.66 (2H, t), 4.47 (2H, t), 4.82 (1H, m), 7.29 (1H, d), 7.44 (1H, s), 7.65 (1H, d), 7.98 (1H, 96 WO 2008/074821 PCT/EP2007/064185 d), 8.12 (1H, d), 8.20 (1H, s), 8.30 (1H, s). MS (ES): C 2 2

H

19 35 C1 2

N

3 0 4 requires 459; found 460 (MH*). Example 5 5 3-(3-Chloro-5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yI} 1H-indol-1-yl)propanoic acid (E5) ci 0-N N s '/ N 0 2 H F S F F D8 (86 mg), 3-bromopropionate (52 mg), Cs 2

CO

3 (126 mg) and DMF (1 ml) were placed in a microwave vial and stirred at 131 'C in the microwave reactor for 1.5 10 hours. The reaction mixture was then evaporated to dryness and treated with 2M aq. NaOH and EtOH (20 ml). This solution was stirred at 50 'C for 4 hours and then neutralised with HCI and evaporated to remove the EtOH. The aqueous solution was then extracted twice with EtOAc and the combined extracts evaporated. The residue was dissolved in DMSO, filtered, treated with MeCN causing precipitation of the 15 product which was filtered and washed with MeCN to give the title compound (23 mg) as an off-white solid. 6H (d 6 -DMSO, 400MHz): 2.47-2.57 (solvent + 2H) 4.37 (2H, t), 7.51-7.59 (5H, m), 7.72 (1H, s), 7.76 (1H, d), 7.89 (1H, d), 8.17 (1H, s), 8.25 (1H, s). MS (ES): C 24

H

1 5

CIF

3

N

3 0 2 S requires 517; found 516 (M-H*). 20 Example 6 3-(4-{5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-lH-indol-1 yl)propanoic acid (E6) 0-N N -\C \ N F S F F D10 (85 mg, 0.207 mmol) was placed in a microwave vial with Cs2CO3 (135 mg) and 25 DMF (1 ml). This was stirred briefly and ethyl bromopropionate (40 ul) was added. The mixture was heated at 130 'C for 1.5 hours in the microwave reactor. The reaction mixture was transferred to a flask containing 2 M aqueous NaOH (5 ml) and EtOH (5 ml), then stirred at room temperature overnight. The mixture was then evaporated and the residue acidified to pH = 2.5 with 2 M aqueous HCl. This solution 97 WO 2008/074821 PCT/EP2007/064185 was extracted with EtOAc twice and the combined extracts evaporated to give a yellow residue which was purified by MDAP to give the title compound (50 mg) as a white solid. 6H (CDC13, 400MHz): 2.93 (2H, t), 4.50 (2H, t), 7.26 (1H, s), 7.33 (1H, d), 7.37 (1 H, ap t), 7.45-7.52 (5H, m), 7.55 (1 H, d), 7.93 (1 H, s), 8.04 (1 H, d). MS (ES): 5 C 2 4

H

1 6

F

3

N

3 0 3 S requires 483; found 482 (M-H*). Example 7 3-[4-(5-{3-Chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1 H-indol 1-yl]propanoic acid (E7) 0-N N O F CI F N OH 10 F 3-Chloro-4-[(trifluoromethyl)oxy]benzoic acid (commercial source) (131 mg), EDCI (114 mg) and HOBT (81 mg) were dissolved in DMF (2.5 ml) and stirred at RT for 10 minutes. Ethyl 3-{5-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D57) (150 mg) in DMF (2.5 ml) was added and stirring continued at RT for 2 hours. The 15 mixture was then heated at 80 'C overnight. The reaction mixture was evaporated to dryness then extracted with EtOAc (2 x 25 ml) from H 2 0 (25 ml). The combined organic solutions were evaporated to dryness and the residue treated with EtOH and 2 M aq. NaOH (1:1 mixture, 20 ml). This mixture was stirred at 50 'C for 2 hours then evaporated to remove the EtOH. The resultant precipitate was filtered off and 20 washed with a mixture of H 2 0 and EtOH then 2 M HCI. The residue was recrystallised from hot EtOH to give the title compound (62 mg) as a white solid. 6H (d 6 -DMSO, 400MHz): 2.81 (2H, t), 4.50 (2H, t), 7.08 (1H, d), 7.36 (1H, apparent t), 7.61 (1H, d), 7.83 (1H, d), 7.89 (1H, d), 7.96 (1H, d), 8.32 (1H, dd), 8.50 (1H, d). MS (ES-): C 20

H

13 35

CIF

3

N

3 0 4 requires 451; found 450 (M-H*). 25 Example 8 3-[4-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-y)-1H-indol-1 yl]propanoic acid (E8) 0-N N O 8 OH 0 98 WO 2008/074821 PCT/EP2007/064185 3-chloro-4-[(1-methylethyl)oxy]benzoic acid (D4) (117 mg) was added to EDCI (114 mg) and HOBT (81 mg) dissolved in DMF (2.5 ml). This was stirred at RT for 10 minutes and then ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D57) (150 mg) in DMF (2.5 ml) was added and stirring continued at RT for 2 hours 5 then at 80 'C overnight. The reaction mixture was evaporated to dryness and extracted from H 2 0 (25 ml) with EtOAc (2 x 25 ml). The combined organics were evaporated and treated with 2 M aq. NaOH (10 ml) and EtOH (10 ml), stirred at 50 .C for 2 hours then evaporated to remove the EtOH. The remaining solution was acidified, filtered and the precipitate washed with EtO/H 2 0 then recrystallised from 10 hot EtOH/H 2 0 then from DMSO. Washing with Et 2 0 and MeOH gave the title compound (46 mg) as a white solid. 6H (d 6 -DMSO, 400MHz): 1.37 (6H, d), 2.81 (2H, t), 4.50 (2H, t), 4.89 (1H, septet), 7.08 (1H, d), 7.35 (1H, apparent t), 7.46 (1H, d), 7.60 (1H, d), 7.81 (1H, d), 7.94 (1H, d), 8.15 (1H, dd), 8.23 (1H, d). MS (ES-):

