U.S. patent application number 12/820752 was filed with the patent office on 2010-10-14 for ep2 receptor agonists.
This patent application is currently assigned to Asterand UK Limited. Invention is credited to Mark Richard Ashton, Edward Andrew Boyd, Shirley Ann Brunton, David Edward Clark, Kenneth Lyle Clark, Robert Alexander Coleman, Richard John Davis, Garry Fenton, Neil Victor Harris, George Hynd, Alexander William Oxford, Keith Alfred James Stuttle, Jonathan Mark Sutton.
Application Number | 20100261760 12/820752 |
Document ID | / |
Family ID | 34890454 |
Filed Date | 2010-10-14 |
United States Patent
Application |
20100261760 |
Kind Code |
A1 |
Oxford; Alexander William ;
et al. |
October 14, 2010 |
EP2 Receptor Agonists
Abstract
The disclosure provides EP2 receptor agonist compounds and
methods for using the compounds for treating conditions which can
be alleviated by agonism of an EP2 receptor.
Inventors: |
Oxford; Alexander William;
(Royston, GB) ; Davis; Richard John; (Royston,
GB) ; Coleman; Robert Alexander; (Royston, GB)
; Clark; Kenneth Lyle; (Royston, GB) ; Clark;
David Edward; (Harlow, GB) ; Harris; Neil Victor;
(Harlow, GB) ; Fenton; Garry; (Harlow, GB)
; Hynd; George; (Harlow, GB) ; Stuttle; Keith
Alfred James; (Harlow, GB) ; Sutton; Jonathan
Mark; (Harlow, GB) ; Ashton; Mark Richard;
(Abingdon, GB) ; Boyd; Edward Andrew; (Abingdon,
GB) ; Brunton; Shirley Ann; (Abingdon, GB) |
Correspondence
Address: |
Jonathan P. O''Brien, Ph.D.;Honigman Miller Schwartz and Cohn
350 East Michigan Avenue, Suite 300
KALAMAZOO
MI
49007
US
|
Assignee: |
Asterand UK Limited
Royston
GB
|
Family ID: |
34890454 |
Appl. No.: |
12/820752 |
Filed: |
June 22, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12346516 |
Dec 30, 2008 |
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12820752 |
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11950613 |
Dec 5, 2007 |
7662839 |
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12346516 |
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11055724 |
Feb 11, 2005 |
7326732 |
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11950613 |
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60543538 |
Feb 12, 2004 |
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60626940 |
Nov 12, 2004 |
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Current U.S.
Class: |
514/340 ;
514/354; 514/448; 514/466; 514/471; 546/268.4; 546/323; 549/435;
549/487; 549/72 |
Current CPC
Class: |
C07D 277/56 20130101;
C07D 233/90 20130101; C07D 409/12 20130101; C07D 307/46 20130101;
C07D 401/12 20130101; A61P 19/08 20180101; C07D 405/12 20130101;
A61P 15/00 20180101; A61P 13/12 20180101; C07D 333/38 20130101;
C07C 235/84 20130101; C07D 277/26 20130101; C07D 213/81 20130101;
A61P 11/06 20180101; C07D 307/68 20130101; C07D 277/24 20130101;
A61P 27/06 20180101; A61P 37/00 20180101; C07D 405/04 20130101;
A61P 43/00 20180101; C07C 233/81 20130101; C07C 233/75 20130101;
C07D 257/04 20130101; A61P 19/10 20180101; C07D 307/91
20130101 |
Class at
Publication: |
514/340 ;
514/354; 514/448; 514/466; 514/471; 546/268.4; 546/323; 549/72;
549/435; 549/487 |
International
Class: |
A61K 31/4439 20060101
A61K031/4439; A61K 31/4418 20060101 A61K031/4418; A61K 31/381
20060101 A61K031/381; A61K 31/36 20060101 A61K031/36; A61K 31/341
20060101 A61K031/341; C07D 401/12 20060101 C07D401/12; C07D 213/81
20060101 C07D213/81; C07D 333/38 20060101 C07D333/38; C07D 407/10
20060101 C07D407/10; C07D 307/54 20060101 C07D307/54; A61P 13/12
20060101 A61P013/12; A61P 15/00 20060101 A61P015/00; A61P 27/06
20060101 A61P027/06; A61P 19/10 20060101 A61P019/10; A61P 11/06
20060101 A61P011/06; A61P 37/00 20060101 A61P037/00 |
Claims
1. A compound of formula (I): ##STR00391## or a salt, solvate and
chemically protected form thereof, wherein: R.sup.5 is an
optionally substituted C.sub.5-20 aryl or C.sub.4-20 alkyl group; A
is selected from the group consisting of: ##STR00392## wherein X
and Y are independently selected from the group consisting of: O
and CR.sup.3; S and CR.sup.3; NH and CR.sup.3; NH and N; O and N; S
and N; N and S; and N and O, and where the dotted lines indicate a
double bond in the appropriate location, and where Q is either N or
CH; R.sup.3 is selected from H, F, Cl and optionally substituted
C.sub.1-4 alkyl, C.sub.1-4 alkoxy, C.sub.5-7 aryl and C.sub.5-7
aryl-C.sub.1-4 alkyl groups; R.sup.4 is selected from H, F, Cl and
optionally substituted C.sub.1-4 alkyl, C.sub.1-4 alkoxy, C.sub.5-7
aryl and C.sub.5-7 aryl-C.sub.1-4 alkyl groups; R.sup.6 is selected
from H, F, Cl and optionally substituted C.sub.1-4 alkyl, C.sub.1-4
alkoxy, C.sub.5-7 aryl and C.sub.5-7 aryl-C.sub.1-4 alkyl groups; D
is selected from: ##STR00393## B is selected from the group
consisting of: ##STR00394## where R.sup.N' is selected from H and
C.sub.1-4 alkyl; where one of R.sup.P3 and R.sup.P4 is --C.sub.m
alkylene-R.sup.2 and the other of R.sup.P3 and R.sup.P4 is H, m and
n can be 0 or 1, and m+n=1 or 2; and additionally when R.sup.P3 is
--C.sub.m alkylene-R.sup.2, m can also be 2 or 3, and m+n=1, 2, 3
or 4, and when R.sup.2 is tetrazol-5-yl, m+n may be 0; or where one
of R.sup.P3 and R.sup.P4 is --O--CH.sub.2--R.sup.2, and the other
of R.sup.P3 and R.sup.P4 is H, n is 0; R.sup.N is H or optionally
substituted C.sub.1-4 alkyl; R.sup.2 is either: (i) --CO.sub.2H
(carboxy); (ii) --CONH.sub.2; (iii) --CH.sub.2--OH (methoxy); or
(iv) tetrazol-5-yl.
2. A compound according to claim 1, wherein R.sup.5 is phenyl
optionally substituted with one or more substituents independently
selected from: C.sub.1-4 alkyl, C.sub.1-4 alkoxy, C.sub.5-6 aryl,
halo, acyl, amino, alkoxylene.
3. A compound according to claim 1, wherein R.sup.5 is a C.sub.4-10
alkyl group.
4. A compound according to claim 1, wherein A is selected from:
##STR00395##
5. A compound according to claim 1, wherein A is a five membered
ring, and R.sup.3 (if present) and R.sup.4 are independently
selected from H and optionally substituted C.sub.1-4 alkyl.
6. A compound according to claim 1, wherein A is a six-membered
ring, and either: (i) R.sup.3, R.sup.4 and R.sup.6 (if present) are
H; or (ii) one of R.sup.3, R.sup.4 and R.sup.6 (if present) are Cl
or F.
7. A compound according to claim 1, wherein D is: ##STR00396##
8. A compound according to claim 7, wherein R.sup.N is H.
9. A compound according to claim 1, wherein B is: ##STR00397##
10. A compound according to claim 1, wherein R.sup.2 is carboxy or
tetrazoly-5-yl.
11. A compound according to claim 10, wherein R.sup.2 is
carboxy.
12. A compound according to claim 1, wherein R.sup.P4 is H, and
R.sup.P3 is --CH.dbd.CH--R.sup.2.
13. A compound according to claim 1, wherein R.sup.P3 is
--O--CH.sub.2--R.sup.2.
14. A pharmaceutical composition comprising a compound according to
claim 1, or a pharmaceutically acceptable salt thereof together
with a pharmaceutically acceptable carrier or diluent.
15. A method of treating a condition which can be alleviated by
agonism of an EP.sub.2 receptor, which method comprises
administering to a patient in need of treatment an effective amount
of a compound according to claim 1, or a pharmaceutically
acceptable salt thereof.
16. A method of treating a condition comprising administering to a
patient in need of treatment an effective amount of a compound
according to claim 1, or a pharmaceutically acceptable salt
thereof, wherein the condition is selected from dysmenorrhoea,
pre-term labour, glaucoma, ocular hypertension, immune disorders,
inflammatory disorders, osteoporosis, asthma, chronic obstructive
pulmonary disease, allergy, bone disease, fracture repair, male
sexual dysfunction, female sexual dysfunction, infertility,
periodontal disease, gastric ulcer, renal disease and psoriasis,
psoriatic arthritis, dermatitis, rheumatoid arthritis, transplant
rejection, inflammatory bowel disease, systemic lupus
erythematosus, vasculitis, acute respiratory distress syndrome,
pulmonary fibrosis, cystic fibrosis, Graves' disease, scleroderma,
multiple sclerosis, and type I diabetes.
17. The method of treating a condition according to claim 16
wherein the condition is selected from dysmenorrhoea, pre-term
labour, glaucoma, ocular hypertension, immune disorders,
inflammatory disorders, osteoporosis, asthma, chronic obstructive
pulmonary disease, allergy, bone disease, fracture repair, male
sexual dysfunction, female sexual dysfunction, infertility,
periodontal disease, gastric ulcer, renal disease and
psoriasis.
18. The method according to claim 16, wherein the condition is
glaucoma or ocular hypertension.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of application Ser. No.
12/346,516, filed Dec. 30, 2008, which is a divisional of
application Ser. No. 11/950,613, filed Dec. 5, 2007, now U.S. Pat.
No. 7,662,839 which application is a divisional of application Ser.
No. 11/055,724, filed Feb. 11, 2005, now U.S. Pat. No. 7,326,732,
which claims benefit of U.S. Provisional Application Nos.
60/626,940, filed Nov. 12, 2004, and 60/543,538, filed Feb. 12,
2004; the entire contents of each which are hereby incorporated by
reference in this application.
[0002] This invention relates to EP.sub.2 receptor agonists,
pharmaceutical compositions comprising such compounds, and the use
of such compounds and compositions to treat various diseases.
BACKGROUND TO THE INVENTION
[0003] Prostanoids comprise prostaglandins (PGs) and thromboxanes
(Txs) and their receptors fall into five different classes (DP, EP,
FP, IP and TP) based on their sensitivity to the five naturally
occurring prostanoids, PGD.sub.2, PGE.sub.2, PGF.sub.2.alpha.,
PGI.sub.2 and TxA.sub.2, respectively (Coleman, R. A., Prostanoid
Receptors. IUPHAR compendium of receptor characterisation and
classification, 2.sup.nd edition, 338-353, ISBN 0-9533510-3-3,
2000). EP receptors (for which the endogenous ligand is PGE.sub.2)
have been subdivided into four types termed EP.sub.1, EP.sub.2,
EP.sub.3 and EP.sub.4. These four types of EP receptors have been
cloned and are distinct at both a molecular and pharmacological
level (Coleman, R. A., 2000)
[0004] EP.sub.2 agonists have been shown to be effective in the
treatment of a number of conditions, including (but not limited to)
dysmenorrhoea (WO 03/037433), pre-term labour (GB 2 293 101),
glaucoma (WO 03/040126), ocular hypertension (WO 03/040126), immune
disorders (Nataraj, C., et al., J. Clin. Invest., 108, 1229-1235
(2001)), osteoporosis (WO 98/27976, WO 01/46140), asthma (Tilley,
et al., Am. J. Physiol. Lung Cell Mol. Physiol., 284, L599-606
(2003)), allergy, bone disease (WO 02/24647), fracture repair (WO
98/27976, WO 02/24647), male sexual dysfunction (WO 00/40248),
female sexual dysfunction (U.S. Pat. No. 6,562,868), periodontal
disease (WO 00/31084), gastric ulcer (U.S. Pat. No. 5,576,347) and
renal disease (WO 98/34916).
[0005] In co-pending applications GB 0329620.9, filed 22 Dec. 2003
and a corresponding US provisional application filed 24 Dec. 2003,
which are hereby incorporated by reference, it has been shown that
EP.sub.2 agonists inhibit lymphocyte activation and the release of
pro-inflammatory cytokines from alveolar macrophages. In addition,
EP.sub.2 activation inhibits monocyte and neutrophil activation.
Thus, EP.sub.2 agonists should prove useful in the treatment of
inflammatory and immune disorders such as psoriasis, dermatitis,
rheumatoid arthritis, multiple sclerosis, scleroderma, transplant
rejection, allergy, systemic lupus erythematosus, vasculitis, type
1 diabetes mellitus, and inflammatory lung diseases such as chronic
obstructive pulmonary disease, asthma, acute respiratory distress
syndrome and cystic fibrosis.
[0006] In addition, EP.sub.2 agonists can also be used in the
treatment of fibrosis, including, but not limited to idiopathic
pulmonary fibrosis, scleroderma and systemic sclerosis,
post-operative fibrosis following trabulectomy, liver repair and
regeneration following cirrhosis, hepatitis, toxicity, cancer or
renal fibrosis. EP.sub.2 agonists can also be used in the
prevention of fibroblast to myofibroblast conversion to treat
asthma and other fibrotic lung diseases. EP.sub.2 agonists may also
be used to maintain ductus arteriosus patency in infants with
congenital heart disease.
[0007] Compounds which combine EP.sub.2 receptor agonist and EP,
receptor antagonist properties may prove useful in the treatment of
several diseases including myometrial disorders, bone diseases
including osteoporosis and osteoarthritis, allergic and immune
disorders such as psoriasis, transplant rejection, and asthma,
inflammatory diseases such as rheumatoid arthritis, chronic
obstructive pulmonary disease and acute respiratory disease
syndrome, and fibrotic lung diseases.
SUMMARY OF THE INVENTION
[0008] A first aspect of the present invention provides a compound
of formula (I):
##STR00001##
or a salt, solvate and chemically protected form thereof, wherein:
R.sup.5 is an optionally substituted C.sub.5-20 aryl or C.sub.4-20
alkyl group; A is selected from the group consisting of:
##STR00002##
wherein X and Y are selected from the group consisting of: O and
CR.sup.3; S and CR.sup.3; NH and CR.sup.3; NH and N; O and N; S and
N; N and S; and N and O, and where the dotted lines indicate a
double bond in the appropriate location, and where Q is either N or
CH; R.sup.3 is selected from H, F, Cl and optionally substituted
C.sub.1-4 alkyl, C.sub.1-4 alkoxy, C.sub.5-7 aryl and C.sub.5-7
aryl-C.sub.1-4 alkyl groups; R.sup.4 is selected from H, F, Cl and
optionally substituted C.sub.1-4 alkyl, C.sub.1-4 alkoxy, C.sub.5-7
aryl and C.sub.5-7 aryl-C.sub.1-4 alkyl groups; R.sup.6 is selected
from H, F, Cl and optionally substituted C.sub.1-4 alkyl, C.sub.1-4
alkoxy, C.sub.5-7 aryl and C.sub.5-7 aryl-C.sub.1-4 alkyl groups; D
is selected from:
##STR00003##
B is selected from the group consisting of:
##STR00004##
where R.sup.N' is selected from H and C.sub.1-4 alkyl; where one of
R.sup.P3 and R.sup.P4 is --C.sub.m alkylene-R.sup.2 and the other
of R.sup.P3 and R.sup.P4 is H, m and n can be 0 or 1, and m+n=1 or
2; and additionally when R.sup.P3 is --C.sub.m alkylene-R.sup.2, m
can also be 2 or 3, and m+n=1, 2, 3 or 4, and when R.sup.2 is
tetrazol-5-yl, m+n may be 0; or where one of R.sup.P3 and R.sup.P4
is --O--CH.sub.2--R.sup.2, and the other of R.sup.P3 and R.sup.P4
is H, n is 0; R.sup.N is H or optionally substituted C.sub.1-4
alkyl; R.sup.2 is either: (i) --CO.sub.2H (carboxy);
(ii) --CONH.sub.2;
[0009] (iii) --CH.sub.2--OH (methoxy); or (iv) tetrazol-5-yl.
[0010] Therefore, A may be one of the following groups:
##STR00005##
[0011] A second aspect of the present invention provides a compound
of formula (I) or a pharmaceutically acceptable salt thereof for
use in a method of therapy.
[0012] A third aspect of the present invention provides a
pharmaceutical composition comprising a compound of formula (I) as
defined in the first aspect or a pharmaceutically acceptable salt
thereof together with a pharmaceutically acceptable carrier or
diluent.
[0013] A fourth aspect of the present invention provides the use of
a compound of formula (I) or a pharmaceutically acceptable salt
thereof in the preparation of a medicament for the treatment of a
condition alleviated by agonism of an EP.sub.2 receptor.
[0014] A fifth aspect of the present invention provides a method of
treating a condition which can be alleviated by agonism of an
EP.sub.2 receptor, which method comprises administering to a
patient in need of treatment an effective amount of a compound of
formula (I), or a pharmaceutically acceptable salt thereof.
[0015] In the fourth and fifth aspects of the invention, the
agonism of the EP.sub.2 receptor may be selective, or may be
accompanied by antagonism of the EP.sub.4 receptor.
[0016] Conditions which can be alleviated by agonism of an EP.sub.2
receptor are discussed above, and particularly include
dysmenorrhoea, pre-term labour, glaucoma, ocular hypertension,
immune disorders, inflammatory disorders, osteoporosis, asthma,
chronic obstructive pulmonary disease, allergy, bone disease,
fracture repair, male sexual dysfunction, female sexual
dysfunction, infertility, periodontal disease, gastric ulcer, renal
disease and psoriasis.
[0017] Conditions which can be alleviated by combined agonism of
EP.sub.2 receptors and antagonism of EP, receptors are discussed
above, and particularly include myometrial disorders, bone diseases
including osteoporosis and osteoarthritis, allergic and immune
disorders such as psoriasis, transplant rejection, and asthma,
inflammatory diseases such as rheumatoid arthritis, chronic
obstructive pulmonary disease and acute respiratory disease
syndrome, and fibrotic lung diseases.
[0018] EP receptor agonists are known to be able to inhibit T-cell
activation and the release of pro-inflammatory cytokines, although
the EP receptor involved in mediating these effects in human
T-cells has not been previously defined. Some of the present
inventors have discovered that EP.sub.2 agonists inhibit human
T-cell activation (proliferation) and inhibit the release of
multiple pro-inflammatory cytokines including interleukin 2 (IL-2)
tumour necrosis factor (TNF.sub..alpha.) and interferon gamma
(IFN.gamma.), as described in co-pending US and International
applications entitled "EP.sub.2 Agonists" filed 22 Dec. 2004 in the
name of Borman, R. A. et al., (PCT/GB2004/005421), which are herein
incorporated by reference. This profile of activity strongly
suggests that EP.sub.2 receptor agonists will be useful in treating
immune and inflammatory disorders, including but not limited to
psoriasis, psoriatic arthritis, dermatitis, rheumatoid arthritis,
transplant rejection, inflammatory bowel disease, systemic lupus
erythematosus, Graves' disease, scleroderma, multiple sclerosis,
Type I diabetes, and transplant rejection, and in particular
psoriasis (Griffiths, C., Current Drugs Targets--Inflammation &
Allergy, 3, 157-161, (2004); Lebwohl, M., Lancet, 361, 1197-1204
(2003); Salim, A. & Emerson, R., Curr. Opin. Investig. Drugs,
2(11), 1546-8 (2001)). Therefore, a further condition which can be
alleviated by agonism of an EP.sub.2 receptor is psoriasis.
[0019] Furthermore, some of the present inventors have also shown
that EP.sub.2 receptor agonists inhibit the release of the
pro-inflammatory cytokine, TNF.sub..alpha. from human monocytes and
alveolar macrophages, as described in co-pending US and
International applications entitled "EP.sub.2 Agonists" filed 22
Dec. 2004 in the name of Borman, R. A. et al., (PCT/GB2004/005421),
which are herein incorporated by reference. This profile of
activity adds further evidence to the view that that EP.sub.2
receptor agonists will be useful in treating immune and
inflammatory disorders and in particular, inflammatory lung
diseases (including, but not limited to: asthma, chronic
obstructive pulmonary disease, acute respiratory distress syndrome,
pulmonary fibrosis and cystic fibrosis).
[0020] Furthermore, aspects of the present invention relate to the
use of EP.sub.2 agonists to treat conditions ameliorated by the
inhibition of IL-2 TNF.sub..alpha. and/or IFN.gamma. production and
the use of an EP.sub.2 agonist in the preparation of a medicament
for the treatment of a condition alleviated by inhibition of IL-2
production.
[0021] The present invention also provides methods of stimulating
EP.sub.2 receptors and/or inhibiting the production of IL-2,
TNF.sub..alpha. and/or IFN.gamma., in vitro or in vivo, comprising
contacting a cell with an effective amount of a compound of the
first aspect of the present invention.
[0022] Compounds of the present invention can be assayed to
determine whether they act as antagonists of an EP, receptor.
Suitable assay methods are described in example 6 below.
[0023] The present invention also provides methods of agonising
EP.sub.2, and possible antagonizing EP.sub.4 receptors, in vitro or
in vivo, comprising contacting a cell with an effective amount of a
compound of formula (I).
[0024] In some embodiments, the compounds described above which
function as EP.sub.2 agonists may be selective as against
modulation of one or more of the other three EP receptors, i.e.
EP.sub.1, EP.sub.3 and EP.sub.4. This selectivity allows for
targeting of the effect of the compounds of the invention, with
possible benefits in the treatment of certain conditions.
DEFINITIONS
Monodentate Groups
[0025] (I.e Groups with One Point of Covalent Attachment)
[0026] Alkyl: The term "alkyl" as used herein, pertains to a
monovalent moiety obtained by removing a hydrogen atom from a
carbon atom of a hydrocarbon compound having from 1 to 20 carbon
atoms (unless otherwise specified), which may be aliphatic or
alicyclic, and which may be saturated or unsaturated. Thus, the
term "alkyl" includes the sub-classes alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, cylcoalkynyl, etc., discussed below.
[0027] In the context of alkyl groups, the prefixes (e.g.
C.sub.1-4, C.sub.1-7, C.sub.1-20, C.sub.2-7, C.sub.3-7) denote the
number of carbon atoms, or range of number of carbon atoms. For
example, the term "C.sub.1-4 alkyl" as used herein, pertains to an
alkyl group having from 1 to 4 carbon atoms. Examples of groups of
alkyl groups include C.sub.1-4 alkyl ("lower alkyl"), C.sub.1-7
alkyl and C.sub.4-20 alkyl. Note that the first prefix may vary
according to other limitations; for example, for unsaturated alkyl
groups, the first prefix must be at least 2; for cyclic alkyl
groups, the first prefix must be at least 3; etc.
[0028] Examples of saturated alkyl groups include, but are not
limited to, methyl (C.sub.1), ethyl (C.sub.2), propyl (C.sub.3),
butyl (C.sub.4), pentyl (C.sub.5), hexyl (C.sub.6), heptyl
(C.sub.7), octyl (C.sub.8), nonyl (C.sub.9), decyl (C.sub.10),
undecyl (C.sub.11), dodecyl (C.sub.12), tridecyl (C.sub.13),
tetradecyl (C.sub.14), pentadecyl (C.sub.15), and eicodecyl
(C.sub.20).
[0029] Examples of saturated linear alkyl groups include, but are
not limited to, methyl (C.sub.1), ethyl (C.sub.2), n-propyl
(C.sub.3), n-butyl (C.sub.4), n-pentyl (amyl) (C.sub.5), n-hexyl
(C.sub.6), and n-heptyl (C.sub.7).
[0030] Examples of saturated branched alkyl groups include
iso-propyl (C.sub.3), iso-butyl (C.sub.4), sec-butyl (C.sub.4),
tert-butyl (C.sub.4), iso-pentyl (C.sub.5), and neo-pentyl
(C.sub.5).
[0031] Alkenyl: The term "alkenyl" as used herein, pertains to an
alkyl group having one or more carbon-carbon double bonds. Examples
of alkenyl groups include C.sub.2-4 alkenyl, C.sub.2-7 alkenyl and
C.sub.2-20alkenyl. Examples of alkenyl groups include, but are not
limited to, ethenyl (vinyl, --CH.dbd.CH.sub.2), 1-propenyl
(--CH.dbd.CH--CH.sub.3), 2-propenyl (allyl, --CH--CH.dbd.CH.sub.2),
isopropenyl (1-methylvinyl, --C(CH.sub.3).dbd.CH.sub.2), butenyl
(C.sub.4), pentenyl (C.sub.5), and hexenyl (C.sub.6).
[0032] Alkynyl: The term "alkynyl" as used herein, pertains to an
alkyl group having one or more carbon-carbon triple bonds. Examples
of groups of alkynyl groups include C.sub.2-4 alkynyl, C.sub.2-7
alkynyl and C.sub.2-20 alkynyl. Examples of alkynyl groups include,
but are not limited to, ethynyl (ethinyl, --C.ident.CH) and
2-propynyl (propargyl, --CH.sub.2--C.ident.CH).
[0033] Cycloalkyl: The term "cycloalkyl" as used herein, pertains
to an alkyl group which is also a cyclyl group; that is, a
monovalent moiety obtained by removing a hydrogen atom from an
alicyclic ring atom of a carbocyclic ring of a carbocyclic
compound, which carbocyclic ring may be saturated or unsaturated,
which moiety has from 3 to 7 carbon atoms (unless otherwise
specified), including from 3 to 7 ring atoms. Thus, the term
"cycloalkyl" includes the sub-classes cycloalkenyl and
cycloalkynyl. Preferably, each ring has from 3 to 7 ring atoms.
Examples of groups of cycloalkyl groups include C.sub.3-7
cycloalkyl.
[0034] Examples of cycloalkyl groups include, but are not limited
to, those derived from: [0035] saturated monocyclic hydrocarbon
compounds: cyclopropane (C.sub.3), cyclobutane (C.sub.4),
cyclopentane (C.sub.5), cyclohexane (C.sub.6), cycloheptane
(C.sub.7), methylcyclopropane (C.sub.4), dimethylcyclopropane
(C.sub.5), methylcyclobutane (C.sub.5), dimethylcyclobutane
(C.sub.6), methylcyclopentane (C.sub.6), dimethylcyclopentane
(C.sub.7), methylcyclohexane (C.sub.7) dimethylcyclohexene
(C.sub.8), menthane (C.sub.10); [0036] unsaturated monocyclic
hydrocarbon compounds: cyclopropene (C.sub.3), cyclobutene
(C.sub.4), cyclopentene (C.sub.5), cyclohexene (C.sub.6),
methylcyclopropene (C.sub.4), dimethylcyclopropene (C.sub.5),
methylcyclobutene (C.sub.5), dimethylcyclobutene (C.sub.6),
methylcyclopentene (C.sub.6), dimethylcyclopentene (C.sub.7),
methylcyclohexene (C.sub.7) dimethylcyclohexene (C.sub.8); [0037]
saturated polycyclic hydrocarbon compounds: thujane (C.sub.10),
carane (C.sub.10), pinane (C.sub.10), bornane (C.sub.10), norcarane
(C.sub.7), norpinane (C.sub.7), norbornane (C.sub.7), adamantane
(C.sub.10), decalin (decahydronaphthalene) (C.sub.10); [0038]
unsaturated polycyclic hydrocarbon compounds: camphene (C.sub.10),
limonene (C.sub.10), pinene (C.sub.10).
[0039] Heterocyclyl: The term "heterocyclyl" as used herein,
pertains to a monovalent moiety obtained by removing a hydrogen
atom from a ring atom of a heterocyclic compound, which moiety has
from 3 to 20 ring atoms (unless otherwise specified), of which from
1 to 10 are ring heteroatoms. Preferably, each ring has from 3 to 7
ring atoms, of which from 1 to 4 are ring heteroatoms.
[0040] In this context, the prefixes (e.g. C.sub.3-20, C.sub.3-7,
C.sub.5-6, etc.) denote the number of ring atoms, or range of
number of ring atoms, whether carbon atoms or heteroatoms. For
example, the term "C.sub.5-6 heterocyclyl" as used herein, pertains
to a heterocyclyl group having 5 or 6 ring atoms. Examples of
groups of heterocyclyl groups include C.sub.3-20 heterocyclyl,
C.sub.5-20 heterocyclyl, C.sub.3-15 heterocyclyl, C.sub.5-15
heterocyclyl, C.sub.3-12 heterocyclyl, C.sub.5-12 heterocyclyl,
C.sub.3-10 heterocyclyl, C.sub.5-10 heterocyclyl, C.sub.3-7
heterocyclyl, C.sub.5-7 heterocyclyl, and C.sub.5-6
heterocyclyl.
[0041] Examples of monocyclic heterocyclyl groups include, but are
not limited to, those derived from:
N.sub.1: aziridine (C.sub.3), azetidine (C.sub.4), pyrrolidine
(tetrahydropyrrole) (C.sub.5), pyrroline (e.g., 3-pyrroline,
2,5-dihydropyrrole) (C.sub.5), 2H-pyrrole or 3H-pyrrole
(isopyrrole, isoazole) (C.sub.5), piperidine (C.sub.6),
dihydropyridine (C.sub.6), tetrahydropyridine (C.sub.6), azepine
(C.sub.7); O.sub.1: oxirane (C.sub.3), oxetane (C.sub.4), oxolane
(tetrahydrofuran) (C.sub.5), oxole (dihydrofuran) (C.sub.5), oxane
(tetrahydropyran) (C.sub.6), dihydropyran (C.sub.6), pyran
(C.sub.6), oxepin (C.sub.7); S.sub.1: thiirane (C.sub.3), thietane
(C.sub.4), thiolane (tetrahydrothiophene) (C.sub.5), thiane
(tetrahydrothiopyran) (C.sub.6), thiepane (C.sub.7); O.sub.2:
dioxolane (C.sub.5), dioxane (C.sub.6), and dioxepane (C.sub.7);
O.sub.3: trioxane (C.sub.6); N.sub.2: imidazolidine (C.sub.5),
pyrazolidine (diazolidine) (C.sub.5), imidazoline (C.sub.5),
pyrazoline (dihydropyrazole) (C.sub.5), piperazine (C.sub.6);
N.sub.1O.sub.1: tetrahydrooxazole (C.sub.5), dihydrooxazole
(C.sub.5), tetrahydroisoxazole (C.sub.5), dihydroisoxazole
(C.sub.5), morpholine (C.sub.6), tetrahydrooxazine (C.sub.6),
dihydrooxazine (C.sub.6), oxazine (C.sub.6); N.sub.1S.sub.1:
thiazoline (C.sub.5), thiazolidine (C.sub.5), thiomorpholine
(C.sub.6); N.sub.2O.sub.1: oxadiazine (C.sub.6); O.sub.1S.sub.1:
oxathiole (C.sub.5) and oxathiane (thioxane) (C.sub.6); and,
N.sub.1O.sub.1S.sub.1: oxathiazine (C.sub.6).
[0042] Aryl: The term "aryl" as used herein, pertains to a
monovalent moiety obtained by removing a hydrogen atom from an
aromatic ring atom of an aromatic compound, which moiety has from 3
to 20 ring atoms (unless otherwise specified). Preferably, each
ring has from 5 to 7 ring atoms.
[0043] In this context, the prefixes (e.g. C.sub.3-20, C.sub.5-7,
C.sub.5-6, etc.) denote the number of ring atoms, or range of
number of ring atoms, whether carbon atoms or heteroatoms. For
example, the term "C.sub.5-6 aryl" as used herein, pertains to an
aryl group having 5 or 6 ring atoms. Examples of groups of aryl
groups include C.sub.3-20 aryl, C.sub.5-20 aryl, C.sub.5-15 aryl,
C.sub.5-12 aryl, C.sub.5-10 aryl, C.sub.5-7 aryl, C.sub.5-6 aryl,
C.sub.5 aryl, and C.sub.6 aryl.
[0044] The ring atoms may be all carbon atoms, as in "carboaryl
groups". Examples of carboaryl groups include C.sub.3-20 carboaryl,
C.sub.5-20 carboaryl, C.sub.5-15 carboaryl, C.sub.5-12 carboaryl,
C.sub.5-10 carboaryl, C.sub.5-7 carboaryl, C.sub.5-6 carboaryl,
C.sub.5 carboaryl, and C.sub.6 carboaryl.
[0045] Examples of carboaryl groups include, but are not limited
to, those derived from benzene (i.e. phenyl) (C.sub.6), naphthalene
(C.sub.10), azulene (C.sub.10), anthracene (C.sub.14), phenanthrene
(C.sub.14), naphthacene (C.sub.18), and pyrene (C.sub.16).
[0046] Examples of aryl groups which comprise fused rings, at least
one of which is an aromatic ring, include, but are not limited to,
groups derived from indane (e.g., 2,3-dihydro-1H-indene) (C.sub.9),
indene (C.sub.9), isoindene (C.sub.9), tetraline
(1,2,3,4-tetrahydronaphthalene (C.sub.10), acenaphthene (C.sub.12),
fluorene (C.sub.13), phenalene (C.sub.13), acephenanthrene
(C.sub.15), and aceanthrene (C.sub.16).
[0047] Alternatively, the ring atoms may include one or more
heteroatoms, as in "heteroaryl groups". Examples of heteroaryl
groups include C.sub.3-20 heteroaryl, C.sub.5-20 heteroaryl,
C.sub.5-15 heteroaryl, C.sub.5-12 heteroaryl, C.sub.5-10
heteroaryl, C.sub.5-7 heteroaryl, C.sub.5-6 heteroaryl, C.sub.5
heteroaryl, and C.sub.6 heteroaryl.
[0048] Examples of monocyclic heteroaryl groups include, but are
not limited to, those derived from:
N.sub.1: pyrrole (azole) (C.sub.5), pyridine (azine) (C.sub.6);
O.sub.1: furan (oxole) (C.sub.5); S.sub.1: thiophene (thiole)
(C.sub.5); N.sub.1O.sub.1: oxazole (C.sub.5), isoxazole (C.sub.5),
isoxazine (C.sub.6); N.sub.2O.sub.1: oxadiazole (furazan)
(C.sub.5); N.sub.3O.sub.1: oxatriazole (C.sub.5); N.sub.1S.sub.1:
thiazole (C.sub.5), isothiazole (C.sub.5); N.sub.2: imidazole
(1,3-diazole) (C.sub.5), pyrazole (1,2-diazole) (C.sub.5),
pyridazine (1,2-diazine) (C.sub.6), pyrimidine (1,3-diazine)
(C.sub.6), pyrazine (1,4-diazine) (C.sub.6); N.sub.3: triazole
(C.sub.5), triazine (C.sub.6); and, N.sub.4: tetrazole
(C.sub.5).
[0049] Examples of heteroaryl groups which comprise fused rings,
include, but are not limited to: [0050] C.sub.9 (with 2 fused
rings) derived from benzofuran (O.sub.1), isobenzofuran (O.sub.1),
indole (N.sub.1), isoindole (N.sub.1), indolizine (N.sub.1),
indoline (N.sub.1), isoindoline (N.sub.1), purine (N.sub.4) (e.g.,
adenine, guanine), benzimidazole (N.sub.2), indazole (N.sub.2),
benzoxazole (N.sub.1O.sub.1), benzisoxazole (N.sub.3O.sub.1),
benzodioxole (O.sub.2), benzofurazan (N.sub.2O.sub.1),
benzotriazole (N.sub.3), benzothiofuran (S.sub.1), benzothiazole
(N.sub.1S.sub.2), benzothiadiazole (N.sub.2S); [0051] C.sub.10
(with 2 fused rings) derived from chromene (O.sub.2), isochromene
(O.sub.1), chroman (O.sub.1), isochroman (O.sub.1), benzodioxan
(O.sub.2), quinoline (N.sub.1), isoquinoline (N.sub.1), quinolizine
(N.sub.1), benzoxazine (N.sub.1O.sub.1), benzodiazine (N.sub.2),
pyridopyridine (N.sub.2), quinoxaline (N.sub.2), quinazoline
(N.sub.2), cinnoline (N.sub.2), phthalazine (N.sub.2),
naphthyridine (N.sub.2), pteridine (N.sub.4); [0052] C.sub.11 (with
2 fused rings) derived from benzodiazepine (N.sub.2); [0053]
C.sub.13 (with 3 fused rings) derived from carbazole (N.sub.1),
dibenzofuran (O.sub.1), dibenzothiophene (S.sub.1), carboline
(N.sub.2), perimidine (N.sub.2), pyridoindole (N.sub.2); and,
[0054] C.sub.14 (with 3 fused rings) derived from acridine
(N.sub.1), xanthene (O.sub.1), thioxanthene (S.sub.1), oxanthrene
(O.sub.2), phenoxathiin (O.sub.1S.sub.1), phenazine (N.sub.2),
phenoxazine (N.sub.2O.sub.1), phenothiazine (N.sub.1S.sub.1),
thianthrene (S.sub.2), phenanthridine (N.sub.1), phenanthroline
(N.sub.2), phenazine (N.sub.2).
[0055] If a heteroaryl or heterocyclyl group contains a nitrogen
ring atom, this ring atom, where possible, may be in a oxidised
state, as an N-oxide.
[0056] The above groups, whether alone or part of another
substituent, may themselves optionally be substituted with one or
more groups selected from themselves, the additional monodentate
substituents listed below and alkoxylene.
[0057] Halo: --F, --Cl, --Br, and --I.
[0058] Hydroxy: --OH.
[0059] Ether: --OR, wherein R is an ether substituent, for example,
a C.sub.1-7 alkyl group (also referred to as a C.sub.1-7 alkoxy
group, discussed below), a C.sub.3-20 heterocyclyl group (also
referred to as a C.sub.3-20 heterocyclyloxy group), or a C.sub.5-20
aryl group (also referred to as a C.sub.5-20 aryloxy group),
preferably a C.sub.1-7 alkyl group.
[0060] C.sub.1-7 alkoxy: --OR, wherein R is a C.sub.1-7 alkyl
group. Examples of C.sub.1-7 alkoxy groups include, but are not
limited to, --OMe (methoxy), --OEt (ethoxy), --O(nPr) (n-propoxy),
--O(iPr) (isopropoxy), --O(nBu) (n-butoxy), --O(sBu) (sec-butoxy),
--O(iBu) (isobutoxy), and --O(tBu) (tert-butoxy).