C

22

H

20 35

CIN

3 0 4 requires 425; found 424 (M-H*). 15 Example 9 3-[4-(5-{5-Chloro-6-[(1 -methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yI)-1 H indol-1-yl]propanoic acid (E9) 0-N N O N OH 0 N 20 Ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1 H-indol-1 -yl}propanoate (D57) (150 mg) in DMF (2.5 ml) was added to a solution of 5-chloro-6-[(1-methylethyl)oxy]-3 pyridinecarboxylic acid (D61) (118 mg), HOBT (81 mg) and EDCI (114 mg) which had been stirring at RT for 10 minutes in DMF (2.5 ml). The resultant mixture was stirred at RT for 2 hours then heated at 80 'C for three days. The reaction mixture 25 was evaporated to dryness and extracted from H 2 0 (25 ml) with EtOAc (2 x 25 ml). The combined organics were evaporated and the residue stirred in EtOH/2 M aq. NaOH (1:1 mixture, 20 ml) at 50 'C for 2 hours. The EtOH was evaporated and the precipitate removed by filtration. This was acidified then purified by MDAP to give the title compound (48 mg) as an off white solid. 6H (d 6 -DMSO, 400MHz): 1.40 (6H, d), 30 2.80 (2H, t), 4.50 (2H, t), 5.46 (1H, septet), 7.08 (1H, d), 7.36 (1H, apparent t), 7.60 (1H, d), 7.82 (1H, d), 7.95 (1H, d), 8.60 (1H, d), 8.97 (1H, d). MS (ES-):

C

21

H

19 3 5

CIN

4 0 4 requires 426; found 425 (M-H*). 99 WO 2008/074821 PCT/EP2007/064185 Example 9 (alternative procedure) 3-[4-(5-{5-Chloro-6-[(1 -methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yI)-1 H indol-1-yl]propanoic acid (E9) 0 Cl N\ / /0 N 7 N N OH 0 5 Ethyl 3-[4-(5-{5-chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1 H indol-1-yl]propanoate (D62) (1.1 g, 2.418 mmol) was dissolved in a mixture of 1,4 dioxane (100 ml) and ethanol (100 ml). Water (50.0 ml) was added followed by 2N sodium hydroxide (2.418 ml, 4.84 mmol). The mixture was stirred at RT for one and a half hours to give a single product. Evaporated off most of the solvent, acidified with 10 glacial acetic acid, added water (50ml) and extracted product into EtOAc (200ml). Washed with water (30ml) and dried over MgSO 4 . The solvent was evaporated off until a white precipitate was formed. The solid was filtered off and washed with ether. Mass of title compound obtained was 780mg. 6H (400 MHz, d 6 -DMSO) 1.38 (6H, d), 2.81 (2H, t), 4.50 (2H, t), 5.41-5.51 (1H, m), 7.07 (1H, dd), 7.36 (1H, t), 7.59 (1H, d), 15 7.81 (1H, d), 7.94 (1H, dd), 8.58 (1H, d), 8.96 (1H, d), 12.40 (1H, broad s). MS (ES)

C

21

H

19 3 5

CIN

4 0 4 requires 426; found 427 (MH*). 20 100 WO 2008/074821 PCT/EP2007/064185 Example 10 Sodium 3-[5-(5-{3-chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-y) 1H-indol-1-yl]propanoate (E10) ci 0-N 0 / N ONa' 5 (D5) (200 mg) was dissolved in DMF (4 ml), treated with Cs2CO3 (368 mg) and then ethylbromopropionate (109 pl). The resultant mixture was heated to 120 'C in a microwave reactor for 2 hours. The reaction mixture was decanted from the insoluble residue and evaporated to dryness to give a pale orange oil 10 This oil was dissolved in EtOH (2 ml) and treated with 2 M aqueous NaOH (2 ml). This produced a white precipitate so a further portion of EtOH (2 ml) was added to produce a homogeneous solution. The resultant mixture was heated to 60 'C for 1 hour then stood at RT overnight. The reaction mixture was evaporated to dryness, re-dissolved in H 2 0 (10 ml), treated with brine (2 ml) and extracted with a mixture of 15 EtOAc and MeCN (2 x 20 ml). Evaporation gave the crude product (313 mg) as a pale green solid. This was dissolved in MeOH (5 ml), filtered and evaporated then triturated with Et 2 0 to give the title compound (247 mg) as a pale green solid. 6H (methanol-d 4 , 400MHz): 1.42 (6H, d), 2.68 (2H, t), 4.48 (2H, t), 4.83 (1H, septet), 6.55 (1H, dd), 7.30 (1H, d), 7.38 (1H, d), 7.61 (1H, d), 7.91 (1H, dd), 8.12 (1H, dd), 20 8.21 (1 H, d), 8.34 (1 H, dd). MS (ES-): C 22