[0061] Oxo (keto, -one): .dbd.O.
[0062] Thione (thioketone): .dbd.S.
[0063] Imino (imine): .dbd.NR, wherein R is an imino substituent,
for example, hydrogen, C.sub.1-7 alkyl group, a C.sub.3-20
heterocyclyl group, or a C.sub.5-20 aryl group, preferably hydrogen
or a C.sub.1-7 alkyl group. Examples of imino groups include, but
are not limited to, .dbd.NH, .dbd.NMe, .dbd.NEt, and .dbd.NPh.
[0064] Formyl (carbaldehyde, carboxaldehyde): --C(.dbd.O)H.
[0065] Acyl (keto): --C(.dbd.O)R, wherein R is an acyl substituent,
for example, a C.sub.1-7 alkyl group (also referred to as C.sub.1-7
alkylacyl or C.sub.1-7 alkanoyl), a C.sub.3-20 heterocyclyl group
(also referred to as C.sub.3-20 heterocyclylacyl), or a C.sub.5-20
aryl group (also referred to as C.sub.5-20 arylacyl), preferably a
C.sub.1-7 alkyl group. Examples of acyl groups include, but are not
limited to, --C(.dbd.O)CH.sub.3 (acetyl),
--C(.dbd.O)CH.sub.2CH.sub.3 (propionyl),
--C(.dbd.O)C(CH.sub.3).sub.3 (t-butyryl), and --C(.dbd.O)Ph
(benzoyl, phenone).
[0066] Carboxy (carboxylic acid): --C(.dbd.O)OH.
[0067] Thiocarboxy (thiocarboxylic acid): --C(.dbd.S)SH.
[0068] Thiolocarboxy (thiolocarboxylic acid): --C(.dbd.O)SH.
[0069] Thionocarboxy (thionocarboxylic acid): --C(.dbd.S)OH.
[0070] Imidic acid: --C(.dbd.NH)OH.
[0071] Hydroxamic acid: --C(.dbd.NOH)OH.
[0072] Ester (carboxylate, carboxylic acid ester, oxycarbonyl):
--C(.dbd.O)OR, wherein R is an ester substituent, for example, a
C.sub.1-7 alkyl group, a C.sub.3-20 heterocyclyl group, or a
C.sub.5-20 aryl group, preferably a C.sub.1-7 alkyl group. Examples
of ester groups include, but are not limited to,
--C(.dbd.O)OCH.sub.3, --C(.dbd.O)OCH.sub.2CH.sub.3,
--C(.dbd.O)OC(CH.sub.3).sub.3, and --C(.dbd.O)OPh.
[0073] Acyloxy (reverse ester): --OC(.dbd.O)R, wherein R is an
acyloxy substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably a C.sub.1-7 alkyl group. Examples of acyloxy groups
include, but are not limited to, --OC(.dbd.O)CH.sub.3 (acetoxy),
--OC(.dbd.O)CH.sub.2CH.sub.3, --OC(.dbd.O)C(CH.sub.3).sub.3,
--OC(.dbd.O)Ph, and --OC(.dbd.O)CH.sub.2Ph.
[0074] Amido (carbamoyl, carbamyl, aminocarbonyl, carboxamide):
--C(.dbd.O)NR.sup.1R.sup.2, wherein R.sup.1 and R.sup.2 are
independently amino substituents, as defined for amino groups.
Examples of amido groups include, but are not limited to,
--C(.dbd.O)NH.sub.2, --C(.dbd.O)NHCH.sub.3,
--C(.dbd.O)N(CH.sub.3).sub.2, --C(.dbd.O)NHCH.sub.2CH.sub.3, and
--C(.dbd.O)N(CH.sub.2CH.sub.3).sub.2, as well as amido groups in
which R.sup.1 and R.sup.2, together with the nitrogen atom to which
they are attached, form a heterocyclic structure as in, for
example, piperidinocarbonyl, morpholinocarbonyl,
thiomorpholinocarbonyl, and piperazinocarbonyl.
[0075] Acylamino: --NR.sup.1C(.dbd.O)R.sup.2, wherein R.sup.1 is an
amide substituent, for example, hydrogen, a C.sub.1-7 alkyl group,
a C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably hydrogen or a C.sub.1-7 alkyl group, and R.sup.2 is an
acyl substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably hydrogen or a C.sub.1-7 alkyl group. Examples of
acylamide groups include, but are not limited to,
--NHC(.dbd.O)CH.sub.3, --NHC(.dbd.O)CH.sub.2CH.sub.3, and
--NHC(.dbd.O)Ph. R.sup.1 and R.sup.2 may together form a cyclic
structure, as in, for example, succinimidyl, maleimidyl, and
phthalimidyl:
##STR00006##
[0076] Thioamido (thiocarbamyl): --C(.dbd.S)NR.sup.1R.sup.2,
wherein R.sup.1 and R.sup.2 are independently amino substituents,
as defined for amino groups. Examples of thioamido groups include,
but are not limited to, --C(.dbd.S)NH.sub.2, --C(.dbd.S)NHCH.sub.3,
--C(.dbd.S)N(CH.sub.3).sub.2, and
--C(.dbd.S)NHCH.sub.2CH.sub.3.
[0077] Ureido: --N(R.sup.1)CONR.sup.2R.sup.3 wherein R.sup.2 and
R.sup.3 are independently amino substituents, as defined for amino
groups, and R.sup.1 is a ureido substituent, for example, hydrogen,
a C.sub.1-7 alkyl group, a C.sub.3-20 heterocyclyl group, or a
C.sub.5-20 aryl group, preferably hydrogen or a C.sub.1-7 alkyl
group. Examples of ureido groups include, but are not limited to,
--NHCONH.sub.2, --NHCONHMe, --NHCONHEt, --NHCONMe.sub.2,
--NHCONEt.sub.2, --NMeCONH.sub.2, --NMeCONHMe, --NMeCONHEt,
--NMeCONMe.sub.2, and --NMeCONEt.sub.2.
[0078] Guanidino: --NH--C(.dbd.NH)NH.sub.2.
[0079] Tetrazolyl: a five membered aromatic ring having four
nitrogen atoms and one carbon atom,
##STR00007##
[0080] Amino: --NR.sup.1R.sup.2, wherein R.sup.1 and R.sup.2 are
independently amino substituents, for example, hydrogen, a
C.sub.1-7 alkyl group (also referred to as C.sub.1-7 alkylamino or
di-C.sub.1-7 alkylamino), a C.sub.3-20 heterocyclyl group, or a
C.sub.5-20aryl group, preferably H or a C.sub.1-7 alkyl group, or,
in the case of a "cyclic" amino group, R.sup.1 and R.sup.2, taken
together with the nitrogen atom to which they are attached, form a
heterocyclic ring having from 4 to 8 ring atoms. Amino groups may
be primary (--NH.sub.2), secondary (--NHR.sup.1), or tertiary
(--NHR.sup.1R.sup.2), and in cationic form, may be quaternary
(--.sup.+NR.sup.1R.sup.2R.sup.3). Examples of amino groups include,
but are not limited to, --NH.sub.2, --NHCH.sub.3,
--NHC(CH.sub.3).sub.2, --N(CH.sub.3).sub.2,
--N(CH.sub.2CH.sub.3).sub.2, and --NHPh. Examples of cyclic amino
groups include, but are not limited to, aziridino, azetidino,
pyrrolidino, piperidino, piperazino, morpholino, and
thiomorpholino.
[0081] Amidine (amidino): --C(.dbd.NR)NR.sub.2, wherein each R is
an amidine substituent, for example, hydrogen, a C.sub.1-7 alkyl
group, a C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably H or a C.sub.1-7 alkyl group. Examples of amidine groups
include, but are not limited to, --C(.dbd.NH)NH.sub.2,
--C(.dbd.NH)NMe.sub.2, and --C(.dbd.NMe)NMe.sub.2.
[0082] Nitro: --NO.sub.2.
[0083] Nitroso: --NO.
[0084] Cyano (nitrile, carbonitrile): --CN.
[0085] Sulfhydryl (thiol, mercapto): --SH.
[0086] Thioether (sulfide): --SR, wherein R is a thioether
substituent, for example, a C.sub.1-7 alkyl group (also referred to
as a C.sub.1-7 alkylthio group), a C.sub.3-20 heterocyclyl group,
or a C.sub.5-20 aryl group, preferably a C.sub.1-7 alkyl group.
Examples of C.sub.1-7 alkylthio groups include, but are not limited
to, --SCH.sub.3 and --SCH.sub.2CH.sub.3.
[0087] Disulfide: --SS--R, wherein R is a disulfide substituent,
for example, a C.sub.1-7 alkyl group, a C.sub.3-20 heterocyclyl
group, or a C.sub.5-20 aryl group, preferably a C.sub.1-7 alkyl
group (also referred to herein as C.sub.1-7 alkyl disulfide).
Examples of C.sub.1-7 alkyl disulfide groups include, but are not
limited to, --SSCH.sub.3 and --SSCH.sub.2CH.sub.3.
[0088] Sulfine (sulfinyl, sulfoxide): --S(.dbd.O)R, wherein R is a
sulfine substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably a C.sub.1-7 alkyl group. Examples of sulfine groups
include, but are not limited to, --S(.dbd.O)CH.sub.3 and
--S(.dbd.O)CH.sub.2CH.sub.3.
[0089] Sulfone (sulfonyl): --S(.dbd.O).sub.2R, wherein R is a
sulfone substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably a C.sub.1-7 alkyl group, including, for example, a
fluorinated or perfluorinated C.sub.1-7 alkyl group. Examples of
sulfone groups include, but are not limited to,
--S(.dbd.O).sub.2CH.sub.3 (methanesulfonyl, mesyl),
--S(.dbd.O).sub.2CF.sub.3 (triflyl),
--S(.dbd.O).sub.2CH.sub.2CH.sub.3 (esyl),
--S(.dbd.O).sub.2C.sub.4F.sub.9 (nonaflyl),
--S(.dbd.O).sub.2CH.sub.2CF.sub.3 (tresyl),
--S(.dbd.O).sub.2CH.sub.2CH.sub.2NH.sub.2 (tauryl),
--S(.dbd.O).sub.2Ph (phenylsulfonyl, besyl), 4-methylphenylsulfonyl
(tosyl), 4-chlorophenylsulfonyl (closyl), 4-bromophenylsulfonyl
(brosyl), 4-nitrophenyl (nosyl), 2-naphthalenesulfonate (napsyl),
and 5-dimethylamino-naphthalen-1-ylsulfonate (dansyl).
[0090] Sulfinic acid (sulfino): --S(.dbd.O)OH, --SO.sub.2H.
[0091] Sulfonic acid (sulfo): --S(.dbd.O).sub.2OH, --SO.sub.3H.
[0092] Sulfinate (sulfinic acid ester): --S(.dbd.O)OR; wherein R is
a sulfinate substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably a C.sub.1-7 alkyl group. Examples of sulfinate groups
include, but are not limited to, --S(.dbd.O)OCH.sub.3
(methoxysulfinyl; methyl sulfinate) and
--S(.dbd.O)OCH.sub.2CH.sub.3 (ethoxysulfinyl; ethyl sulfinate).
[0093] Sulfinyloxy: --OS(.dbd.O)R, wherein R is a sulfinyloxy
substituent, for example, a C.sub.1-7 alkyl group, a C.sub.3-20
heterocyclyl group, or a C.sub.5-20 aryl group, preferably a
C.sub.1-7 alkyl group. Examples of sulfinyloxy groups include, but
are not limited to, --OS(.dbd.O)CH.sub.3 and
--OS(.dbd.O)CH.sub.2CH.sub.3.
[0094] Sulfamyl (sulfamoyl; sulfinic acid amide; sulfinamide):
--S(.dbd.O)NR.sup.1R.sup.2, wherein R.sup.1 and R.sup.2 are
independently amino substituents, as defined for amino groups.
Examples of sulfamyl groups include, but are not limited to,
--S(.dbd.O)NH.sub.2, --S(.dbd.O)NH(CH.sub.3),
--S(.dbd.O)N(CH.sub.3).sub.2, --S(.dbd.O)NH(CH.sub.2CH.sub.3),
--S(.dbd.O)N(CH.sub.2CH.sub.3).sub.2, and --S(.dbd.O)NHPh.
[0095] Sulfonamido (sulfinamoyl; sulfonic acid amide; sulfonamide):
--S(.dbd.O).sub.2NR.sup.1R.sup.2, wherein R.sup.1 and R.sup.2 are
independently amino substituents, as defined for amino groups.
Examples of sulfonamido groups include, but are not limited to,
--S(.dbd.O).sub.2NH.sub.2, --S(.dbd.O).sub.2NH(CH.sub.3),
--S(.dbd.O).sub.2N(CH.sub.3).sub.2,
--S(.dbd.O).sub.2NH(CH.sub.2CH.sub.3),
--S(.dbd.O).sub.2N(CH.sub.2CH.sub.3).sub.2, and
--S(.dbd.O).sub.2NHPh.
[0096] Sulfonamino: --NR.sup.1S(.dbd.O).sub.2R, wherein R.sup.1 is
an amino substituent, as defined for amino groups, and R is a
sulfonamino substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably a C.sub.1-7 alkyl group. Examples of sulfonamino groups
include, but are not limited to, --NHS(.dbd.O).sub.2CH.sub.3 and
--N(CH.sub.3)S(.dbd.O).sub.2C.sub.6H.sub.5.
[0097] Sulfinamino: --NR.sup.1S(.dbd.O)R, wherein R.sup.1 is an
amino substituent, as defined for amino groups, and R is a
sulfinamino substituent, for example, a C.sub.1-7 alkyl group, a
C.sub.3-20 heterocyclyl group, or a C.sub.5-20 aryl group,
preferably a C.sub.1-7 alkyl group. Examples of sulfinamino groups
include, but are not limited to, --NHS(.dbd.O)CH.sub.3 and
--N(CH.sub.3)S(.dbd.O)C.sub.6H.sub.5.
[0098] As already mentioned, the above described groups may be
substituted, and particular examples include, but are not limited
to, C.sub.3-20 aryl-C.sub.1-7 alkyl groups, which include benzyl
(phenylmethyl, PhCH.sub.2--), benzhydryl (Ph.sub.2CH--), trityl
(triphenylmethyl, Ph.sub.3C--), phenethyl (phenylethyl,
Ph-CH.sub.2CH.sub.2--), styryl (Ph-CH.dbd.CH--) and cinnamyl
(Ph-CH.dbd.CH--CH.sub.2--).
Bidentate Groups
[0099] (i.e. groups with two points of covalent attachment; linking
groups) Alkylene: The term "C.sub.1-3 alkylene", as used herein,
pertains to a bidentate moiety obtained by removing two hydrogen
atoms from each of two different carbon atoms, of a linear
hydrocarbon compound having from 1 to 3 carbon atoms, which may be
saturated or unsaturated. Thus, the term "alkylene" includes the
sub-classes alkenylene and alkynylene.
[0100] In this context, the prefix C.sub.1-3 denotes the number of
carbon atoms, or range of number of carbon atoms.
[0101] Examples of saturated C.sub.1-3 alkylene groups include
--CH.sub.2-- (methylene), --CH.sub.2CH.sub.2-- (ethylene) and
--CH.sub.2CH.sub.2CH.sub.2-- (propylene).
[0102] Examples of unsaturated C.sub.1-3 alkylene groups (which may
be termed "C.sub.2-3 alkenylene" or "C.sub.2-3 alkynylene", as
appropriate) include --CH.dbd.CH-- (vinylene),
--CH.dbd.CH--CH.sub.2--, --CH.sub.2--CH.dbd.CH--, --C.ident.C--,
--C.ident.C--CH.sub.2-- and --CH.sub.2--C.ident.C--.
[0103] The C.sub.2-3 alkylene group may be substituted by any
monodentate substituent described above.
[0104] Alkoxylene: The term "alkoxylene," as used herein, pertains
to a bidentate group of formula --O(CH.sub.2).sub.nO--, where n is
1 or 2.
Includes Other Forms
[0105] Unless otherwise specified, included in the above are the
well known ionic, salt, solvate, and protected forms of these
substituents. For example, a reference to carboxylic acid (--COOH)
also includes the anionic (carboxylate) form (--COO.sup.-), a salt
or solvate thereof, as well as conventional protected forms.
Similarly, a reference to an amino group includes the protonated
form (--N.sup.+HR.sup.1R.sup.2), a salt or solvate of the amino
group, for example, a hydrochloride salt, as well as conventional
protected forms of an amino group. Similarly, a reference to a
hydroxyl group also includes the anionic form (--O.sup.-), a salt
or solvate thereof, as well as conventional protected forms of a
hydroxyl group.
Isomers, Salts, Solvates and Protected Forms
[0106] Certain compounds may exist in one or more particular
geometric, optical, enantiomeric, diasteriomeric, epimeric,
stereoisomeric, tautomeric, conformational, or anomeric forms,
including but not limited to, cis- and trans-forms; E- and Z-forms;
c-, t-, and r-forms; endo- and exo-forms; R-, S-, and meso-forms;
D- and L-forms; d- and l-forms; (+) and (-) forms; keto-, enol-,
and enolate-forms; syn- and anti-forms; synclinal- and
anticlinal-forms; .alpha.- and .beta.-forms; axial and equatorial
forms; boat-, chair-, twist-, envelope-, and halfchair-forms; and
combinations thereof, hereinafter collectively referred to as
"isomers" (or "isomeric forms").
[0107] Note that, except as discussed below for tautomeric forms,
specifically excluded from the term "isomers", as used herein, are
structural (or constitutional) isomers (i.e. isomers which differ
in the connections between atoms rather than merely by the position
of atoms in space). For example, a reference to a methoxy group,
--OCH.sub.3, is not to be construed as a reference to its
structural isomer, a hydroxymethyl group, --CH.sub.2OH. Similarly,
a reference to ortho-chlorophenyl is not to be construed as a
reference to its structural isomer, meta-chlorophenyl. However, a
reference to a class of structures may well include structurally
isomeric forms falling within that class (e.g. C.sub.1-7alkyl
includes n-propyl and iso-propyl; butyl includes n-, iso-, sec-,
and tert-butyl; methoxyphenyl includes ortho-, meta-, and
para-methoxyphenyl).
[0108] The above exclusion does not pertain to tautomeric forms,
for example, keto-, enol-, and enolate-forms, as in, for example,
the following tautomeric pairs: keto/enol (illustrated below),
imine/enamine, amide/imino alcohol, amidine/amidine, nitroso/oxime,
thioketone/enethiol, N-nitroso/hyroxyazo, and nitro/aci-nitro.
##STR00008##
[0109] Note that specifically included in the term "isomer" are
compounds with one or more isotopic substitutions. For example, H
may be in any isotopic form, including .sup.1H, .sup.2H (D), and
.sup.3H (T); C may be in any isotopic form, including .sup.12C,
.sup.13C, and .sup.14C; O may be in any isotopic form, including
.sup.16O and .sup.18O; and the like.
[0110] Unless otherwise specified, a reference to a particular
compound includes all such isomeric forms, including (wholly or
partially) racemic and other mixtures thereof. Methods for the
preparation (e.g. asymmetric synthesis) and separation (e.g.
fractional crystallisation and chromatographic means) of such
isomeric forms are either known in the art or are readily obtained
by adapting the methods taught herein, or known methods, in a known
manner.
[0111] Unless otherwise specified, a reference to a particular
compound also includes ionic, salt, solvate, and protected forms of
thereof, for example, as discussed below.
[0112] It may be convenient or desirable to prepare, purify, and/or
handle a corresponding salt of the active compound, for example, a
pharmaceutically-acceptable salt. Examples of pharmaceutically
acceptable salts are discussed in Berge, et al., J. Pharm. Sci.,
66, 1-19 (1977).
[0113] For example, if the compound is anionic, or has a functional
group which may be anionic (e.g. --COOH may be --COO.sup.-), then a
salt may be formed with a suitable cation. Examples of suitable
inorganic cations include, but are not limited to, alkali metal
ions such as Na.sup.+ and K.sup.+, alkaline earth cations such as
Ca.sup.2+ and Mg.sup.2+, and other cations such as Al.sup.+3.
Examples of suitable organic cations include, but are not limited
to, ammonium ion (i.e. NH.sub.4.sup.+) and substituted ammonium
ions (e.g. NH.sub.3R.sup.+, NH.sub.2R.sub.2.sup.+, NHR.sub.3.sup.+,
NR.sub.4.sup.+). Examples of some suitable substituted ammonium
ions are those derived from: ethylamine, diethylamine,
dicyclohexylamine, triethylamine, butylamine, ethylenediamine,
ethanolamine, diethanolamine, piperazine, benzylamine,
phenylbenzylamine, choline, meglumine, and tromethamine, as well as
amino acids, such as lysine and arginine. An example of a common
quaternary ammonium ion is N(CH.sub.3).sub.4.sup.+.
[0114] If the compound is cationic, or has a functional group which
may be cationic (e.g. --NH.sub.3 may be --NH.sub.3.sup.+), then a
salt may be formed with a suitable anion. Examples of suitable
inorganic anions include, but are not limited to, those derived
from the following inorganic acids: hydrochloric, hydrobromic,
hydroiodic, sulfuric, sulfurous, nitric, nitrous, phosphoric, and
phosphorous.
[0115] Examples of suitable organic anions include, but are not
limited to, those derived from the following organic acids:
2-acetyoxybenzoic, acetic, ascorbic, aspartic, benzoic,
camphorsulfonic, cinnamic, citric, edetic, ethanedisulfonic,
etharasulfonic, fumaric, glucoheptonic, gluconic, glutamic,
glycolic, hydroxymaleic, hydroxynaphthalene carboxylic, isethionic,
lactic, lactobionic, lauric, maleic, malic, methanesulfonic, mucic,
oleic, oxalic, palmitic, pamoic, pantothenic, phenylacetic,
phenylsulfonic, propionic, pyruvic, salicylic, stearic, succinic,
sulfanilic, tartaric, toluenesulfonic, and valeric. Examples of
suitable polymeric organic anions include, but are not limited to,
those derived from the following polymeric acids: tannic acid,
carboxymethyl cellulose.
[0116] It may be convenient or desirable to prepare, purify, and/or
handle a corresponding solvate of the active compound. The term
"solvate" is used herein in the conventional sense to refer to a
complex of solute (e.g., active compound, salt of active compound)
and solvent. If the solvent is water, the solvate may be
conveniently referred to as a hydrate, for example, a mono-hydrate,
a di-hydrate, a tri-hydrate, etc.
[0117] It may be convenient or desirable to prepare, purify, and/or
handle the active compound in a chemically protected form. The term
"chemically protected form" is used herein in the conventional
chemical sense and pertains to a compound in which one or more
reactive functional groups are protected from undesirable chemical
reactions under specified conditions (e.g. pH, temperature,
radiation, solvent, and the like). In practice, well known chemical
methods are employed to reversibly render unreactive a functional
group, which otherwise would be reactive, under specified
conditions. In a chemically protected form, one or more reactive
functional groups are in the form of a protected or protecting
group (also known as a masked or masking group or a blocked or
blocking group). By protecting a reactive functional group,
reactions involving other unprotected reactive functional groups
can be performed, without affecting the protected group; the
protecting group may be removed, usually in a subsequent step,
without substantially affecting the remainder of the molecule. See,
for example, Protective Groups in Organic Synthesis (T. Green and
P. Wuts; 3rd Edition; John Wiley and Sons, 1999).
[0118] A wide variety of such "protecting", "blocking", or
"masking" methods are widely used and well known in organic
synthesis. For example, a compound which has two nonequivalent
reactive functional groups, both of which would be reactive under
specified conditions, may be derivatized to render one of the
functional groups "protected," and therefore unreactive, under the
specified conditions; so protected, the compound may be used as a
reactant which has effectively only one reactive functional group.
After the desired reaction (involving the other functional group)
is complete, the protected group may be "deprotected" to return it
to its original functionality.
[0119] For example, a hydroxy group may be protected as an ether
(--OR) or an ester (--OC(.dbd.O)R), for example, as: a t-butyl
ether; a benzyl, benzhydryl (diphenylmethyl), or trityl
(triphenylmethyl)ether; a trimethylsilyl or t-butyldimethylsilyl
ether; or an acetyl ester (--OC(.dbd.O)CH.sub.3, --OAc).
[0120] For example, an aldehyde or ketone group may be protected as
an acetal (R--CH(OR).sub.2) or ketal (R.sub.2C(OR).sub.2),
respectively, in which the carbonyl group (>C.dbd.O) is
converted to a diether (>C(OR).sub.2), by reaction with, for
example, a primary alcohol. The aldehyde or ketone group is readily
regenerated by hydrolysis using a large excess of water in the
presence of acid.
[0121] For example, an amine group may be protected, for example,
as an amide (--NRCO--R) or a urethane (--NRCO--OR), for example,
as: an acetamide (--NHCO--CH.sub.3); a benzyloxy amide
(--NHCO--OCH.sub.2C.sub.6H.sub.5, --NH-Cbz); as a t-butoxy amide
(--NHCO--OC(CH.sub.3).sub.3, --NH-Boc); a 2-biphenyl-2-propoxy
amide (--NHCO--OC(CH.sub.3).sub.2C.sub.6H.sub.4C.sub.6H.sub.5,
--NH-Bpoc), as a 9-fluorenylmethoxy amide (--NH-Fmoc), as a
6-nitroveratryloxy amide (--NH-Nvoc), as a 2-trimethylsilylethyloxy
amide (--NH-Teoc), as a 2,2,2-trichloroethyloxy amide (--NH-Troc),
as an allyloxy amide (--NH-Alloc), as a 2(-phenylsulfonyl)ethyloxy
amide (--NH-Psec); or, in suitable cases (e.g., cyclic amines), as
a nitroxide radical (>N--O).
[0122] For example, a carboxylic acid group may be protected as an
ester for example, as: an C.sub.1-7 alkyl ester (e.g., a methyl
ester; a t-butyl ester); a C.sub.1-7 haloalkyl ester (e.g., a
C.sub.1-7 trihaloalkyl ester); a triC.sub.1-7 alkylsilyl-C.sub.1-7
alkyl ester; or a C.sub.5-20 aryl-C.sub.1-7 alkyl ester (e.g. a
benzyl ester; a nitrobenzyl ester); or as an amide, for example, as
a methyl amide.
[0123] For example, a thiol group may be protected as a thioether
(--SR), for example, as: a benzyl thioether; an acetamidomethyl
ether (--S--CH.sub.2NHC(.dbd.O)CH.sub.3).
[0124] The term "treatment", as used herein in the context of
treating a condition, pertains generally to treatment and therapy,
whether of a human or an animal (e.g. in veterinary applications),
in which some desired therapeutic effect is achieved, for example,
the inhibition of the progress of the condition, and includes a
reduction in the rate of progress, a halt in the rate of progress,
amelioration of the condition, and cure of the condition. Treatment
as a prophylactic measure (i.e. prophylaxis) is also included.
[0125] The term "therapeutically-effective amount", as used herein,
pertains to that amount of an active compound, or a material,
composition or dosage form comprising an active compound, which is
effective for producing some desired therapeutic effect,
commensurate with a reasonable benefit/risk ratio, when
administered in accordance with a desired treatment regimen.
Suitable dose ranges will typically be in the range of from 0.01 to
20 mg/kg/day, preferably from 0.1 to 10 mg/kg/day.
Compositions and their Administration
[0126] Compositions may be formulated for any suitable route and
means of administration. Pharmaceutically acceptable carriers or
diluents include those used in formulations suitable for oral,
rectal, nasal, topical (including buccal and sublingual), vaginal
or parenteral (including subcutaneous, intramuscular, intravenous,
intradermal, intrathecal and epidural) administration. The
formulations may conveniently be presented in unit dosage form and
may be prepared by any of the methods well known in the art of
pharmacy. Such methods include the step of bringing into
association the active ingredient with the carrier which
constitutes one or more accessory ingredients. In general the
formulations are prepared by uniformly and intimately bringing into
association the active ingredient with liquid carriers or finely
divided solid carriers or both, and then, if necessary, shaping the
product.
[0127] For solid compositions, conventional non-toxic solid
carriers include, for example, pharmaceutical grades of mannitol,
lactose, cellulose, cellulose derivatives, starch, magnesium
stearate, sodium saccharin, talcum, glucose, sucrose, magnesium
carbonate, and the like may be used. The active compound as defined
above may be formulated as suppositories using, for example,
polyalkylene glycols, acetylated triglycerides and the like, as the
carrier. Liquid pharmaceutically administrable compositions can,
for example, be prepared by dissolving, dispersing, etc, an active
compound as defined above and optional pharmaceutical adjuvants in
a carrier, such as, for example, water, saline aqueous dextrose,
glycerol, ethanol, and the like, to thereby form a solution or
suspension. If desired, the pharmaceutical composition to be
administered may also contain minor amounts of non-toxic auxiliary
substances such as wetting or emulsifying agents, pH buffering
agents and the like, for example, sodium acetate, sorbitan
monolaurate, triethanolamine sodium acetate, sorbitan monolaurate,
triethanolamine oleate, etc. Actual methods of preparing such
dosage forms are known, or will be apparent, to those skilled in
this art; for example, see Remington's Pharmaceutical Sciences,
20th edition, pub. Lippincott, Williams & Wilkins, 2000. The
composition or formulation to be administered will, in any event,
contain a quantity of the active compound(s) in an amount effective
to alleviate the symptoms of the subject being treated.
[0128] Dosage forms or compositions containing active ingredient in
the range of 0.25 to 95% with the balance made up from non-toxic
carrier may be prepared.
[0129] For oral administration, a pharmaceutically acceptable
non-toxic composition is formed by the incorporation of any of the
normally employed excipients, such as, for example, pharmaceutical
grades of mannitol, lactose, cellulose, cellulose derivatives,
sodium crosscarmellose, starch, magnesium stearate, sodium
saccharin, talcum, glucose, sucrose, magnesium carbonate, and the
like. Such compositions take the form of solutions, suspensions,
tablets, pills, capsules, powders, sustained release formulations
and the like. Such compositions may contain 1%-95% active
ingredient, more preferably 2-50%, most preferably 5-8%.
[0130] Parenteral administration is generally characterized by
injection, either subcutaneously, intramuscularly or intravenously.
Injectables can be prepared in conventional forms, either as liquid
solutions or suspensions, solid forms suitable for solution or
suspension in liquid prior to injection, or as emulsions. Suitable
excipients are, for example, water, saline, dextrose, glycerol,
ethanol or the like. In addition, if desired, the pharmaceutical
compositions to be administered may also contain minor amounts of
non-toxic auxiliary substances such as wetting or emulsifying
agents, pH buffering agents and the like, such as for example,
sodium acetate, sorbitan monolaurate, triethanolamine oleate,
triethanolamine sodium acetate, etc.
[0131] The percentage of active compound contained in such parental
compositions is highly dependent on the specific nature thereof, as
well as the activity of the compound and the needs of the subject.
However, percentages of active ingredient of 0.1% to 10% in
solution are employable, and will be higher if the composition is a
solid which will be subsequently diluted to the above percentages.
Preferably, the composition will comprise 0.2-2% of the active
agent in solution.
[0132] Ointments are typically prepared from the active compound
and a paraffinic or a water-miscible ointment base.
[0133] Creams are typically prepared from the active compound and
an oil-in-water cream base. If desired, the aqueous phase of the
cream base may include, for example, at least about 30% w/w of a
polyhydric alcohol, i.e., an alcohol having two or more hydroxyl
groups such as propylene glycol, butane-1,3-diol, mannitol,
sorbitol, glycerol and polyethylene glycol and mixtures thereof.
The topical formulations may desirably include a compound which
enhances absorption or penetration of the active compound through
the skin or other affected areas. Examples of such dermal
penetration enhancers include dimethylsulfoxide and related
analogues.
[0134] Formulations suitable for vaginal administration may be
presented as pessaries, tampons, creams, gels, pastes, foams or
spray formulations containing in addition to the active compound,
such carriers as are known in the art to be appropriate.
Acronyms
[0135] For convenience, many chemical moieties are represented
using well known abbreviations, including but not limited to,
methyl (Me), ethyl (Et), n-propyl (nPr), iso-propyl (iPr), n-butyl
(nBu), sec-butyl (sBu), iso-butyl (iBu), tert-butyl (tBu), n-hexyl
(nHex), cyclohexyl (cHex), phenyl (Ph), biphenyl (biPh), benzyl
(Bn), naphthyl (naph), methoxy (MeO), ethoxy (EtO), benzoyl (Bz),
and acetyl (Ac).
[0136] For convenience, many chemical compounds are represented
using well known abbreviations, including but not limited to,
methanol (MeOH), ethanol (EtOH), iso-propanol (i-PrOH), methyl
ethyl ketone (MEK), ether or diethyl ether (Et.sub.2O), acetic acid
(AcOH), dichloromethane (methylene chloride, DCM), acetonitrile
(ACN), trifluoroacetic acid (TFA), dimethylformamide (DMF),
tetrahydrofuran (THF), and dimethylsulfoxide (DMSO).
General Synthesis Methods
[0137] Compounds where R.sup.2 is tetrazol-5-yl may be synthesised
from compounds of formula 4:
##STR00009##
wherein B' represents the aromatic moiety in B, R' represents the
C.sub.m alkylene group in B, and R' is on the appropriate position
on the aromatic moiety, by treatment with sodium azide,
trimethyltin azide or trimethylsilyl azide.
[0138] Compounds of formula 4, where D is
--C(.dbd.O)--N(R.sup.N)--, may be synthesised by coupling compounds
of Formula 5 and Formula 6a, wherein the groups B' and R' are as
defined above.
##STR00010##
[0139] Such a coupling step may be carried out using a coupling
agent or agents, for example,
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate, TBTU and DIPEA, or EDC and HOAt.
[0140] Compounds of formula 4, where D is
--N(R.sup.N)--C(.dbd.O)--, may be synthesised by coupling compounds
of Formula 5' and Formula 6a', wherein the groups B' and R' are as
defined above.
##STR00011##
[0141] Such a coupling step may be carried out using a coupling
agent or agents, as described above.
[0142] Compounds where R.sup.2 is carboxy, may be synthesised from
compounds of formula 7:
##STR00012##
wherein B' and R' are as defined above, by a hydrolysis reaction,
for example, using sodium hydroxide.
[0143] Compounds of formula 7, where D is
--C(.dbd.O)--N(R.sup.N)--, can be synthesised by coupling compounds
of formula 5 and 6b, wherein B' and R' are as defined above:
##STR00013##
[0144] Such a coupling step may be carried out as described above,
by using a coupling agent or agents, for example,
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate, TBTU and DIPEA, or EDC and HOAt.
[0145] Compounds of formula 7, where D is
--N(R.sup.N)--C(.dbd.O)--, may be synthesised by coupling compounds
of Formula 5' and Formula 6b', wherein the groups B' and R' are as
defined above.
##STR00014##
[0146] Such a coupling step may be carried out using a coupling
agent or agents, as described above.
[0147] Compounds of formula 5, where R.sup.5 is an aryl group, may
be synthesised from compounds of formula 8:
##STR00015##
by a Suzuki coupling of a compound of formula 9a (or equivalent
ester of formula 9b):
##STR00016##
[0148] The Suzuki coupling may be achieved using, for example,
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (II) as the
palladium catalyst. Alternatively, the coupling may be achieved
using CsCO.sub.3, with Pd(PPh.sub.3).sub.4 as the palladium
catalyst. In this reaction, the carboxy group may be protected.
[0149] Compounds of Formula 8, where A is:
##STR00017##
may be synthesised from compounds of formula 10:
##STR00018##
by treating the compound of formula 10 with a brominating agent,
such as pyridinium tribromide. This method can be readily adapted
for other A groups.
[0150] Compounds of formula 7 where R.sup.5 is an optionally
substituted C.sub.5-7 aryl group may be prepared from compounds of
formula 7 where R.sup.5 is bromine by a Suzuki coupling with
compounds of formula 9a or 9b.
[0151] Compounds of formula 5, where R.sup.5 is an alkyl group, and
where A is:
##STR00019##
may be synthesized from compounds of formula 11:
##STR00020##
by reaction with R.sup.5--Br, in the presence of AlCl.sub.2, in an
organic solvent, such as ortho-dichlorobenzene, followed by
deprotection of the acid group. This method can be readily adapted
for other A groups.
[0152] Compounds of formula 7, where D is --CH.sub.2--O-- or
--CH.sub.2--S--, may be prepared by coupling compounds of formula
5'' and 6b'', wherein B' and R' are as defined above:
##STR00021##
where X'' is O or S, using NaH in an organic solvent, such as DMF
and heptane or THF. Alternatively the coupling may take place
before the addition of the R'CO.sub.2R.sup.O group.
[0153] A key step in the synthesis of compounds of formula 7, where
D is --C(.dbd.O)--CH.sub.2--, is the coupling of the remainder of
the molecule to R.sup.5-A. This can be achieved by coupling a
compound of formula 12:
##STR00022##
or precursor thereof to R.sup.5-A by a suitable method. For
example, when A is:
##STR00023##
the coupling may take place in an organic solvent in the presence
of P.sub.2O.sub.5.
Preferences
[0154] The following preferences may be combined with one another,
and may be different for each aspect of the present invention.
[0155] R.sup.5 may be a C.sub.5-7 aryl group, such as furan-2-yl
and phenyl.
[0156] R.sup.5 is preferably a C.sub.6 aryl group, and is more
preferably phenyl. R.sup.5 may be substituted, and preferred
substituents include C.sub.1-7 alkoxy groups, more preferably
C.sub.1-4 alkoxy groups, e.g. --OMe, --OCF.sub.3, --OEt,
--OCHF.sub.2, with --OCHF.sub.2 being the most preferred.
[0157] When R.sup.5 is phenyl, preferable substituents include:
C.sub.1-4 alkyl (e.g. methyl, --CF.sub.3, isopropyl); C.sub.1-4
alkoxy (e.g. methoxy, --OCF.sub.3), including substituted C.sub.1-4
alkoxy (e.g. benzyloxy); C.sub.5-6 aryl (e.g. phenyl); halo (e.g.