H

20

CIN

3 0 4 requires 425 found 424 (M-H*). The following compounds were prepared in an similar manner to example 1. The solvent for the hydrolysis step was either methanol or ethanol and the reaction temperature between room temperature and 60 'C. In some cases the reactions 25 were worked up by extracting the product or acidified product into an organic solvent and in other cases the final compound precipitated from the aqueous layer and was isolated by filtration. Purification was by MDAP, trituration or recrystallisation. 30 101 WO 2008/074821 PCT/EP2007/064185 Example Structure Name Comments MS O-N (5-{5-[4-phenyl-5 NiF(trifluoromethyl)-2 E11 F N thienyl]-1,2,4-oxadiazol- oy4 470 (MH*) F N OH 3-yl}-1H-indol-1- of 042 yl)acetic acid 0 HC CH3 0 C / sodium 3-[3-bromo-5 N (5-{3-chloro-4-[(1- 504 (M-H E12 N N methylethyl)oxy]phenyl} Hydrolysis 35C, & -1,2,4-oxadiazol-3-yl)- of D43 8B Na 1H-indol-1- Br) yl]propanoate H3C )CH3 0 C \ / sodium 5-[5-(5-{3 ... N chloro-4-[(1 1 N3 methylethyl)oxy]phenyl} Hydrolysis 454 (MH+ E13 N, -1,2,4-oxadiazol-3-yl)- of D44 for 35CI) 1H-indol-1 yl]pentan'oate 0 4-[5-(5-{3-chloro-4-[(1 HO methylethyl)oxy]phenyl} yrlsi 4 M + E1 HHydrolysis 440 (MC) E14 o -1,2,4-oxadiazol-3-yl)- of 045 for 35Cl) 1H-indol-1-yl]butanoic acid (2R)-3-[5-(5-{3-chloro H3C-jo N2R El15 methylethyl)oxy]phenyl} Hydrolysis 440 (MH+ -1,2,4-oxadiazol-3-yl)- of D46 for 35C, 1H-indol-1-yl]-2 methylpropanoic acid 102 WO 2008/074821 PCT/EP2007/064185 CH (2S)-3-[5-(5-{3-chloro H3C 0 E16 OH methylethyl)oxy]phenyl} Hydrolysis 440 (MH* 0 -1,2,4-oxadiazol-3-yl)- of D47 for 35CI) 1H-indol-1-yl]-2 methylpropanoic acid F ' F F \ NN 2,2-dimethyl-3-(5-{5-[4 F

-

phenyl-5 E1 7CH (trifluoromethyl)-2- Hydrolysis 512 (MH+) HCO O thienyl]-1,2,4-oxadiazol- of D48. 3-yl}-1H-indol-1 yl)propanoic acid Example 18 3-[5-(5-{3-Chloro-4-[(1 -methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-y)-1 H-indol-1 yl]-2,2,3-trifluoropropanoic acid (E18) 0-N O F OH 5 F F D5 (200 mg), Cs 2

CO

3 (552 mg) and DMF (2.8 ml) were stirred at RT and treated with 3-bromo-2,2,3-trifluoropropanoic acid (175 mg). This mixture was heated at 140 'C for 1 hour in a microwave reactor. 2 further equivalents of Cs2CO3 (368 mg) were added and heating continued at 140 'C for 10 hours. The reaction mixture was then 10 evaporated, treated with H 2 0, shaken and filtered to give a brown solid residue. This was purified by MDAP to give the title compound (12 mg) as a white solid. 6H (methanol-d 4 , 400MHz): 1.42 (6H, d), 4.83 (1H, septet), 6.87 (1H, d), 7.29 (1H, d), 7.45 (1H, d), 7.54 (1H, d), 7.61 (1H, d), 7.80 (1H, d), 8.06 (1H, d), 8.11 (1H, d), 8.19 8.22 (1H, m), 8.44 (1H, s). 15 20 103 WO 2008/074821 PCT/EP2007/064185 Example 19 Sodium 4-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yI)-lH indol-1 -yl]butanoate (El 9) 5 0

N

/ 0 N N N 0 0 Na To a solution of ethyl 4-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol 10 3-yl)-1H-indol-1-yl]butanoate (D65) (1.42g, 3.09 mmol) in a mixture of dioxan (70ml) and ethanol (70ml) was treated with 2N sodium hydroxide (1.86ml, 3.71 mmol) followed by water (35ml). The solution was stirred at RT for 4 hours. Evaporated off most of the solvent and filtered off the white solid from the remaining solvent. Washed the solid with water followed by ether and dried to give 580mg of the title 15 compound. 6H (400 MHz, methanol-d 4 ) 1.45 (6H, d), 2.09-2.22 (4H, m), 4.30 (2H, t), 4.92-4.98 (1H, m), 7.15 (1H, d), 7.31 (1H, t), 7.38-7.43 (2H, m), 7.69 (1H, d), 7.95 (1H, d), 8.43-8.46 (2H, m). MS (ES) C 24

H

2 2

N

4 0 4 requires 430; found 431 (MH*). 20 104 WO 2008/074821 PCT/EP2007/064185 Example 20 Sodium 3-[5-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yI)-lH indol-1 -yl]propanoate N - N N 0 5 0 Na Ethyl 3-[5-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 yl]propanoate (D53) (150mg, 0.38 mmol) was dissolved in ethanol (25ml) by warming to 60 0C. Allowed solution to cool to RT then added 2N sodium hydroxide (3ml, 6 mmol). The solution was stirred at RT for 30 minutes. LC/MS showed a single 10 product. Evaporated off the ethanol and filtered off the solid which precipitated out of solution. Mass of title compound as a light tan solid obtained on drying was 50mg. 6H (400 MHz, d 6 -DMSO) 1.45 (6H, d), 2.67 (2H, t), 4.48 (2H, t), 4.92-4.98 (1H, m), 6.54 6.55 (1H, m), 7.34 (1H, d), 7.38 (1H, d), 7.60 (1H, d), 7.91 (1H, dd), 8.35 (1H, d), 8.41-8.46 (2H, m). MS (ES) C 2 3