Cl, F, di-Cl); acyl (e.g. --COMe); amino (e.g. --NH.sub.2,
--NMe.sub.2); alkoxylene (e.g. --O--CH.sub.2--O--). In some
embodiments, C.sub.1-4 alkyl (e.g. methyl, --CF.sub.3, isopropyl);
C.sub.1-4 alkoxy (e.g. methoxy, --OCF.sub.3); halo (e.g. Cl, F,
di-Cl); acyl (e.g. --COMe); and alkoxylene (e.g.
--O--CH.sub.2--O--) are preferred.
[0158] The substituents may be any position of the phenyl ring,
e.g. 2-, 3- and 4-, and when there are two substituents (e.g.
di-chloro), these may be, for example, at: 2-,3-; 2-,4-; 3-,5- or
3-,4-.
[0159] R.sup.5 may preferably be furan-2-yl.
[0160] R.sup.5 may preferably be a C.sub.9-10 aryl group, e.g.
napthyl (more preferably napth-1-yl) and indolyl (more preferably
indol-4-yl).
[0161] When R.sup.5 is a C.sub.4-20 alkyl group, it may be a
C.sub.4-10 alkyl group, and preferably a branched C.sub.4-10 alkyl
group, e.g. t-butyl, --CH.sub.2--CH(CH.sub.3).sub.2 or a cyclic
alkyl group, such as cyclohexyl or adamantyl. Of these the cyclic
groups are more preferred, with adamantyl being the most
preferred.
[0162] When A is a five membered ring:
(i) R.sup.3 (if present) is preferably selected from H and
optionally substituted C.sub.1-4 alkyl (in particular, methyl) and
is most preferably H; and (ii) R.sup.4 is preferably selected from
H and optionally substituted C.sub.1-4 alkyl (in particular,
methyl) and is most preferably H.
[0163] When A is a six-membered ring, it is preferred that
either:
(i) R.sup.3, R.sup.4 and R.sup.6 (if present) are H; or (ii) one of
R.sup.3, R.sup.4 and R.sup.6 (if present) are Cl or F.
[0164] One preferred option when A is:
##STR00024##
is for R.sup.4 to be F.
[0165] A is preferably selected from:
##STR00025##
and is more preferably selected from:
##STR00026##
[0166] A is most preferably selected from:
##STR00027##
[0167] The most preferred option for A is:
##STR00028##
[0168] D is preferably selected from:
##STR00029##
and is more preferably:
##STR00030##
[0169] R.sup.N is preferably H or methyl, and is more preferably
H.
[0170] B is preferably:
##STR00031##
and more preferably:
##STR00032##
[0171] R.sup.2 is preferably carboxy or tetrazoly-5-yl, with
carboxy being most preferred.
[0172] When R.sup.P4 is H, R.sup.P3 is preferably
--CH.dbd.CH--R.sup.2.
[0173] In some embodiments, m and n can only be 0 or 1, and m+n can
only be 1 or 2. In these embodiments, preferably n+m=1, and more
preferably n is 0 and m is 1.
[0174] In other embodiments, it is preferred that n is 0, and one
of R.sup.P3 and R.sup.P4 (preferably R.sup.P3) is
--O--CH.sub.2--R.sup.2, wherein R.sup.2 is preferably carboxy or
tetrazol-5-yl, more preferably carboxy.
[0175] In some embodiments, the compound is of formula (Ia):
##STR00033##
or of formula (Ib):
##STR00034##
[0176] Particularly preferred compounds of the present invention
include: [0177]
{4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic acid (2);
[0178] 4-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic acid
(4); [0179] 4-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic
acid (10); [0180]
(3-[(5-(4-Methoxy-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic
acid (12); [0181]
(3-[(5-(4-Dimethylamino-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic
acid (14); and [0182]
3-{4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic acid
(16).
[0183] Further particularly preferred compounds of the invention
include: [0184]
(3-{[5-(2-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (17); [0185]
(3-{[5-(3-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (18); [0186]
(3-{[5-(3-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (19); [0187]
(3-{[5-(4-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (20); [0188]
(3-{[5-(3-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (21); [0189]
(3-{[5-(4-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (22); [0190]
(3-{[5-(2-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (23); [0191]
(3-{[5-(3-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (24); [0192]
(3-{[5-(2,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (25); [0193]
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (26); [0194]
(3-{[5-(3,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (27); [0195]
(3-{[5-(2-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (28); [0196]
(3-{[5-(4-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (29); [0197]
(3-{[5-(2-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (30); [0198]
(3-{[5-Naphthalen-1-yl-furan-2-carbonyl)-amino]-phenyl}-acetic acid
(31); [0199]
(3-{[5-(3-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl-
)-acetic acid (32); [0200]
(3-{[5-(4-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-aceti-
c acid (33); [0201]
(3-{[5-(3-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (34); [0202]
(3-{[5-(4-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (35); [0203]
{3-[(5-Benzo[1,3]dioxol-5-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid (36); [0204]
(3-{[5-(2,3-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (37); [0205]
{3-[([2,2']Bifuranyl-5-carbonyl)-amino]-phenyl}-acetic acid (38);
[0206]
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (39); [0207]
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (40); [0208]
3-{[5-(1H-Indol-5-yl)-furan-2-carbonyl]-amino}-phenyl)-acetic acid
(41); [0209]
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (42); [0210]
{3-[(5-Phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic acid
(43); [0211]
{3-[(4-Chloro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid (44);
[0212] {3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acetic
acid (45); [0213]
{3-[(6-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid (46);
[0214] {3-[(3-Methyl-biphenyl-4-carbonyl)-amino]-phenyl}-acetic
acid (47); [0215]
{3-[(3-Chloro-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid (48)
[0216] {3-[(Biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid (49);
[0217]
{3-[(4-Methyl-5-phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic
acid (50); [0218]
{3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid (51);
[0219] ({3-[(5-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic
acid (52); [0220]
{3-[(2-Phenyl-1H-imidazole-5-carbonyl)-amino]-phenyl}-acetic acid
(53); [0221]
{3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acetic acid (54);
[0222] 3-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic acid
(57); [0223]
5-[(5-Phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic acid
(59); [0224]
3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acrylic acid (61);
[0225] 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic
acid (62); [0226]
6-[(5-Phenyl-furan-2-carbonyl)-amino]-naphthalene-2-carboxylic acid
(63); [0227]
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (66); [0228]
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (68); [0229]
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (69); [0230]
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (70); [0231]
3-(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (71); [0232]
5-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-1H-indole-2-carboxylic
acid (72); [0233] 5-Phenyl-furan-2-carboxylic acid
(3-carbamoylmethyl-phenyl)-amide (73); [0234]
Phenyl-furan-2-carboxylic acid [3-(2-hydroxy-ethyl)-phenyl]-amide
(74); and [0235] 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (75).
[0236] Further particularly preferred compounds of the invention
include: 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-yl)-phenyl]-amide (177); [0237]
5-(3-Chloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (81); [0238]
5-(3,5-Dichloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (82); [0239]
5-(4-Fluoro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (85); [0240]
5-(3-Fluoro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (86); [0241]
5-(4-Chloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (87); [0242]
5-Phenyl-furan-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]-phenyl}-amide (89); [0243]
5-(3-Chloro-phenyl)-furan-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]-phenyl}-amide (90); [0244]
6-Phenyl-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (92); [0245]
6-(4-Fluoro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (93); [0246]
6-(3-Fluoro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (94); [0247]
6-(4-Chloro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (95); [0248]
5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzofuran-2-carboxylic acid
(96); [0249]
5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzo[b]thiophene-2-carboxyl-
ic acid (97); [0250]
2-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-benzylidene}-butyric acid
(98); [0251]
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acryli-
c acid (100); [0252]
3-{3-[(5-Benzo[1,3]dioxol-5-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (101); [0253]
3-(3-{[5-(3,5-Bis-trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}phenyl)-
-acrylic acid (102); [0254]
3-{3-[(5-Biphenyl-3-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (103); [0255]
3-(3-{[5-(3-Benzyloxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (104); [0256]
3-(3-{[5-(2-Fluoro-biphenyl-4-yl)-furan-2-carbonyl]-amino}-phenyl)-acryli-
c acid (105); [0257]
3-{3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic acid
(107); [0258]
3-{3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (108); [0259]
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (110); [0260]
3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(111); [0261]
3-{3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (112); [0262]
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (113); [0263]
3-{3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acrylic acid
(115); [0264]
3-(3-{[2-(3-Fluoro-phenyl)-thiazole-4-carbonyl]-amino}-phenyl)-acrylic
acid (116); [0265] [3-(Biphenyl-3-ylcarbamoyl)-phenyl]-acetic acid
(117); [0266]
1-Methyl-5-[(5-phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxy-
lic acid (118); [0267]
3-{3-[2--Oxo-2-(5-phenyl-furan-2-yl)-ethyl]-phenyl}-acrylic acid
(120); [0268] 3-[3-(2-Phenyl-thiazol-4-ylmethoxy)-phenyl]-acrylic
acid (121); [0269]
3-[3-(2-Phenyl-thiazol-4-ylmethylsulfanyl)-phenyl]-acrylic acid
(122); [0270]
3-{3-[(5-Adamantan-1-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (123); [0271]
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (125); [0272]
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (126); [0273]
(3-{[5-(3,5-Difluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (127); [0274]
(3-{[5-(3-fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (128); [0275]
(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (129); [0276]
(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (130); [0277]
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryli-
c acid (132); [0278]
(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (133); [0279]
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-propio-
nic acid (134); [0280]
5-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-1H-indole-2-carbo-
xylic acid (135); [0281]
3-(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (137); [0282]
(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (138); [0283]
{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (140); [0284]
3-{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (142); [0285]
{3-[(3',5'-Dichloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (143); [0286]
3-{3-[(3',5'-Dichloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acryli-
c acid (144); [0287]
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (146); [0288]
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (147); [0289]
3-(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (148); [0290]
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (150); [0291]
3-(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (151); [0292]
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (153); [0293]
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (154); [0294]
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (155); [0295]
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (156); [0296]
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (157); [0297]
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (158); [0298]
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]amino}-phenyl)-propionic
acid (159); [0299]
{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenoxy}-acetic acid (160);
[0300]
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-propionic
acid (162); [0301]
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (163); [0302]
3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic acid
(164); [0303]
3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid
(165); [0304]
3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic acid
(167); [0305]
(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (168); [0306]
{3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid
(169); [0307]
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (170); [0308]
{3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid
(171); [0309] 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide (173); [0310]
6-Phenyl-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide (174); [0311]
6-Phenyl-pyridine-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide (175); and [0312]
4-Fluoro-biphenyl-3-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide (176).
[0313] The selectivity of the compound for modulating EP.sub.2
receptors over one or more of the other EP receptors (i.e.
EP.sub.2, EP.sub.2, EP.sub.4) can be quantified by dividing the Ki
for EP.sub.2 (see below) by the Ki for the other EP receptors (see
below). The resulting ratio is preferably 10 or more, more
preferably 100 or more.
SYNTHESIS EXAMPLES
General Experimental Details
[0314] Petroleum ether refers to that fraction with a boiling point
of 40-60.degree. C.
[0315] Organic solutions were dried over magnesium sulphate unless
otherwise specified.
General Experimental Details for Examples 1 to 5
[0316] All reactions were carried out under an inert atmosphere of
nitrogen.
[0317] PS-TsCl refers to Polystyrene scavenger resin (loading 1.97
mmol/g)-Argonaut Technologies (P/N 800277)
LC/MS Systems
[0318] The Liquid Chromatography Mass Spectroscopy (LC/MS) systems
used are as follows.
LC/MS System A:
[0319] Mass Spectrometer--Platform LC with electrospray source
operating in positive and negative ion mode. HP1100 system running
at 2.0 mL/min, 200 .mu.L/min split to the ESI source with inline
HP1100 DAD detection and SEDEX ELS detection. [0320] Mobile Phase
[0321] A) Water 0.1% Formic Acid [0322] B) acetonitrile 0.1% Formic
Acid [0323] Gradient
TABLE-US-00001 [0323] Time Flow (min) (mL/min) % A % B 0.00 2.0 95
5 0.50 2.0 95 5 4.50 2.0 5 95 5.00 2.0 5 95 5.50 2.0 95 5
[0324] Column Luna 3u C18(2) 30.times.4.6 mm
LC/MS System B:
[0324] [0325] Mass Spectrometer--Platform II with electrospray
source operating in negative ion mode. HP1100 system running at 2.0
mL/min, 200 .mu.L/min split to the ESI source with inline HP1100
DAD detection and SEDEX ELS detection. [0326] Mobile Phase [0327]
A) Water 0.1 Diethylamine [0328] B) acetonitrile [0329]
Gradient
TABLE-US-00002 [0329] Time Flow (min) (mL/min) % A % B 0.00 2.0 95
5 0.50 2.0 95 5 4.00 2.0 5 95 4.50 2.0 5 95 5.00 2.0 95 5 20.00 2.0
95 5
[0330] Column--XTerra MS C18 3.5 .mu.m 4.6.times.30 mm
LCMS System C:
[0330] [0331] Mass Spectrometer--Finnigan TSQ700 with electrospray
source operating in negative ion mode. [0332] HP1050 system running
at 2.0 mL/min, 200 .mu.L/min split to the ESI source with inline
HP1050 Single wavelength UV detector at 254 nm. [0333] Mobile Phase
[0334] A) Water 0.1% Diethylamine [0335] B) acetonitrile [0336]
Gradient
TABLE-US-00003 [0336] Time Flow (min) (mL/min) % A % B 0.00 2.0 95
5 1.00 2.0 95 5 15.00 2.0 5 95 17.00 2.0 5 95 18.00 2.0 95 5 20.00
2.0 95 5
[0337] Column --XTerra MS C18 3.5 .mu.m 4.6.times.30 mm
LC/MS System D:
[0337] [0338] Mass Spectrometer--Finnigan TSQ700 with electrospray
source operating in positive or negative ion mode. HP1050 system
running at 2.0 mL/min, 200 .mu.L/min split to the ESI source with
inline HP1050 Single Wavelength UV detector at 254 nm. [0339]
Mobile Phase [0340] A) Water 0.1% formic Acid [0341] B)
acetonitrile 0.1% formic Acid [0342] Gradient
TABLE-US-00004 [0342] Time Flow (min) (mL/min) % A % B 0.00 2.0 95
5 1.00 2.0 95 5 15.00 2.0 5 95 17.00 2.0 5 95 18.00 2.0 95 5 20.00
2.0 95 5
[0343] Column Higgins Clipius C18 5 .mu.m 100.times.3.0 mm
Example 1
Synthesis of {4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid (2)
##STR00035##
[0344] (a) {4-[(5-phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid ethyl ester (1)
[0345] Diispropylethylamine (300 .mu.l) was added to a stirred
solution of 5-phenyl-furan-2-carboxylic acid (73.5 mg, 0.39 mmol)
and ethyl-4-aminophenyl acetate (70 mg, 0.39 mmoles) in
N,N-dimethylformamide (10 ml).
O-(7-Azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (200 mg, 0.52 mmoles) was added and the
solution was stirred at room temperature for 72 hours. The solvent
was evaporated, the residue was dissolved in dichloromethane and
washed with water, 10% aqueous sodium carbonate, 1 M aqueous
hydrochloric acid and finally dried (MgSO.sub.4). After evaporation
of the solvent, the residue was triturated with cyclohexane and
dried to afford (1) (82 mg) as a gum. LC/MS System A; R.sub.t=3.80
mins, m/z (ES.sup.+)=350 (M+H for C.sub.21H.sub.19NO.sub.4).
(b) {4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic acid
(2)
[0346] A solution of sodium hydroxide (100 mg) in water (5 ml) was
added to a stirred solution of
{4-[(5-phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic acid ethyl
ester (1) (75 mg, 0.214 mmoles) in ethanol (10 ml) and the mixture
was stirred at room temperature for 1 hour. The solvent was
evaporated and the residue was diluted with water (10 ml) and
acidified to pH=2 with 1 M aqueous hydrochloric acid. The
precipitate was collected, washed with water and the residue was
triturated with cyclohexane to afford (2) (61.5 mg) as a white
solid. LC/MS System D; R.sub.t=3.01 mins, m/z (ES-)=320 (M-H for
C.sub.19H.sub.15NO.sub.4.
Example 2
Synthesis of 4-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic
acid (4)
##STR00036##
[0347] (a) 4-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic
acid ethyl ester (3)
[0348] In an analogous manner to Example 1(a), compound (3) was
synthesised from 5-phenyl-furan-2-carboxylic acid (73.5 mg, 0.39
mmol) and 4-aminomethyl-benzoic acid ethyl ester (70 mg, 0.39
mmoles). 80 mg of the product was obtained as a gum. LC/MS System
A; R.sub.t=3.69 mins, m/z (ES.sup.+)=350 (M+H for
C.sub.21H.sub.19NO.sub.4).
(b) 4-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic acid
(4)
[0349] In an analogous manner to Example 1(b), compound (4) was
synthesised from compound (3) (72 mg, 0.206 mmoles). 51 mg of the
product was obtained as a white solid. LC/MS System C; R.sub.t=2.74
mins, m/z (ES.sup.-)=320 (M-H for C.sub.19H.sub.15NO.sub.4).
Example 3
Synthesis of
3-{4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic acid
(16)
##STR00037##
[0350] (a)
3-{4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic acid
ethyl ester (15)
[0351] In an analgous manner to Example 2(a), compound (15) was
synthesised from 5-phenyl-furan-2-carboxylic acid and
3-(4-amino-phenyl)-propionic acid ethyl ester.
(b) 3-{4-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic acid
(16)
[0352] In an analogous manner to Example 2(b), compound (16) was
synthesised from compound (15).
Example 4
Synthesis of 4-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic
acid (10)
(a) Ethyl-3-aminophenyl acetate (6)
##STR00038##
[0354] A stirred solution of 3-aminophenyl acetic acid (1 g, 6.6
mmoles) (5) and conc. sulphuric acid (2 ml) in ethanol (20 ml) was
refluxed for 3 hours. The solvent was evaporated and the residue
dissolved in ethyl acetate, washed with water, sodium carbonate,
brine, water, and finally dried (MgSO.sub.4. After concentrating in
vacuo (6) (918 mg) was obtained as dark red oil.
(b) 5-phenyl-furan-2-carboxylic acid methyl ester (7)
##STR00039##
[0356] A mixture of methyl 5-bromofuroate (1 g, 5 mmoles),
phenylboronic acid (1 g, 8.2 mmoles),
tetrakis(triphenylphosphine)palladium(0) (0.2 g, 0.17 mmoles),
sodium carbonate (1.5 g, 17.4 mmoles) in toluene (100 ml) was
refluxed for 16 hours. After cooling, the solvent was evaporated
and the yellow residue was portioned between water (50 ml) and
ethyl acetate (50 ml). The aqueous layer was extracted with ethyl
acetate (3.times.30 ml) and the combined organic layers washed with
water (1.times.30 ml) and dried (MgSO.sub.4. The residue was
purified by flash chromatography (20% ethyl acetate/70% cyclohexane
and 10% diethyl ether/90% cyclohexane) to afford (7) (384 mg). This
ester was used directly in the next step.
(c) 5-phenyl-furan-2-carboxylic acid (8)
##STR00040##
[0358] A solution of sodium hydroxide (200 mg) in water (5 ml) was
added to a stirred solution of 5-phenyl-furan-2-carboxylic acid
methyl ester (7) (384 mg, 1.90 mmoles) in methanol (20 ml) and the
mixture was stirred at room temperature for 4 hours. The solvent
was evaporated and the residue was diluted with water (10 ml) and
acidified to pH=2 with 1 M aqueous hydrochloric acid. The
precipitate was collected, washed with water and the residue was
triturated with cyclohexane to afford (8) (350 mg) as a white
solid. LC/MS System A; R.sub.t=3.89 mins.
(d) {3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester (9)
##STR00041##
[0360] In an analgous manner to Example 1(a), compound (9) was
synthesised from 5-phenyl-furan-2-carboxylic acid (8) (73.5 mg,
0.390 mmoles) and ethyl-3-aminophenyl acetate (6) (70 mg, 0.390
mmoles). 80 mg of the product was obtained as a gum. LC/MS System
D; R.sub.t=3.83 mins, m/z (ES.sup.+)=350 (M+H for
C.sub.21H.sub.19NO.sub.4).
(e) {3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acetic acid
(10)
##STR00042##
[0362] In an analogous manner to Example 1(b), compound (10) was
synthesised from compound (9) (70 mg, 0.200 mmoles). 44 mg of the
product was obtained as a white solid. LC/MS System D; R.sub.t=2.90
mins, m/z (ES.sup.-)=320 (M-H for C.sub.19H.sub.15NO.sub.4).
Example 5
Synthesis of
(3-[(5-(4-Methoxy-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic
acid (12) and
(3-[(5-(4-Dimethylamino-phenyl)-furan-2-carbonyl)-amino]-phenyl)-
-acetic acid (14)
##STR00043##
[0363] (a) (3-[(5-Bromo-furan-2-carbonyl)-amino]-phenyl)-acetic
acid ethyl ester (11)
[0364] To a solution of 5-bromo-2-furoic acid (1.14 g) and
3-aminophenylacetic acid ethyl ester (1.06 g) in anhydrous DMF (15
ml) was added diisopropylamine (2.1 ml) and then
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (2.259). The solution was stirred at room
temperature for 16 hours then partitioned between ethyl acetate and
water. The organic layer was separated, washed twice with 1M
hydrochloric acid, water, aqueous sodium carbonate solution, brine,
dried over sodium sulphate and evaporated in vacuo. Compound 11
(1.8 g) was obtained following silica gel column chromatography of
the residue in 2:1 ethyl acetate:petroleum ether.
[0365] .sup.1H NMR (CDCl.sub.3, .delta.): 1.2 (3H, t); 3.65 (2H,
s); 4.2 (2H, q); 6.5 (1H, d); 7.1 (1H, d); 7.25 (1H, d); 7.35 (1H,
t); 7.6 (2H, c); 8.0 (1H, broad s).
(b)
(3-[(5-(4-Methoxy-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic
acid (12)
[0366] (i) To a previously degassed mixture of
(3-[(5-bromo-furan-2-carbonyl)-amino]-phenyl)-acetic acid ethyl
ester (11) (0.4 g), 4-methoxyphenylboronic acid (0.19 g), potassium
carbonate (0.39 g) and tetra-n-butylammonium bromide (0.37 g) in
water (2 ml) was added palladium II acetate (circa 10 mg). The
mixture was heated to 70.degree. C. for an hour, cooled and
partitioned between ethyl acetate and water. The organic layer was
separated, washed with brine, dried over sodium sulphate and
evaporated in vacuo.
(3-[(5-(4-Methoxy-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic
acid ethyl ester (0.4 g) was obtained following silica gel column
chromatography of the residue in 2:1 ethyl acetate:petroleum
ether.
[0367] (ii) The product of the previous step was hydrolysed in IMS
(80 ml) by the addition of a solution of sodium hydroxide (0.65 g)
in water (21 ml). The resulting solution was stirred at room
temperature for 2 hours then evaporated in vacuo below 40.degree.
C. The residue was dissolved in dichloromethane, washed with 2M
hydrochloric acid and the aqueous layer back-extracted with
dichloromethane. The organic layers were combined, dried over
sodium sulphate, filtered and evaporated in vacuo. Compound 12
(0.28 g; m.p. 179-180.degree. C.) was obtained following
trituration of the residue in a mixture of dichloromethane and
pentane.
[0368] .sup.1H NMR (d.sub.6-DMSO, .delta.): 3.6 (2H, s); 3.8 (3H,
s); 7.0 (4H, c); 7.25 (1H, t); 7.4 (1H, d); 7.65 (2H, c); 7.9 (2H,
d); 10.1 (1H, s); 12.4 (1H, broad s); m/z=374.0 (M+Na).sup.+;
microanalysis for C.sub.20H.sub.17NO.sub.5. 0.25H.sub.2O: C,
expected 67.50; found 67.46; H, expected 4.96; found 4.85; N,
expected 3.94; found 3.89.
##STR00044##
(c)
(3-[(5-(4-Dimethylamino-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acet-
ic acid ethyl ester (13)
[0369] To a previously degassed mixture of
(3-[(5-bromo-furan-2-carbonyl)-amino]-phenyl)-acetic acid ethyl
ester (11) (0.4 g), 4-(dimethylamino)phenylboronic acid (0.239),
potassium carbonate (0.39 g) and tetra-n-butylammonium bromide
(0.37 g) in water (2 ml) was added palladium II acetate (circa 10
mg). The mixture was heated to 70.degree. C. for an hour, cooled
and partitioned between ethyl acetate and water. The organic layer
was separated, washed with brine, dried over sodium sulphate and
evaporated in vacuo. Compound 13(0.33 g) was obtained following
silica gel column chromatography of the residue in 2:3 ethyl
acetate:petroleum ether.
[0370] .sup.1H NMR (d.sub.6-DMSO, .delta.): 1.2 (3H, t); 2.95 (6H,
s); 3.6 (2H, s); 4.1 (2H, q); 6.75 (2H, d); 6.85 (1H, d); 7.0 (1H,
m); 7.3 (1H, t); 7.35 (1H, d); 7.65 (2H, c); 7.8 (2H, d); 10.05
(1H, s).
(d)
(3-[(5-(4-Dimethylamino-phenyl)-furan-2-carbonyl)-amino]-phenyl)-aceti-
c acid (14)
[0371] To a solution of
(3-[(5-(4-dimethylamino-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic
acid ethyl ester (13) (0.33 g) in IMS (80 ml) was added a solution
of sodium hydroxide (0.65 g) in water (21 ml). The resulting
solution was stirred at room temperature for 1 hour then
concentrated in vacuo below 40.degree. C. to circa 15 ml volume.
Water (50 ml) then acetic acid (1.5 ml) were added and the
resulting precipitate filtered, washed with water and triturated
with dichloromethane/pentane to yield the title compound (0.26 g;
m.p. 187-190.degree. C.).
[0372] .sup.1H NMR (d.sub.6-DMSO, .delta.): 2.95 (6H, s); 3.6 (2H,
s); 6.75 (2H, d); 6.85 (1H, d); 7.0 (1H, m); 7.3 (1H, t); 7.35 (1H,
d); 7.65 (2H, c); 7.8 (2H, d); 10.05 (1H, s); m/z=387.1
(M+Na).sup.+; microanalysis for
C.sub.21H.sub.20N.sub.2O.sub.4.0.2H.sub.2O: C, expected 68.54;
found 68.77; H, expected 5.59; found 5.83; N, expected 7.61; found
7.26.
General Experimental Details for Examples 6 to 8
[0373] Commercially available reagents and solvents (HPLC grade)
were used without further purification.
[0374] Microwave irradiation was carried out using a CEM Discover
focused microwave reactor.
[0375] .sup.1H NMR spectra were recorded on a Bruker 400 MHz AV
spectrometer in deuterated solvents. Chemical shifts (.delta.) are
in parts per million and coupling constants are expressed in Hz.
Thin-layer chromatography (TLC) analysis was performed with
Kieselgel 60 F.sub.254 (Merck) plates and visualized using UV
light.
[0376] Analytical HPLC-MS was performed on Agilent HP1100, Waters
600 or Waters 1525 LC systems using reverse phase Hypersil BDS C18
columns (5 .mu.m, 2.1.times.50 mm), gradient 0-95% B (A=water/0.1%
TFA, B=acetonitrile/0.1% TFA) over 2.10 min, flow=1.0 ml/min. UV
spectra were recorded at 215 nm using a Gilson G1315A Diode Array
Detector, G1214A single wavelength UV detector, Waters 2487 dual
wavelength UV detector, Waters 2488 dual wavelength UV detector, or
Waters 2996 diode array UV detector. Mass spectra were obtained
over the range m/z 150 to 850 at a sampling rate of 2 scans per
second or 1 scan per 1.2 seconds using Micromass LCT with Z-spray
interface or Micromass LCT with Z-spray or MUX interface. Data were
integrated and reported using OpenLynx and OpenLynx Browser
software.
[0377] Purification of compounds by preparative HPLC was performed
on Gilson systems using reverse phase ThermoHypersil-Keystone
Hyperprep HS C18 columns (12 .mu.m, 100.times.21.2 mm), gradient
20-100% B (A=water/0.1% TFA, B=acetonitrile/0.1% TFA) over 9.5 min,
flow=30 ml/min, injection solvent 2:1 DMSO:acetonitrile (1.6 ml),
UV detection at 215 nm.
Common Methods
[0378] In the following examples, the following common methods A to
J are employed.
##STR00045##
[0379] Thionyl chloride (1 eq) was added dropwise to MeOH (15 vol)
at 0.degree. C. followed 10 min later by careful addition of a
solution of carboxylic acid (1 eq) in MeOH (5 vol) at 0.degree. C.
The reaction mixture was allowed to warm to room temperature then
stirred for 3 h. The reaction mixture was evaporated in vacuo to
give the ester.
##STR00046##
[0380] A solution of carboxylic acid (1 eq) was heated under reflux
for 18 h with H.sub.2SO.sub.4 (0.5 vol) in MeOH or EtOH (25 vol).
The solvent was evaporated in vacuo and the residue partitioned
between DCM and aqueous sodium bicarbonate. The DCM layer was
washed with brine, dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo to give the ester.
##STR00047##
[0381] To a stirred solution of carboxylic acid (1 eq) and amino
acid ester (1 eq) in DMF (20 vol) was added DIPEA (1 eq) followed
by TBTU (1 eq). The reaction was stirred overnight, or until
complete by LC/MS, at room temperature. To the reaction mixture was
added EtOAc (30 vol) and the organic layer was washed with 2M HCl
(2.times.50 vol), brine (2.times.50 vol), saturated aqueous
NaHCO.sub.3 (2.times.50 vol) and brine (2.times.50 vol). The
organic layer was dried (MgSO.sub.4), filtered and the solvent
removed in vacuo to give the product.
##STR00048##
[0382] The carboxylic acid (1 eq), EDC (1.2 eq), and HOAt (1.2 eq)
were added to a vial as solids. The amino ester was dissolved in
DMF (10 vol) and added to the vial. The reaction was stirred at
room temperature overnight or until complete by LC/MS. Water (20
vol) was added and the mixture was extracted with and EtOAc
(3.times.10 vol). The organic layer was then washed with water (10
vol), dried (MgSO.sub.4), filtered and concentrated in vacuo.
Column chromatography using a stepped gradient of EtOAc in heptane
gave the product.
##STR00049##
To a suspension of the aryl bromide (1 eq), Cs.sub.2CO.sub.3 (1.2
eq) and boronic acid (1.1 eq) in toluene (15 vol) and MeOH (4 vol)
was added Pd(PPh.sub.3).sub.4 (0.1 eq). The resulting mixture was
heated in a CEM discover microwave for 30 mins at 120.degree. C.
(150 W, 250 psi). Analysis was carried out by LC-MS and, if
required, the reaction was heated again to drive the reaction to
completion. Once complete, the reaction mixture was filtered
through celite and the solvents removed in vacuo. The crude residue
was re-dissolved in EtOAc and washed with water (3.times.5 vol).
The combined organic layers were dried (Na.sub.2SO.sub.4), filtered
and the solvents removed in vacuo. The compounds were then purified
by column chromatography.
[0383] If the ester group present was ethyl ester then EtOH was
used instead of MeOH
[0384] E1) In some cases, LC-MS analysis showed that partial
hydrolysis occurred during reaction. In this case, after the
solvents were removed in vacuo, the residue was re-dissolved in
EtOAc (1.5 vol) and the organic layer was washed with 1M HCl
(2.times.1 vol), dried (Na.sub.2SO.sub.4), filtered and the solvent
removed in vacuo. The residue was triturated with TBME (1.5
vol).
##STR00050##
[0385] To a suspension of the aryl bromide (1.2 eq),
Cs.sub.2CO.sub.2 (4.0 eq) and boronic acid (1 eq) in toluene (5
vol) and EtOH (5 vol) under N.sub.2 was added Pd(PPh.sub.3).sub.4
(0.05 eq) and the resulting mixture was heated to 85.degree. C. for
3 h. The solvents were removed in vacuo and the solids re-suspended
in EtOAc (10 vol). Water (10 vol) was then added and all the solids
dissolved. The layers were separated and the aqueous layer was
washed with EtOAc (3.times.5 vol) and acidified to pH 4 with 2M HCl
upon which a precipitate formed. This was then extracted with EtOAc
(2.times.10 vol). The combined organic layers were dried
(Na.sub.2SO.sub.4) and removed in vacuo to give the product.
##STR00051##
To a solution of the ester in THF (1.5 ml) was added NaOH (18 eq)
in water (0.5 ml) and the resulting solution was stirred for 1 h at
room temperature. The THF was removed under a stream of N.sub.2
then EtOAc (2 ml) and water (1 ml) were added. The aqueous layer
was extracted with EtOAc (2.times.2 ml) and acidified with 2M HCl
until a white precipitate formed. This was then extracted with
EtOAc (3.times.2 ml). The solvent was removed in vacuo to give the
product.
##STR00052##
[0386] To a solution of ethyl ester in EtOH (2 ml) was added 1M
NaOH (2 ml) and the resulting solution was stirred for 30 min at
room temperature. The EtOH was then removed in vacuo and the
residue re-dissolved in TBME (20 ml) and water (20 ml). The aqueous
layer was extracted with TBME (2.times.20 ml) then acidified with
2M HCl until a white precipitate formed. This was then extracted
with EtOAc (3.times.20 ml). The combined organic layers were washed
with brine, dried (Na.sub.2SO.sub.4), filtered and the solvent
removed in vacuo to give the product.
##STR00053##
[0387] The nitro ester was dissolved in EtOH (6 vol) and
NH.sub.4COOH (4 eq) was added as a solid. 5% Palladium on carbon
(10% by weight) was then added under N.sub.2 and the resulting
mixture heated to reflux under N.sub.2 for 30 min. The reaction
mixture was filtered through celite and the celite was washed with
EtOH (20 vol). The solvent was removed in vacuo to give the
product.
##STR00054##
[0388] The nitro derivative was dissolved in EtOH (5 vol) and
SnCl.sub.2.2H.sub.2O (50 eq) was added as a solid. The resulting
solution was then stirred at 60.degree. C. for 2 h. After cooling
to room temperature, a pre-mixed solution of saturated Rochelle's
salt (10 vol) and saturated NaHCO.sub.3 (10 vol) was added to the
reaction mixture and the aqueous layer was extracted with EtOAc
(3.times.20 vol). The combined organic layers were dried
(MgSO.sub.4) and the solvent removed in vacuo to afford the
product.
##STR00055##
[0389] To a solution of nitrile (1 eq) in toluene (4 vol) was added
Me.sub.3SnN.sub.3 (1.1 eq). After heating to reflux for 18 h,
analysis was carried out by LC-MS. If required, additional
Me.sub.3SnN.sub.3 (1.1 eq) and toluene (3 vol) were added and the
reaction heated again to drive the reaction to completion. 2M NaOH
(3 vol) and hexane (3 vol) were then added to the reaction mixture
and stirred for 10 min. Water (1.5 vol) was added and the organic
layer separated. EtOAc (3 vol) was added to the aqueous layer and
the solution stirred for 2 min before the organic layer was
separated. The combined organic layers were discarded. The aqueous
layer was then acidified to pH 5 with 2M HCl then EtOAc (3.5 vol)
was added and the solution stirred for 10 min after which time the
organic layer was separated. Further EtOAc (3.5 vol) was added to
the aqueous layer and the solution stirred for 1 hour. The EtOAc
layer was separated and these combined organic layers were
evaporated in vacuo.
##STR00056##
[0390] To a suspension of the nitrile (1 eq) in DME (2 vol) were
added TMSN.sub.3 (4 eq) and Bu.sub.2SnO (0.2 eq). The resulting
mixture was heated in a CEM Discover microwave for 40 min at
150.degree. C. (150 W, 250 psi). Analysis was carried out by LC-MS
and, if required, the mixture was heated again to drive the
reaction to completion. Once complete, EtOAc (3.5 vol) and H.sub.2O
(3.5 vol) were added. The layers were separated, and the organic
layer was washed with a saturated NaHCO.sub.3 solution (3.times.3.5
vol). The aqueous layer was acidified with 2M HCl until a white
precipitate appeared, then extracted with EtOAc (3.times.3.5 vol).
The solvent was removed under a stream of N.sub.2.
##STR00057##
[0391] To a solution of ester in EtOH or MeOH (5 vol), water (5
vol) and THF (10 vol) was added LiOH (20 eq.) and the resulting
solution was stirred for 4 h at room temperature. ROH and THF were
removed under a stream of N.sub.2 and the remaining aqueous layer
acidified using 1M HCl until a white precipitate appeared. The
aqueous layer was then extracted using EtOAc (2.times.20 vol). This
organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo.
Example 6
a)
(3-{[5-(2-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (17)
(i) (3-Amino-phenyl)-acetic acid methyl ester (15)
##STR00058##
[0393] 3-Aminophenylacetic acid (5 g, 33.1 mmol) was esterified
with MeOH using Method B to give the title compound
[0394] Yield: 4.22 g, 77%; LC/MS t.sub.r 0.70 min; MS(ES+) m/z 166
(M+H).
(ii) {3-[(5-Bromo-furan-2-carbonyl)-amino]-phenyl}-acetic acid
methyl ester (16)
##STR00059##
[0396] Methyl ester (15) (1 g, 6.06 mmol) was coupled to
5-bromo-furan-2-carboxylic acid (1.16 g, 6.07 mmol) using Method C
to give the title compound
[0397] Yield: 1.83 g, 89%; LC/MS t.sub.r 1.34 min; MS(ES+) m/z 338,
340 (M+H).
(iii)
(3-{[5-(2-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00060##
[0399] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
2-methoxy-phenylboronic acid (49 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0400] Yield: 18 mg, 17%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 366
(M+H).
(iv)
(3-{[5-(2-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (17)
##STR00061##
[0402] The ester (18.4 mg, 0.050 mmol) was hydrolysed with NaOH (36
mg, 0.9 mmol) using Method G to give the title compound.
[0403] Yield: 5.6 mg, 32%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 352
(M+H); HPLC Purity: 99%; .sup.1H NMR (250 MHz; MeOD): .delta. 3.65
(s, 2H), 4.05 (s, 3H), 7.1-7.2 (m, 4H), 7.3-7.45 (m, 3H), 7.65-7.75
(m, 2H), 8.25 (s, 1H).
b)
(3-{[5-(3-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (18)
(i)
(3-{[5-(3-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00062##
[0405] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-methoxy-phenylboronic acid (49 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0406] Yield: 13 mg, 12%; LC/MS t.sub.r 1.48 min; MS(ES+) m/z 366
(M+H).