H

2 0

N

4 0 4 requires 416; found 417 (MH*). 15 Example 21 Sodium 3-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yI)-1H indol-1 -yl]propanoate (E21) 105 WO 2008/074821 PCT/EP2007/064185 N -0 / 0 N N N 0 0 Na Ethyl 3-[4-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1 yl]propanoate (D63) (81mg, 0.18 mmol) was dissolved in ethanol by warming to 50 C. Added 2N sodium hydroxide (0.25ml, 0.5 mmol) followed by water (2ml), warmed 5 to 50 0C to give a clear solution then left standing at RT for 30 minutes. LC/MS showed a single product. The ethanol was evaporated off to obtain a precipitate which was filtered off and dried. Mass of title compound as a pale brown solid obtained was 60 mg 6H (400 MHz, d 6 -DMSO) 1.39 (6H, d), 2.32 (2H, t), 4.39 (2H, t), 4.96-5.00 (1H, m), 7.01 (1H, d), 7.31 (1H, t), 7.56-7.61 (2H, m), 7.74 (1H, d), 7.91 10 (1H, d), 8.45 (1H, dd), 8.55 (1H, d). MS (ES) C 2 3

H

2 0

N

4 0 4 requires 416; found 417 (MH*). 15 20 106 WO 2008/074821 PCT/EP2007/064185 Example 22 Sodium 3-(4-{5-[2-(trifluoromethyl)-4-biphenyly]-1,2,4-oxadiazol-3-y}-1H-indol 1-yl)propanoate (E22) F /F F / 0 N N N 0 0 + Na 5 Ethyl 3-(4-{5-[2-(trifluoromethyl)-4-biphenylyl]-1,2,4-oxadiazol-3-yl}-1 H-indol-1 yl)propanoate (D64) (15mg, 0.31 mmol) was dissolved in ethanol (50ml) by warming to 40 'C for 10 minutes then 2N sodium hydroxide (4ml, 8 mmol) was added followed by water (8ml). The solution was left standing for 1 hour. Evaporated off the ethanol and filtered off the off-white solid. Mass of title compound as a beige 10 obtained on drying was 42 mg. 6H (400 MHz, methanol-d 4 ) 2.69 (2H, t), 4.53 (2H, t), 7.17-7.18 (1H, m), 7.32-7.40 (3H, m), 7.46-4.49 (4H, m), 7.66 (1H, d), 7.75 (1H, d), 8.02 (1H, d), 8.53 (1H, dd), 8.63 (1H, d). MS (ES) C 26

H

18

F

3

N

3 0 3 requires 477; found 478 (MH*). 15 20 107 WO 2008/074821 PCT/EP2007/064185 Example 23 Sodium 3-(4-{5-[4-cyclohexyl-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl} 1 H-indol-1 -yl)propanoate (E23) 5 CF3 / \ NN N N 0 Na Ethyl 3-(4-{5-[4-cyclohexyl-3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1 yl)propanoate (D69) (63 mg, 0.123 mmol) was dissolved in ethanol (8 ml) and 10 sodium hydroxide (2M, 0.5 ml, 1.000 mmol) was added. The reaction was heated at 40 0C for 18 h. LCMS showed complete conversion to product. The reaction mixture was concentrated in vacuo and the white solid filtered off and washed with water. On filtration, much compound redissolved and passed through, so solid and filtrate were combined and separated between dichloromethane (10 mL) and 2M HCI (3 mL). 15 The aqueous phase was extracted with further dichloromethane (10 mL). The organic phases were isolated by phase separator, combined and the solvent removed in vacuo. The solid was then dissolved in acetonitrile and water with addition of an equimolar amount of sodium hydroxide (2M, 53 pL) before the solution was freeze-dried to give the title compound (42 mg) as a white solid. 6H (methanol 20 d 4 , 400 MHz): 8.48 (1H, d), 8.43 (1H, dd), 7.98 (1H, dd), 7.86 (1H, d), 7.73 (1H, d), 7.46 (1H, d), 7.32 (1H, app. t), 7.15 (1H, dd), 4.52 (2H, t), 3.04 (1H, t), 2.69 (2H, t), 108 WO 2008/074821 PCT/EP2007/064185 2.0-1.8 (5H, m), 1.63 (2H, dd), 1.53-1.37 (3H, m). MS (ES) C 2 6

H

2 4

F

3

N

3 0 3 requires 483; found 482 (M-H*). Example 24 5 Sodium 3-(4-{5-[4-[(1 -methylethyl)oxy]-3-(trifluoromethyl)phenyl]-1,2,4 oxadiazol-3-yI}-lH-indol-1-yl)propanoate (E24) 0 / ~ CF 3 0 N N N 0 Na 0 To a suspension of ethyl 3-(4-{5-[4-[(1-methylethyl)oxy]-3-(trifluoromethyl)phenyl] 10 1,2,4-oxadiazol-3-yl}-1H-indol-1-yl)propanoate (D72) (81 mg, 0.17 mmol) in ethanol (8mL) was added aqueous sodium hydroxide (2M, 0.8 mL, 1.6 mmol) and the reaction heated to 50 'C to dissolve the reagents before heating at 40 'C for 1 h. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (20 mL) and water (20 mL) and acidified with aqueous hydrochloric acid (2M). The 15 aqueous phase was extracted with further ethyl acetate (2 x 20 mL) and the combined organic extracts dried (phase separator) and concentrated in vacuo. The solid was then dissolved in acetonitrile and water with addition of an equimolar amount of sodium hydroxide (2M) before the solution was freeze-dried to give the title compound (57 mg). 6H (d 6 -DMSO, 400 MHz): 8.44 (1H, dd), 8.35 (1H, d), 7.93 20 (1 H, dd), 7.74 (1 H, d), 7.65-7.54 (2H, m), 7.31 (1 H, app. t), 7.00 (1 H, dd) 4.99 (1 H, septet), 4.38 (2H, t), 2.34 (2H, t), 1.36 (6H, d). MS (ES): C 2 3

H

2 0

F

3

N

3 0 4 requires 459; found 460 (MH*). 109 WO 2008/074821 PCT/EP2007/064185 The following examples were prepared by similar hydrolysis reactions to those described above. At least two equivalents of sodium hydroxide were used. The solvent was either ethanol or methanol. In some cases a cosolvent (dichloromethane or dioxane) was used to aid dissolution of the starting material. The reactions were 5 carried out at a temperature between room temperature and 50 'C. In some cases the some or all of the solvent was removed after the reaction was complete. The reactions were either worked up by partitioning between an organic and an aqueous layer or by filtering the solid product from the aqeuous solvent. In some cases the crude products were purified by trituration. Products were either isolated as the acid 10 or the sodium salt. Structure precursor Name MS E25 CH, D73 sodium [4-(5-{3-chloro-4- 412 (MH+ for ci 0 [(1- 35CI) methylethyl)oxy]phenyl} H, 1,2,4-oxadiazol-3-yl)-1H indol-1-yl]acetate 0 /I \ N N N Na 04 E26 N D74 sodium [4-(5-{3-cyano-4- 403 (MH*) CH3 methylethyl)oxy]phenyl} CH, 1,2,4-oxadiazol-3-yl)-1H indol-1-yl]acetate 0 N N N N. 0 NaO 0 110 WO 2008/074821 PCT/EP2007/064185 E27 F D76 sodium 3-(4-{5-[2'-fluoro- 496 (MH*) F F / 2-(trifluoromethyl)-4 biphenylyl]-1,2,4 oxadiazol-3-yl}-1 H-indol 1-yl)propanoate I x N NNa C 0 E28 CH, D77 sodium 4-[4-(5-{3-chloro- 440 (MH+ for ci - 4_ 1- 35CI) CH, methylethyl)oxy]phenyl} 1,2,4-oxadiazol-3-yl)-1 H 0 indol-1-yl]butanoate N N N Na 0 0 E29 F D78 sodium 4-[4-(5-{3-chloro- 466 (MH+ for CI -~. 35 4 F .- CI) F [(trifluoromethyl)oxy]phen yI}-1,2,4-oxadiazol-3-y) 1H-indol-1-yl]butanoate N _ ~~Na ~ ~_ _ _ _ __ 0 01 WO 2008/074821 PCT/EP2007/064185 E30 D79 4-[4-(5-{5-chloro-6-[(1- 441 (MH+ for CH, methylethyl)oxy]-3- CI) C' pyridinyl}-1,2,4-oxad iazol / \ CH3 N 3-yl)-1H-indol-1 yl]butanoic acid N hydrochloride CIH HO 0 E31 F D80 4-(4-{5-[4-phenyl-5- 498 (MH*) F F (trifluoromethyl)-2 thienyl]-1,2,4-oxadiazol-3 s N yl}-1H-indol-1-yl)butanoic acid 0 N HO 0 E32 D81 4-(4-{5-[2- 492 (MH*) F F (trifluoromethyl)-4 F 'biphenylyl]-1,2,4 oxadiazol-3-yl}-1 H-indol 1-yl)butanoic acid 0 N HO 0 112 WO 2008/074821 PCT/EP2007/064185 E33 D82 3-(4-{5-[4-(methyloxy)-3- 432 (MH*) FF F(trifluoromethyl)phenyl] C 1,2,4-oxadiazol-3-yl}-1 H O 'N indol-1-yl)propanoic acid N I\N HO E34 N CH D83 sodium 4-{4-[5-(3-cyano- 445 (MH*) 0 4-{[(1 R)-1 CH3 methylpropyl]oxy}phenyl) 1,2,4-oxadiazol-3-yl]-1 H 0, \ indol-1-yl}butanoate N Na+ 0 0 E35 N D84 4-{4-[5-(3-cyano-4-{[(1S)- 445 (MH*)

\CH

3 1 CH3 methylpropyl]oxy}phenyl) \ 1,2,4-oxadiazol-3-yl]-1H indol-1-yl}butanoic acid 0 / \ N HO 0 E36 D85 sodium 3-(4-{5-[3-ethyl-4- 445 (MH*) N O Na (1 -piperidinyl)phenyl] o0o 1,2,4-oxadiazol-3-yl}-1 H indol-1 -yl)propanoate 113 WO 2008/074821 PCT/EP2007/064185 E37 D86 sodium 3-{4-[5-(4- 444 (MH*) N cyclohexyl-3 'N O ethylphenyl)-1,2,4 oxadiazol-3-yl]-1 H-indol 1-yl}propanoate E38 D87 3-(4-{5-[5-chloro-6-(1- 438 (MH+ for N N pyrrolidinyl)-3-pyridinyl]- 35CI) 0 ~ OH 1,2,4-oxadiazol-3-yl}-1H N N indol-1-yl)propanoic acid N N E39 D88 4-[4-(5-{3-bromo-4-[(1- 484 (MH+ for N methylethyl)oxy]phenyl}- 79Br) o'N _ 1,2,4-oxadiazol-3-yl)-1

H

HC O N HO indol-1-yl]butanoic acid E40 D89 4-(4-{5-[3-chloro-4-(2- 438 (MH+ for O.-N N O methylpropyl)phenyl]- 35CI) HO 1,2,4-oxadiazol-3-yl}-1 H C CH,/ N indol-1-yl)butanoic acid HC CI E41 CH3 D90 sodium 3-(4-{5-[4-(2- 456 (M-H*) F CH3 methylpropyl)-3 / \ F (trifluoromethyl)phenyl] F 1,2,4-oxadiazol-3-yl}-1 H 0 indol-1 -yl)propanoate N N Na 0 114 WO 2008/074821 PCT/EP2007/064185 E42 CH, D91 4-(4-{5-[3-cyano-4-(2- 429 (MH*) methylpropyl)phenyl] CH/ 1,2,4-oxadiazol-3-yl}-1 H -N indol-1-yl)butanoic acid N N O N 0 OH E43 D92 4-{4-[5-(2-cyano-4- 447 (M-H*) biphenylyl)-1,2,4 oxadiazol-3-yl]-1 H-indol 1-yl}butanoic acid 0 I 4 NN N 0 OH Example 44 3-(3-Chloro-4-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yI} 5 1H-indol-1-yl)propanoic acid (E44) CI 0-N N 0 F S N OH F F This material was prepared in a similar fashion to E5 (from D93) except that the alkylation step took 4.5 h in the microwave and the hydrolysis step was carried out at room temperature overnight. MS (ES): C 24