(ii)
(3-{[5-(3-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (18)
##STR00063##
[0408] The ester (13 mg, 0.035 mmol) was hydrolysed with NaOH (25
mg, 0.63 mmol using Method G to give the title compound.
[0409] Yield: 8.2 mg, 66%; LC/MS t.sub.r 1.41 min; MS(ES+) m/z 352
(M+H); HPLC Purity: 99%; .sup.1H NMR (250 MHz; MeOD): .delta. 3.70
(s, 2H), 3.95 (s, 3H), 6.95-7.05 (m, 2H), 7.10-7.15 (m, 1H),
7.3-7.45 (m, 3H), 7.50-7.6 (m, 2H), 7.65-7.75 (m, 2H).
c) (3-{[5-(3-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (19)
(i)
(3-{[5-(3-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00064##
[0411] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-acetyl-phenylboronic acid (53 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0412] Yield: 11 mg, 10%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 378
(M+H).
(ii)
(3-{[5-(3-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (19)
##STR00065##
[0414] The ester (11 mg, 0.028 mmol) was hydrolysed with NaOH (20
mg, 0.5 mmol) using Method G to give the title compound.
[0415] Yield: 10 mg, 98%; LC/MS t.sub.r 1.34 min; MS(ES+) m/z 364
(M+H).
[0416] HPLC Purity: 92%; .sup.1H NMR (250 MHz; MeOD): .delta. 2.5
(s, 3H), 3.45 (s, 2H), 6.9 (s, 2H), 7.10-7.20 (m, 2H), 7.35-7.5 (m,
3H), 7.8 (d, 1H), 7.95 (d, 1H), 8.35 (s, 1H).
d) (3-{[5-(4-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (20)
(1)
(3-{[5-(4-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00066##
[0418] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
4-acetyl-phenylboronic acid (53 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0419] Yield: 26 mg, 23%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 378
(M+H).
(ii)
(3-{[5-(4-Acetyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (20)
##STR00067##
[0421] The ester (26 mg, 0.068 mmol) was hydrolysed with NaOH (49
mg, 1.22 mmol) using Method G to give the title compound.
[0422] Yield: 22 mg, 87%; LC/MS t.sub.r 1.35 min; MS(ES+) m/z 364
(M+H).
[0423] HPLC Purity: 87%; .sup.1H NMR (400 MHz; MeOD): .delta. 2.6
(s, 3H), 3.65 (s, 2H), 7.10-7.20 (m, 2H), 7.30-7.40 (m, 2H), 7.70
(s, 2H), 8.05-8.10 (m, 4H).
(e)
(3-{[5-(3-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (21)
(i)
(3-{[5-(3-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00068##
[0425] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-methyl-phenylboronic acid (44 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0426] Yield: 20 mg, 19%; LC/MS t.sub.r 1.59 min; MS(ES+) m/z 350
(M+H).
(ii)
(3-{[5-(3-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (21)
##STR00069##
[0428] The ester (20 mg, 0.057 mmol) was hydrolysed with NaOH (41
mg, 1.03 mmol) using Method G to give the title compound.
[0429] Yield: 15 mg, 78%; LC/MS t.sub.r 1.41 min; MS(ES+) m/z 336
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 2.35
(s, 3H), 3.5 (s, 2H); 6.9 (s, 1H), 7.0-7.05 (m, 1H), 7.1-7.15 (m,
1H), 7.20-7.30 (m, 3H), 7.5 (s, 1H), 7.60-7.65 (m, 2H), 7.7 (s,
1H).
(f)
(3-{[5-(4-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (22)
(i)
(3-{[5-(4-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00070##
[0431] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
4-methyl-phenylboronic acid (44 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0432] Yield: 45 mg, 44%; LC/MS t.sub.r 1.60 min; MS(ES+) m/z 350
(M+H).
(ii)
(3-{[5-(4-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (22)
##STR00071##
[0434] The ester (45 mg, 0.13 mmol) was hydrolysed with NaOH (94
mg, 2.34 mmol) using Method G.
[0435] Yield: 36 mg, 84%; LC/MS t.sub.r 1.41 min; MS(ES+) m/z 336
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 2.2
(s, 3H), 3.45 (s, 2H), 6.7 (d, 1H), 6.9 (d, 1H), 7.05-7.15 (m, 4H),
7.45-7.50 (m, 2H), 7.65 (d, 2H).
(g)
(3-{[5-(2-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ace-
tic acid (23)
(i)
(3-{[5-(2-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ace-
tic acid methyl ester
##STR00072##
[0437] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
2-trifluoromethyl-phenylboronic acid (44 mg, 0.33 mmol) using
Method E. The crude compound was purified by column chromatography,
eluting in 17% EtOAc in heptane to give the title compound.
[0438] Yield: 55 mg, 46%; LC/MS t.sub.r 1.62 min; MS(ES+) m/z 404
(M+H).
(ii)
(3-{[5-(2-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ac-
etic acid (23)
##STR00073##
[0440] The ester (55 mg, 0.14 mmol) was hydrolysed with NaOH (100
mg, 2.52 mmol) using Method G to give the title compound.
[0441] Yield: 47 mg, 89%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 390
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 3.8
(s, 2H), 7.05-7.10 (m, 1H), 7.25-7.30 (m, 1H), 7.45-7.60 (m, 2H),
7.75-7.85 (m, 3H), 7.90-7.95 (m, 1H), 8.00-8.05 (m, 1H), 8.15-8.2
(m, 1H).
(h)
(3-{[5-(3-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ace-
tic acid (24)
(i)
(3-{[5-(3-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ace-
tic acid methyl ester
##STR00074##
[0443] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-trifluoromethyl-phenylboronic acid (44 mg, 0.33 mmol) using
Method E. The crude compound was purified by column chromatography,
eluting in 17% EtOAc in heptane to give the title compound.
[0444] Yield: 30 mg, 25%; LC/MS t.sub.r 1.65 min; MS(ES+) m/z 404
(M+H).
(ii)
(3-{[5-(3-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ac-
etic acid (24)
##STR00075##
[0446] The ester (30 mg, 0.074 mmol) was hydrolysed with NaOH (53
mg, 1.33 mmol) using Method G to give the title compound.
[0447] Yield: 25 mg, 87%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 390
(M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz; MeOD): .delta. 3.45
(s, 2H), 7.00-7.05 (m, 2H), 7.15-7.20 (m, 1H), 7.3 (d, 1H), 7.45
(s, 1H), 7.55-7.60 (m, 3H), 8.05-8.10 (m, 1H), 8.25 (s, 1H).
(j)
(3-{[5-(2,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (25)
(i)
(3-{[5-(2,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00076##
[0449] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
2,4-dichloro-phenylboronic acid (61 mg, 0.33 mmol) using Method E.
The crude compound was purified by column chromatography, eluting
in 17% EtOAc in heptane to give the title compound.
[0450] Yield: 37 mg, 31%; LC/MS t.sub.r 1.76 min; MS(ES+) m/z 404,
406 (M+H).
(ii)
(3-{[5-(2,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (25)
##STR00077##
[0452] The ester (37 mg, 0.091 mmol) was hydrolysed with NaOH (66
mg, 1.64 mmol) using Method G to give the title compound.
[0453] Yield: 9.1 mg, 25%; LC/MS t.sub.r 1.96 min; MS(ES+) m/z 390,
392 (M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta.
3.5 (s, 2H), 7.0 (d, 1H), 7.2-7.25 (m, 2H), 7.3 (d, 1H), 7.4 (d,
1H), 7.5 (s, 1H), 7.6 (2H), 8.1 (1H).
(k)
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (26)
(i)
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00078##
[0455] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3,5-dichloro-phenylboronic acid (61 mg, 0.33 mmol) using Method E.
The crude compound was purified by column chromatography, eluting
in 17% EtOAc in heptane to give the title compound.
[0456] Yield: 11 mg, 9%; LC/MS t.sub.r 1.76 min; MS(ES+) m/z 404,
406 (M+H).
(ii)
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (26)
##STR00079##
[0458] The ester (11 mg, 0.027 mmol) was hydrolysed with NaOH (20
mg, 0.49 mmol) using Method G to give the title compound.
[0459] Yield: 9.6 mg, 91%; LC/MS t.sub.r 1.97 min; MS(ES+) m/z 390,
392 (M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta.
3.55 (s, 2H), 7.00-7.05 (m, 2H), 7.20-7.30 (m, 2H), 7.35 (s, 1H),
7.55-7.60 (m, 2H), 7.9 (s, 2H).
(l)
(3-{[5-(3,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (27)
(i)
(3-{[5-(3,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00080##
[0461] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3,4-dichloro-phenylboronic acid (61 mg, 0.33 mmol) using Method E.
The crude compound was purified by column chromatography, eluting
in 17% EtOAc in heptane to give the title compound.
[0462] Yield: 33 mg, 27%; LC/MS t.sub.r 1.70 min; MS(ES+) m/z 404,
406 (M+H).
(ii)
(3-{[5-(3,4-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (27)
##STR00081##
[0464] The ester (33 mg, 0.081 mmol) was hydrolysed with NaOH (58
mg, 1.46 mmol) using Method G to give the title compound.
[0465] Yield: 24 mg, 76%; LC/MS t.sub.r 1.92 min; MS(ES+) m/z 390,
392 (M+H); HPLC Purity: 87%; .sup.1H NMR (400 MHz; MeOD): .delta.
3.5 (s, 2H), 6.95-7.05 (m, 2H), 7.20-7.25 (m, 2H), 7.45-7.50 (m,
1H), 7.55-7.60 (m, 2H), 7.7 (d, 1H), 8.1 (s, 1H).
(m)
(3-{[5-(2-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (28)
(i)
(3-{[5-(2-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00082##
[0467] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
2-methyl-phenylboronic acid (44 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0468] Yield: 60 mg, 58%; LC/MS t.sub.r: 1.55 min; MS(ES+) m/z 350
(M+H).
(ii)
(3-{[5-(2-Methyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (28)
##STR00083##
[0470] The ester (60 mg, 0.17 mmol) was hydrolysed with NaOH (122
mg, 3.06 mmol) using Method G to give the title compound.
[0471] Yield: 41 mg, 71%; LC/MS t.sub.r 1.84 min; MS(ES+) m/z 336
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 2.4
(s, 3H), 3.5 (s, 2H), 6.7 (d, 1H), 7.0 (d, 1H), 7.15-7.20 (m, 4H),
7.28-7.30 (m, 1H), 7.50-7.60 (m, 2H), 7.75-7.85 (m, 1H).
(n)
(3-{[5-(4-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (29)
(i)
(3-{[5-(4-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00084##
[0473] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
4-methoxy-phenylboronic acid (49 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0474] Yield: 50 mg, 46%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 366
(M+H).
(ii)
(3-{[5-(4-Methoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (29)
##STR00085##
[0476] The ester (50 mg, 0.14 mmol) was hydrolysed with NaOH (100
mg, 2.52 mmol) using Method G to give the title compound.
[0477] Yield: 45 mg, 93%; LC/MS t.sub.r 1.79 min; MS(ES+) m/z 352
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 3.5
(s, 2H), 3.7 (s, 3H), 6.7 (s, 1H), 6.9 (d, 2H), 7.0 (d, 1H),
7.20-7.25 (m, 2H), 7.55-7.60 (m, 2H), 7.70-7.80 (m, 2H).
(o)
(3-{[5-(2-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (30)
(i)
(3-{[5-(2-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00086##
[0479] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
2-chloro-phenylboronic acid (51 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0480] Yield: 38 mg, 34%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 370,
372 (M+H).
(ii)
(3-{[5-(2-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (30)
##STR00087##
[0482] The ester (38 mg, 0.10 mmol) was hydrolysed with NaOH (72
mg, 1.8 mmol) using Method G to give the title compound.
[0483] Yield: 35 mg, 95%; LC/MS t.sub.r 1.86 min; MS(ES+) m/z 356,
358 (M+H); HPLC Purity: 97%; .sup.1H NMR (400 MHz; MeOD): .delta.
3.5 (s, 2H), 6.95-7.00 (m, 1H), 7.20-7.30 (m, 4H), 7.30-7.38 (m,
1H), 7.40-7.45 (m, 1H), 7.55-7.60 (m, 2H), 8.10 (d, 1H).
(p) (3-{[5-Naphthalen-1-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid (31)
(i) (3-{[5-Naphthalen-1-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid methyl ester
##STR00088##
[0485] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
1-naphthaleneboronic acid (56 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0486] Yield: 12 mg, 10%; LC-MS t.sub.r1.62 min; MS(ES+) m/z 386
(M+H).
(ii) {3-[(5-Naphthalen-1-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid (31)
##STR00089##
[0488] The ester (12 mg, 0.031 mmol) was hydrolysed with NaOH (22
mg, 0.56 mmol) using Method G to give the title compound.
[0489] Yield: 8.7 mg, 76%; LC/MS t.sub.r 1.87 min; MS(ES+) m/z 372
(M+H); HPLC Purity: 89%; .sup.1H NMR (250 MHz; MeOD) .delta. 4.52
(s, 2H), 6.88 (d, 1H), 7.00 (d, 1H), 7.18-7.27 (t, 1H), 7.39 (d,
1H), 7.43-7.58 (m, 5H), 7.80-7.89 (m, 3H), 8.29 (d, 1H).
(q)
(3-{[5-(3-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ac-
etic acid (32)
(i)
(3-{[5-(3-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ac-
etic acid methyl ester
##STR00090##
[0491] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-(trifluoromethoxy)-phenylboronic acid (67 mg, 0.33 mmol) using
Method E. The crude compound was purified by column chromatography,
eluting in 17% EtOAc in heptane to give the title compound.
[0492] Yield: 23 mg, 18%; LC-MS t.sub.r1.63 min; MS(ES+) m/z 420
(M+H).
(ii)
(3-{[5-(3-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-a-
cetic acid (32)
##STR00091##
[0494] The ester (23 mg, 0.055 mmol) was hydrolysed with NaOH (40
mg, 0.99 mmol) using Method G to give the title compound.
[0495] Yield: 22 mg, 100%; LC/MS t.sub.r 1.90 min; MS(ES+) m/z 406
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz; MeOD) .delta. 3.66
(s, 2H), 7.10-7.16 (m, 2H), 7.28-7.40 (m, 3H), 7.59 (t, 1H),
7.67-7.73 (m, 2H), 7.90-7.98 (m, 2H).
(r)
(3-{[5-(4-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ac-
etic acid (33)
(i)
(3-{[5-(4-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-ac-
etic acid methyl ester
##STR00092##
[0497] The methyl ester (16) (100 mg, 0.30 mmol) was coupled to
4-(trifluoromethoxy)-phenylboronic acid (67 mg, 0.33 mmol) using
Method E. The crude compound was purified by column chromatography,
eluting in 17% EtOAc in heptane to give the title compound.
[0498] Yield: 65 mg, 52%; LC-MS t.sub.r1.62 min; MS(ES+) m/z 420
(M+H).
(ii)
(3-{[5-(4-Trifluoromethoxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-a-
cetic acid (33)
##STR00093##
[0500] The ester (65 mg, 0.15 mmol) was hydrolysed with NaOH (0.11
mg, 2.7 mmol) using Method G to give the title compound.
[0501] Yield: 47 mg, 75%; LC/MS t.sub.r 1.91 min; MS(ES+) m/z 406
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz; MeOD) .delta. 3.65
(s, 2H), 7.06 (d, 1H), 7.12 (d, 1H), 7.31-7.42 (m, 4H), 7.66-7.72
(m, 2H), 8.08 (d, 2H).
(s)
(3-{[5-(3-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (34)
(i)
(3-{[5-(3-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00094##
[0503] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-isopropyl-phenylboronic acid (53 mg, 0.33 mmol) using Method E.
The crude compound was purified by column chromatography, eluting
in 17% EtOAc in heptane to give the title compound.
[0504] Yield: 30 mg, 27%; LC-MS t.sub.r1.70 min; MS(ES+) m/z 378
(M+H).
(ii)
(3-{[5-(3-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (34)
##STR00095##
[0506] The ester (30 mg, 0.080 mmol) was hydrolysed with NaOH (58
mg, 1.44 mmol) using Method G to give the title compound.
[0507] Yield: 29 mg, 100%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 364
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD) .delta. 1.20
(d, 6H), 2.90 (sept, 1H), 3.53 (s, 2H), 6.87 (d, 1H), 7.00 (d, 1H),
7.17 (d, 1H), 7.20-7.29 (m, 3H), 7.52-7.59 (m, 2H), 7.63 (d, 1H),
7.72 (s, 1H).
(t)
(3-{[5-(4-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (35)
(i)
(3-{[5-(4-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00096##
[0509] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
4-isopropyl-phenylboronic acid (53 mg, 0.33 mmol) using Method E.
The crude compound was purified by column chromatography, eluting
in 17% EtOAc in heptane to give the title compound.
[0510] Yield: 33 mg, 30%; LC-MS t.sub.r1.70 min; MS(ES+) m/z 378
(M+H).
(ii)
(3-{[4-Isopropyl-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (35)
##STR00097##
[0512] The ester (33 mg, 0.087 mmol) was hydrolysed with NaOH (63
mg, 1.57 mmol) using Method G to give the title compound.
[0513] Yield: 32 mg, 100%; LC/MS t.sub.r 1.56 min; MS(ES+) m/z 364
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD) .delta. 1.19
(d, 6H), 2.86 (sept, 1H), 3.52 (s, 2H), 6.82 (d, 1H), 7.00 (d, 1H),
7.18-7.27 (m, 4H), 7.53-7.60 (m, 2H), 7.75 (d, 2H).
(u)
{3-[(5-Benzo[1,3]dioxol-5-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid (36)
(i)
{3-[(5-Benzo[1,3]dioxol-5-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid methyl ester
##STR00098##
[0515] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3,4-(methylenedioxy)-phenylboronic acid (54 mg, 0.33 mmol) using
Method E. The crude compound was purified by column chromatography,
eluting in 17% EtOAc in heptane to give the title compound.
[0516] Yield: 25 mg, 22%; LC-MS t.sub.r1.46 min; MS(ES+) m/z 380
(M+H).
(ii)
{3-[(5-Benzo[1,3]dioxol-5-yl-furan-2-carbonyl)-amino]-phenyl}-acetic
acid (36)
##STR00099##
[0518] The ester (25 mg, 0.066 mmol) was hydrolysed with NaOH (48
mg, 1.19 mmol) using Method G to give the title compound.
[0519] Yield: 16 mg, 66%; LC/MS t.sub.r: 1.32 min; MS(ES+) m/z 366
(M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz; MeOD) .delta. 3.67
(s, 2H), 6.03 (s, 2H), 6.85 (d, 1H), 6.93 (d, 1H), 7.12 (d, 1H),
7.31-7.39 (m, 2H), 7.45-7.51 (m, 2H), 7.65-7.72 (m, 2H).
(v)
(3-{[5-(2,3-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (37)
(i)
(3-{[5-(2,3-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00100##
[0521] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
2,3-dichloro-phenylboronic acid (62 mg, 0.33 mmol) using Method E.
The crude compound was purified by column chromatography, eluting
in 17% EtOAc in heptane to give the title compound.