H

15

CIF

3

N

3 0 3 S requires 517; found 516 (M 10 H*). 115 WO 2008/074821 PCT/EP2007/064185 Example 45 Sodium 3-[3-chloro-5-(5-{3-chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4 oxadiazol-3-yl)-1 H-indol-1 -yl]propanoate(E45) F IF Cl -Nci F CII O-N N 0 0 Na+ 5 To ethyl 3-[3-chloro-5-(5-{3-chloro-4-[(trifluoromethyl)oxy]phenyl}-1,2,4-oxadiazol-3 yl)-1H-indol-1-yl]propanoate (D97) (150mg, 2.9 mmol) in ethanol (1Oml) was added 2N NaOH (2ml, 4 mmol) and the mixture heated at 50 'C for 30 minutes. Evaporated off the ethanol and filtered off the pale cream solid which had precipitated out of the 10 remaining solution. Mass of title compound obtained on drying was 100mg. 6H (400 MHz, d 6 -DMSO) 2.35 (2H, t), 4.35 (2H, t), 7.73-7.75 (2H, m), 7.86 (1H, d), 7.92 (1H, d), 8.22 (1 H, s), 8.30-8.32 (1 H, m), 8.49 (1 H, d). MS (ES) C 20

H

12 35 C1 2

F

3

N

3 0 4 requires 485; found 486 (MH*) 15 Example 46 Sodium 3-(3-chloro-5-{5-[3-chloro-4-(propyloxy)phenyl]-1,2,4-oxadiazol-3-yI} 1 H-indol-1 -yl)propanoate (E46) Cl P-N Cl 0 N N 0 0 + Na 20 116 WO 2008/074821 PCT/EP2007/064185 To ethyl 3-(3-chloro-5-{5-[3-chloro-4-(propyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H indol-1-yl)propanoate (D101) (120mg, 2.5 mmol) in ethanol (10ml) was added 2N NaOH (2ml) and the mixture heated at 50 0C for 30 minutes. Evaporated off the ethanol and filtered off the white solid which had precipitated out of the remaining 5 solution. Mass of title compound obtained on drying was 85mg. 6H (400 MHz, d 6 DMSO) 1.03 (3H, t), 1.77-1.86 (2H, m), 2.34 (2H, t), 4.17 (2H, t), 4.35 (2H,t), 7.40 (1H,d), 7.71-7.74 (2H,m), 7.91 (1H, d), 8.15 (1H,dd), 8.20-8.21 (2H,m). MS (ES)

C

22

H

19 35 C1 2

N

3 0 4 requires 459; found 460 (MH*). 10 The following examples were prepared by a similar method to those described above, using 2-60 equivalents of sodium hydroxide (Table 8). The reactions were worked up by removing the ethanol and filtering the resultant solid or extracting the product into ethyl acetate. If required the products were purified by trituration with ether. 15 Structure precursor Name MS E47 D102 sodium 3-(3-chloro-5-{5- 430, 432 (M [3-chloro-4- H+ for 35C12, HC--O (methyloxy)phenyl]-1,2,4- 35C37Cl) CI \ oxadiazol-3-yl}-1 H-indol -N CI 1-yl)propanoate N Na 117 WO 2008/074821 PCT/EP2007/064185 E48 D103 sodium 3-(3-chloro-5-{5- 466 (MH+ for HC-O [4-(methyloxy)-3- 35CI) F (trifluoromethyl)phenyl] F F N CI 1,2,4-oxadiazol-3-yl}-1H N N indol-1-yl)propanoate o NNa E49 D109 sodium 3-(3-chloro-5-{5- 444, 446 (M [3-chloro-4- H+ for 35C12, H3C (ethyloxy)phenyl]-1,2,4- 3 5 C137C1) 0 oxadiazol-3-yl}-1 H-indol C' \ / 1-yl)propanoate 'N'' 'N Na 0 E50 D104 sodium 3-[3-chloro-5-(5- 451 (MH+ for H3C C{3-CyanO-4-[(1- 35 C) 0 methylethyl)oxy]phenyl} N - / 1,2,4-oxadiazol-3-yl)-1 H -N CI indol-1 -yl]propanoate 0, N 0 Na 0 118 WO 2008/074821 PCT/EP2007/064185 E51 D105 sodium 3-(3-chloro-5-{5- 478, 480 in [4-nitro-3- ES F (trifluoromethyl)phenyl] F F CI 1,2,4-oxadiazol-3-yl}-1H 0, indol-1-yl)propanoate NN Na 0 Example 53 Sodium 3-(3-chloro-5-{5-[6-(methyloxy)-3-biphenyly]-1,2,4-oxadiazol-3-yI}-1H indol-1 -yl)propanoate (E53) 5 O - N N 0 Na 0 Ethyl 3-(3-chloro-5-{5-[6-(methyloxy)-3-biphenylyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1 yl)propanoate (D107) (90mg, 0.18 mmol) was heated in ethanol (10ml) to give a 10 clear solution. This solution was treated with 2N sodium hydroxide (3ml, 6 mmol) and stirred at 50 0C for 30 minutes. Evaporated off the ethanol and filtered off the white solid that precipitated out of solution, washing the solid with a small amount of water and ether. Stirred solid in a small amount of acetone for 1 hour, filtered, washed with a small amount of ether and dried to yield the title compound as 45mg of white solid. 15 6H (400 MHz, d 6 -DMSO) 2.34 (2H, t), 3.91 (3H, s), 4.34 (2H, t), 7.41-7.46 (2H, m), 119 WO 2008/074821 PCT/EP2007/064185 7.48-7.50 (2H, m), 7.57-7.59 (2H, m), 7.63-7.66 (2H, m), 7.80 (1H, d), 8.10 (1H, d), 8.10-8.25 (2H, m). MS (ES) C 2 6

H

20 3

CIN

3 0 4 requires 473; found 474 (MH*). Example 54 5 3-(5-{5-[6-(Trifluoromethyl)-3-biphenyly]-1,2,4-oxadiazol-3-y}-1 H-indol-1 yl)propanoic acid (E54) O--N N N F F OH F0 This material was prepared by a similar method to prepare E53. The solvent was a mixture of ethanol and 1,4-dioxane and 0.071 ml of 2M aq. NaOH was used to 10 hydrolyse 51 mg of D113. MS (ES) C 2 6

H

18

F

3

N

3 0 3 requires 477; found 476 (M-H*). GTPyS binding assay Rat basophilic eukaemia cells (RBL) stably expressing S1 P1 receptor were grown to 15 80% confluency before being harvested into 10ml Phospho-Buffered Saline (PBS) and centrifuged at 1200rpm for 5 minutes. After removal of the supernatant, the pellet was re-suspended and homogenised in 20 volumes assay buffer (20mM HEPES pH 7.4, 100mM NaCl, 10mM MgCl 2 .6H 2 0, 10pM GDP Saponin lOpg/ml). The membrane suspension was further centrifuged for 20 minutes at 20,000rpm re 20 homogenised and spun again. Following the second centrifugation the pellet was re suspended in an appropriate volume (1ml for each flask of cells) and assayed for protein concentration. Concentrated stock of S1 P was sonicated before serial dilutions were prepared from 25 a starting concentration of 10- 5 M. Diluted membranes (10pg/well) were incubated with various concentrations of S1 P and 0.3nM 3 5 S-GTPyS (NEN; specific activity1250 Ci/mmol) in 96 deep well plates. Binding was performed at 300C for 45 minutes and terminated by harvesting the membranes onto GF/B filter plates using a Packard Universal Harvester. After drying the plates for 45 minutes, 50pl of 30 Microscint 0 was added to each well and binding measured on a Topcount NXT (Perkin Elmer). Data was analysed using Graphpad Prism 4 and expressed as 120 WO 2008/074821 PCT/EP2007/064185 percentage stimulation above basal. EC50 values were defined as the concentration of agonist required to give 50% of the maximal stimulation. Membrane preparation (alternative method) 5 For membrane preparations all steps were performed at 40C. Rat hepatoma cells stably expressing the human S1 P1 receptor or Rat Basophilic Leukaemia cells (RBL) stably expressing human S1 P3 receptor were grown to 80% confluency before being harvested into 10ml Phospho-Buffered Saline (PBS) and centrifuged at 1200rpm for 5 minutes. After removal of the supernatant, the pellet was re-suspended and cells 10 were homogenised within a glass Waring blender for 2 bursts of 15secs in 200mls of buffer (50mM HEPES, 1mM leupeptin, 25ptg/ml bacitracin, 1mM EDTA, 1mM PMSF, 2p.IM pepstatin A). The blender was plunged into ice for 5 mins after the first burst and 10-40 mins after the final burst to allow foam to dissipate. The material was then spun at 500g for 20 mins and the supernatant spun for 36 mins at 48,000g. The 15 pellet was resuspended in the same buffer as above but without PMSF and pepstatin A. The material was then forced through a 0.6mm needle, made up to the required volume, (usually x4 the volume of the original cell pellet), aliquoted and stored frozen at -800C. 20 S1 P1 GTPyS assay (alternative method) Human S1P1 rat hepatoma membranes (1.5p.g/well) were adhered to a wheatgerm agglutinin (WGA)-coated scintillation proximity assay (SPA) beads (0.125mg/well) in assay buffer (HEPES 20mM, MgCl 2 10mM, NaCl 100mM and pH adjusted to 7.4 using KOH 5M, GDP 10p.IM FAC (final assay concentration) and saponin 90p.g/ml 25 FAC was also added). After 30 minutes pre-coupling on ice the bead and membrane suspension was dispensed into a white Greiner polypropylene LV384-well plate (5p.l/well), containing 0.1pl of the compound. 5pLl/well [ 35 S]-GTPyS (0.5nM final radioligand conc) made up in assay buffer was then added to agonist plates. The final assay cocktail (10.1 I) 30 was then centrifuged at 1000rpm for 5 minutes then read immediately on a Viewlux reader. All test compounds were dissolved in DMSO at a concentration of 10mM and were prepared in 100% DMSO using a 1 in 4 dilution step to provide 11 point dose response curves. The dilutions were transferred to the assay plates ensuring that 35 the DMSO concentration was constant across the plate for all assays. 121 WO 2008/074821 PCT/EP2007/064185 All data was normalized to the mean of 16 high and 16 low control wells on each plate. A four parameter curve fit was then applied. Exemplified compounds of the invention that were tested in this assay had a pEC50 5 > 5. S11P3 S1P3 membranes from rat basophilic leukaemia cells (RBL-2H3)(1.5p.g/well) were adhered to WGA-coated SPA beads (0.125mg/well) in assay buffer (HEPES 20mM, 10 MgCl 2 3mM, NaCl 100mM and pH adjusted to 7.4 using KOH 5M), GDP 10p.M FAC and saponin 90p.g/ml FAC was also added). After 30 minutes pre-coupling on ice the bead and membrane suspension was dispensed into a white Greiner polypropylene LV384-well plate (5p.l/well), containing 0.1pl of the compound. 5pLl/well [ 35 S]-GTPyS (0.5nM final radioligand conc) made up 15 in assay buffer was then added to agonist plates. The final assay cocktail (10.1 I) was centrifuged at 1000rpm for 5 minutes then read immediately on a Viewlux reader. All test compounds were dissolved in DMSO at a concentration of 10mM and were prepared in 100% DMSO using a 1 in 4 dilution step to provide 11 point dose 20 response curves. The dilutions were transferred to the assay plates ensuring that the DMSO concentration was constant across the plate for all assays. All data was normalized to the mean of 16 high and 16 low control wells on each plate. A four parameter curve fit was then applied. 25 Exemplified compounds tested in this assay had a pEC50 < 6, many had a pEC50 <5. 30 Yeast assay Yeast (Saccharomyces cerevisiae) cells expressing the human S1 P1 receptor were generated by integration of an expression cassette into the ura3 chromosomal locus of yeast strain MMY23. This cassette consisted of DNA sequence encoding the human S1 P1 receptor flanked by the yeast GPD promoter to the 5' end of S1 P1 and 35 a yeast transcriptional terminator sequence to the 3' end of S1 P1. MMY23 expresses a yeast/mammalian chimeric G-protein alpha subunit in which the C-terminal 5 amino acids of Gpal are replaced with the C-terminal 5 amino acids of human Gail/2 (as described in Brown et al. (2000), Yeast 16:11-22). Cells were grown at 301C in liquid 122 CNRPonbI\DCC\RBR\4745014_i DOC-1511112012 Synthetic Complete (SC) yeast media (Guthrie and Fink (1991), Methods in Enzymology, Vol. 194) lacking uracil, tryptophan, adenine and leucine to late logarithmic phase (approximately 6 OD 600 lml). Agonists were prepared as 10 mM solutions in DMSO. EC 50 values (the concentration 5 required to produce 50% maximal response) were estimated using 4 fold dilutions (BiomekFX, Beckman) into DMSO. Agonist solutions in DMSO (1% final assay volume) were transferred into black microtitre plates from Greiner (384-well). Cells were suspended at a density of 0.2 OD 600 /ml in SC media lacking histidine, uracil, tryptophan, adenine and leucine and supplemented with 0.1mM 3-aminotriazole, 0.1M sodium 10 phosphate pH 7.0, and 10ptM fluorescein di-p-D-glucopyranoside (FDGlu). This mixture (50ul per well) was added to agonist in the assay plates (Multidrop 384, Labsystems). After incubation at 30 0 C for 24 hours, fluorescence resulting from degradation of FDGlu to fluorescein due to exoglucanase, an endogenous yeast enzyme produced during agonist stimulated cell growth, was determined using a fluorescence microtitre plate reader 15 (Tecan Spectrofluor or LJL Analyst excitation wavelength: 485nm; emission wavelength: 535nm). Fluorescence was plotted against compound concentration and iteratively curve fitted using a four parameter fit to generate a concentration effect value. Efficacy (Emax) was calculated from the equation Emax = Max[compound X] - Min[compound x] / Max[slp] - Min[swip x 100% 20 where Max[compound x, and Min[compound x, are the fitted maximum and minimum respectively from the concentration effect curve for compound X, and Max[sip and Mins 1 pi are the fitted maximum and minimum respectively from the concentration effect curve for Sphingosine-1 -Phosphate (available from Sigma). Equieffective molar ratio (EMR) values were calculated from the equation 25 EMR = EC 50 [compound x]/ EC 50 [sip Where EC 50 compound X) is the EC 50 of compound X and EC 50 [si is the EC 50 of S1P. Where tested, exemplified compounds of the invention had a pEC50 > 4.5 in the yeast assay. 30 The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from 123 C:WRPobl\DCC\RBR\4745014_i DOC-1511112012 it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates. Throughout this specification and the claims which follow, unless the context requires 5 otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. 124

Claims (7)

1. A compound of C1 0 _ CH 3 CH 3 N N N HO

4-[4-(5-{5-chloro-6-[(1 -methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1 H-indol-1 yl]butanoic acid and pharmaceutically acceptable salts thereof. 2. A compound according to claim 1 for use in the treatment of conditions or disorders mediated by S1 P1 receptors, wherein the condition or disorder is multiple sclerosis, autoimmune diseases, chronic inflammatory disorders, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, ulcerative colitis, lupus erythematosis, psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular diseases, pain conditions, acute viral diseases, inflammatory bowel conditions, insulin and non-insulin dependent diabetes. 3. A compound according to claim 2, wherein the condition is multiple sclerosis. 4. Use of a compound according to claim 1 in the manufacture a medicament for use in the treatment of conditions or disorders mediated by S1 P1 receptors, wherein the condition or disorder multiple sclerosis, autoimmune diseases, chronic inflammatory disorders, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, 125 C:\NRPortbl\DCC\FMT\4957274_1.DOC-27/02/2013 ulcerative colitis, lupus erythematosis, psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular diseases, pain conditions, acute viral diseases, inflammatory bowel conditions, insulin and non-insulin dependent diabetes.

5. Use according to claim 4, wherein the condition is multiple sclerosis.

6. A method for the treatment of conditions or disorders mediated by S1 P1 receptors comprising administering to the sufferer a therapeutically effective amount of a compound according to claim 1, wherein the condition or disorder multiple sclerosis, autoimmune diseases, chronic inflammatory disorders, asthma, inflammatory neuropathies, arthritis, transplantation, Crohn's disease, ulcerative colitis, lupus erythematosis, psoriasis, ischemia-reperfusion injury, solid tumours, and tumour metastasis, diseases associated with angiogenesis, vascular diseases, pain conditions, acute viral diseases, inflammatory bowel conditions, insulin and non-insulin dependent diabetes.

7. A method according to claim 6 wherein the condition is multiple sclerosis.

8. A pharmaceutical composition comprising a compound according to claim 1.

9. A compound according to claim 1 substantially as hereinbefore described with reference to any one of the Examples. 126