[0522] Yield: 15 mg, 13%; LC-MS t.sub.r1.72 min; MS(ES+) m/z 404,
406 (M+H).
(ii)
(3-{[5-(2,3-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (37)
##STR00101##
[0524] The ester (15 mg, 0.037 mmol) was hydrolysed with NaOH (27
mg, 0.67 mmol) using Method G to give the title compound.
[0525] Yield: 12 mg, 80%; LC/MS t.sub.r 1.91 min; MS(ES+) m/z 390,
392 (M+H); HPLC Purity: 96%; .sup.1H NMR (400 MHz; MeOD) .delta.
3.54 (s, 2H), 7.01 (d, 1H), 7.20-7.28 (m, 2H), 7.29-7.37 (m, 2H),
7.49 (d, 1H), 7.53-7.59 (m, 2H), 8.03 (d, 1H).
(w) {3-[([2,2']Bifuranyl-5-carbonyl)-amino]-phenyl}-acetic acid
(38)
(i) {3-[([2,2']Bifuranyl-5-carbonyl)-amino]-phenyl}-acetic acid
methyl ester
##STR00102##
[0527] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
furan-2-boronic acid (37 mg, 0.33 mmol) using Method E. The crude
compound was purified by column chromatography, eluting in 17%
EtOAc in heptane to give the title compound.
[0528] Yield: 13 mg, 13%; LC-MS t.sub.r 1.41 min; MS(ES+) m/z 326
(M+H).
(ii) {3-[([2,2']Bifuranyl-5-carbonyl)-amino]-phenyl}-acetic acid
(38)
##STR00103##
[0530] The ester (13 mg, 0.040 mmol) was hydrolysed with NaOH (29
mg, 0.72 mmol) using Method G to give the title compound.
[0531] Yield: 11 mg, 88%; LC/MS t.sub.r 1.70 min; MS(ES+) m/z 312
(M+H); HPLC Purity: 94%; NMR (400 MHz; MeOD) 6.3.56 (s, 2H), 6.50
(d, 1H), 6.67 (d, 1H), 6.88 (d, 1H), 7.00 (d, 1H), 7.19-7.23 (m,
2H), 7.49-7.58 (m, 3H).
(x)
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (39)
(i)
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00104##
[0533] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
3-chlorophenylboronic acid (51 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0534] Yield: 29 mg, 26%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 370,
372 (M+H).
(ii)
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (39)
##STR00105##
[0536] The ester (29 mg, 0.076 mmol) was hydrolysed with NaOH (55
mg, 1.37 mmol) using Method G to give the title compound.
[0537] Yield: 27 mg, 100%; LC/MS t.sub.r 1.86 min; MS(ES+) m/z 356,
358 (M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz; MeOD): .delta.
3.66 (s, 2H), 7.06-7.14 (m, 2H), 7.32-7.49 (m, 4H), 7.69-7.70 (m,
2H), 7.86 (d, 1H), 8.07 (s, 1H).
(y)
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (40)
(i)
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00106##
[0539] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
4-chloro-phenylboronic acid (51 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
17% EtOAc in heptane to give the title compound.
[0540] Yield: 34 mg, 31%; LC/MS t.sub.r 1.59 min; MS(ES+) m/z 370,
372 (M+H).
(ii)
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (40)
##STR00107##
[0542] The ester (34 mg, 0.092 mmol) was hydrolysed with NaOH (66
mg, 1.66 mmol) using Method G to give the title compound.
[0543] Yield: 23 mg, 70%; LC/MS t.sub.r 1.86 min; MS(ES+) m/z 356,
358 (M+H); HPLC Purity: 94%; .sup.1H NMR (250 MHz; MeOD): .delta.
3.34 (s, 2H), 7.15 (d, 1H), 7.12 (d, 1H), 7.36 (m, 2H), 7.48 (m,
2H), 7.69 (m, 2H), 7.94 (m, 2H).
(z) 3-{[5-(1H-Indol-5-yl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (41)
(i) 3-{[5-(1H-Indol-5-yl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid methyl ester
##STR00108##
[0545] Methyl ester (16) (100 mg, 0.30 mmol) was coupled to
1H-indole-5-boronic acid (52 mg, 0.33 mmol) using Method E. The
crude compound was purified by column chromatography, eluting in
20% EtOAc in heptane to give the title compound.
[0546] Yield: 22 mg, 20%; LC/MS t.sub.r 1.14 min; MS(ES+) m/z 375
(M+H).
(ii) 3-{[5-(1H-Indol-5-yl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (41)
##STR00109##
[0548] The ester (22 mg, 0.059 mmol) was hydrolysed with NaOH (42
mg, 1.06 mmol) using Method G to give the title compound.
[0549] Yield: 8.8 mg, 41%; LC/MS t.sub.r 1.29 min; MS(ES+) m/z 361
(M+H); HPLC Purity: 94%; .sup.1H NMR (400 MHz; DMSO): b 3.60 (s,
2H), 6.65 (s, 1H), 7.03 (d, 2H), 7.32 (t, 1H), 7.43 (d, 2H), 7.50
(d, 1H), 7.70 (m, 3H), 8.22 (s, 1H), 10.15 (s, 1H), 11.30 (s,
1H).
(aa)
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (42)
(i) Alternate synthesis of (3-Amino-phenyl)-acetic acid ethyl ester
(6)
##STR00110##
[0551] 3-Aminophenylacetic acid (2 g, 13 mmol) was esterified with
EtOH using Method B to give the title compound.
[0552] Yield: 2.1 g, 89%; LC/MS t.sub.r 0.78 min; MS(ES+) m/z 180
(M+H).
(ii) 5-(4-Fluoro-phenyl)-furan-2-carboxylic acid (76)
##STR00111##
[0554] 4-Fluoro-phenylboronic acid (611 mg, 4.4 mmol) was coupled
to 5-bromo-2-furoic acid (1 g, 5.2 mmol) using Method F to give the
title compound.
[0555] Yield: 350 mg, 38%; LC/MS t.sub.r 1.24 min; MS(ES+) m/z 207
(M+H).
(iii)
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid ethyl ester
##STR00112##
[0557] (3-Amino-phenyl)-acetic acid ethyl ester (44 mg, 0.24 mmol)
was coupled to 5-(4-fluoro-phenyl)-furan-2-carboxylic acid (76) (50
mg, 0.24 mmol) using Method C. The crude compound was purified by
column chromatography, eluting in 20% EtOAc in heptane to give the
title compound.
[0558] Yield: 90 mg, 100%; LC/MS t.sub.r 1.59 min; MS(ES+) m/z 368
(M+H).
(iv)
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (42)
##STR00113##
[0560] To a solution of ester (90 mg, 0.25 mmol) in MeOH (0.09 ml)
was added 1M NaOH (1 ml) and the reaction mixture was stirred for 3
h at room temperature. The MeOH was evaporated under a stream of
N.sub.2. The aqueous layer was washed with DCM (0.5 ml) and
acidified to pH 4 with 2M HCl until a white precipitate formed.
This was then extracted with EtOAc (0.5 ml). The organic layer was
dried (Na.sub.2SO.sub.4), filtered, and the solvent removed in
vacuo to give the title compound.
[0561] Yield: 25 mg, 30%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 339
(M+H); HPLC Purity: 95%; .sup.1H NMR (360 MHz; MeOD): .delta. 3.53
(s, 2H), 6.84 (d, 1H), 7.00 (d, 1H), 7.10 (m, 2H), 7.23 (m, 2H),
7.56 (m, 2H), 7.87 (m, 2H).
(bb) Alternate synthesis of
(3-{[5-(phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic acid
(10)
(i) (3-{[5-(phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic acid
methyl ester
##STR00114##
[0563] Methyl ester (16) (500 mg, 1.48 mmol) was coupled to
phenylboronic acid (150 mg, 1.23 mmol) using Method E. The crude
compound was purified by column chromatography, eluting with a
stepped gradient of 20-25% EtOAc in heptane to give the title
compound.
[0564] Yield: 120 mg, 29%; LC/MS t.sub.r 1.51 min; MS(ES+) m/z 336
(M+H).
(ii) (3-{[5-(phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic acid
(10)
##STR00115##
[0566] To a solution of ester (112 mg, 0.33 mmol) in THF (1.1 ml)
was added NaOH (112 mg, 2.8 mmol) in water (1.1 ml) and the
resulting solution was stirred for 6 h at room temperature. The THF
was removed under a stream of N.sub.2 and the aqueous layer was
acidified to pH 4 using 1M HCl. The aqueous layer was extracted
with DCM (2.times.2 ml) and the combined organic layers evaporated
in vacuo to give the title compound.
[0567] Yield: 97 mg, 91%; LC/MS t.sub.r 1.36 min; MS(ES+) m/z 322
(M+H); HPLC Purity: 99%; .sup.1H NMR (360 MHz; DMSO): .delta. 3.63
(s, 2H), 7.08 (d, 1H), 7.25 (d, 2H), 7.37 (t, 1H), 7.47 (m, 2H),
7.56 (t, 2H), 7.71 (s, 1H), 7.77 (d, 2H), 8.04 (d, 2H), 10.24 (s,
1H), 12.45 (s, 1H).
Example 7
(a) {3-[(5-Phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic acid
(43)
(i) {3-[(5-Bromo-thiophene-2-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00116##
[0569] 5-Bromothiophene-2-carboxylic acid (232 mg, 1.1 mmol) was
coupled with ethyl ester (6) (201 mg, 1.1 mmol) following Method C
to give the title compound.
[0570] Yield: 220 mg, 54%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 368,
370 (M+H).
(ii) {3-[(5-Phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00117##
[0572] {3-[(5-Bromo-thiophene-2-carbonyl)-amino]-phenyl}-acetic
acid ethyl ester (220 mg, 0.60 mmol) was coupled to phenylboronic
acid using Method E except that the reaction mixture was heated at
80.degree. C. for 25 min under microwave conditions. The crude
product was purified by column chromatography using 33% EtOAc in
heptane to give the title compound.
[0573] Yield: 128 mg, 58%; LC/MS t.sub.r 1.61 min; MS(ES+) m/z 366
(M+H).
(iii) {3-[(5-Phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic
acid (43)
##STR00118##
[0575] The ethyl ester (75 mg, 0.21 mmol) was hydrolysed using
Method H to give the title compound.
[0576] Yield: 44 mg, 63%; LC/MS t.sub.r 1.50 min; MS(ES+) m/z 338
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, MeOD) .delta. 3.62
(s, 2H), 7.08-7.10 (m, 1H), 7.29-7.46 (m, 5H), 7.60-7.62 (m, 2H),
7.70-7.72 (m, 2H), 7.88 (d, 1H).
(b) {3-[(4-Chloro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(44)
(i) [3-(5-Bromo-2-chloro-benzoylamino)-phenyl]-acetic acid ethyl
ester
##STR00119##
[0578] 5-Bromo-2-chlorobenzoic acid (132 mg, 0.56 mmol) was coupled
with ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give
the title compound.
[0579] Yield: 198 mg, 89%; LC/MS t.sub.r 1.55 min; MS(ES+) m/z 396,
398 (M+H).
(ii) {3-[(4-Chloro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00120##
[0581] [3-(5-Bromo-2-chloro-benzoylamino)-phenyl]-acetic acid ethyl
ester (198 mg, 0.50 mmol) was coupled to phenylboronic acid using
Method E, except that the reaction mixture was heated at 80.degree.
C. for 25 min. The crude product was purified by column
chromatography using 20% EtOAc in heptane to give the title
compound.
[0582] Yield: 86 mg, 44%; LC/MS t.sub.r 1.66 min; MS(ES+) m/z 394,
396 (M+H).
(iii) {3-[(4-Chloro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(44)
##STR00121##
[0584] The ethyl ester (86 mg, 0.22 mmol) was hydrolysed using
Method H to give the title compound.
[0585] Yield: 62 mg, 78%; LC/MS t.sub.r 1.48 min; MS(ES+) m/z 366,
368 (M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz, MeOD) .delta.
3.65 (s, 2H), 7.13 (d, 1H), 7.33-7.50 (m, 4H), 7.58-7.82 (m,
7H).
(c) {3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acetic acid
(45)
(i) {3-[(6-Bromo-pyridine-2-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester (77)
##STR00122##
[0587] 6-Bromo-2-pyridinecarboxylic acid (113 mg, 0.56 mmol) was
coupled with ethyl ester (6) (100 mg, 0.56 mmol) following Method C
to give the title compound.
[0588] Yield: 198 mg, 97%; LC/MS t.sub.r 1.52 min; MS(ES+) m/z 363,
365 (M+H).
(ii) {3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00123##
[0590] {3-[(6-Bromo-pyridine-2-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester (77) (198 mg, 0.54 mmol) was coupled to phenylboronic
acid using Method E, except that the reaction mixture was heated at
80.degree. C. for 25 min. The crude product was purified by column
chromatography using 20% EtOAc in heptane to give the title
compound.
[0591] Yield: 129 mg, 66%; LC/MS t.sub.r 1.70 min; MS(ES+) m/z 361
(M+H).
(iii) {3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acetic acid
(45)
##STR00124##
[0593] The ethyl ester (129 mg, 0.36 mmol) was hydrolysed using
Method H to give the title compound.
[0594] Yield: 100 mg, 84%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 333
(M+H); HPLC Purity: 96%; .sup.1H NMR (400 MHz, MeOD) .delta. 3.69
(s, 2H), 7.15 (d, 1H), 7.37-7.42 (m, 1H), 7.50-7.60 (m, 3H),
7.78-7.80 (m, 2H), 8.08-8.23 (m, 5H).
(d) {3-[(6-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(46)
(i) [3-(3-Bromo-4-fluoro-benzoylamino)-phenyl]-acetic acid ethyl
ester
##STR00125##
[0596] 3-Bromo-4-fluorobenzoic acid (123 mg, 0.56 mmol) was coupled
with ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give
the title compound.
[0597] Yield: 190 mg, 89%; LC/MS t.sub.r 1.55 min; MS(ES+) m/z 380,
382 (M+H).
(ii) {3-[(6-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00126##
[0599] [3-(3-Bromo-4-fluoro-benzoylamino)-phenyl]-acetic acid ethyl
ester (190 mg, 0.50 mmol) was coupled to phenylboronic acid using
Method E, except that the reaction mixture was heated at 80.degree.
C. for 25 min. The crude product was purified by column
chromatography using 20% EtOAc in heptane to give the title
compound.
[0600] Yield: 106 mg, 56%; LC/MS t.sub.r 1.67 min; MS(ES+) m/z 378
(M+H).
(iii) {3-[(6-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(46)
##STR00127##
[0602] The ethyl ester (106 mg, 0.28 mmol) was hydrolysed using
Method H to give the title compound.
[0603] Yield: 83 mg, 84%; LC/MS t.sub.r 1.51 min; MS(ES+) m/z 350
(M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz, MeOD) .delta. 3.65
(s, 2H), 7.12 (d, 1H), 7.33-7.53 (m, 5H), 7.63-7.67 (m, 4H),
7.97-8.01 (m, 1H), 8.10-8.12 (m, 1H).
(e) {3-[(3-Methyl-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid
(47)
(i) [3-(4-Bromo-2-methyl-benzoylamino)-phenyl]-acetic acid ethyl
ester
##STR00128##
[0605] 4-Bromo-2-methylbenzoic acid (120 mg, 0.56 mmol) was coupled
with ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give
the title compound
[0606] Yield: 188 mg, 89%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 376,
378 (M+H).
(ii) {3-[(3-Methyl-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00129##
[0608] [3-(4-Bromo-2-methyl-benzoylamino)-phenyl]-acetic acid ethyl
ester (188 mg, 0.50 mmol) was coupled to phenylboronic acid using
Method E, except that the reaction mixture was heated at 80.degree.
C. The crude residue was purified by column chromatography using
20% EtOAc in heptane to give the title compound.
[0609] Yield: 87 mg, 47%; LC/MS t.sub.r 1.73 min; MS(ES+) m/z 374
(M+H).
(iii) {3-[(3-Methyl-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid
(47)
##STR00130##
[0611] The ethyl ester (87 mg, 0.23 mmol) was hydrolysed using
Method H to give the title compound.
[0612] Yield: 52 mg, 65%; LC/MS t.sub.r 1.84 min; MS(ES+) m/z 346
(M+H); HPLC Purity: 96%; .sup.1H NMR (400 MHz, MeOD) .delta. 2.56
(s, 3H), 3.64 (s, 2H), 7.13 (d, 1H), 7.33-7.41 (m, 2H), 7.46-7.51
(m, 2H), 7.58-7.69 (m, 7H).
(f) {3-[(3-Chloro-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid
(48)
(i) [3-(4-Bromo-2-chloro-benzoylamino)-phenyl]-acetic acid ethyl
ester
##STR00131##
[0614] 4-Bromo-2-chlorobenzoic acid (132 mg, 0.56 mmol) was coupled
with ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give
the title compound.
[0615] Yield: 198 mg, 89%; LC/MS t.sub.r 1.57 min; MS(ES+) m/z 396,
398 (M+H).
(ii) {3-[(3-Chloro-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00132##
[0617] [3-(4-Bromo-2-chloro-benzoylamino)-phenyl]-acetic acid ethyl
ester (198 mg, 0.50 mmol) was coupled to phenylboronic acid using
Method E, except that the reaction mixture was heated at 80.degree.
C. The crude residue was purified by column chromatography using
20% EtOAc in heptane to give the title compound.
[0618] Yield: 100 mg, 51%; LC/MS t.sub.r 1.67 min; MS(ES+) m/z 394,
396 (M+H).
(iii) {3-[(3-Chloro-biphenyl-4-carbonyl)-amino]-phenyl}-acetic acid
(48)
##STR00133##
[0620] The ethyl ester (100 mg, 0.25 mmol) was hydrolysed using
Method H to give the title compound.
[0621] Yield: 90 mg, 97%; LC/MS t.sub.r 1.84 min; MS(ES+) m/z 366,
368 (M+H); HPLC Purity: 96%; .sup.1H NMR (250 MHz, MeOD) .delta.
3.64 (s, 2H), 7.13 (d, 1H), 7.32-7.55 (m, 4H), 7.64-7.79 (m,
7H).
(g) {3-[(Biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid (49)
(i) [3-(3-Bromo-benzoylamino)-phenyl]-acetic acid ethyl ester
##STR00134##
[0623] 3-Bromo-benzoic acid (112 mg, 0.56 mmol) was coupled with
ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give the
title compound.
[0624] Yield: 203 mg, 100%; LC/MS t.sub.r 1.56 min; MS(ES+) m/z
362, 364 (M+H).
(ii) {3-[(Biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid ethyl
ester
##STR00135##
[0626] [3-(3-Bromo-benzoylamino)-phenyl]-acetic acid ethyl ester
(203 mg, 0.56 mmol) was coupled to phenylboronic acid using Method
E, except that the reaction mixture was heated at 80.degree. C. The
crude residue was purified by column chromatography using 20% EtOAc
in heptane to give the title compound.
[0627] Yield: 142 mg, 70%; LC/MS t.sub.r 1.65 min; MS(ES+) m/z 360
(M+H).
(iii) {3-[(Biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid (49)
##STR00136##
[0629] The ethyl ester (140 mg, 0.39 mmol) was hydrolysed using
Method H to give the title compound.
[0630] Yield: 85 mg, 66%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 332
(M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz, MeOD) .delta. 3.65
(s, 2H), 7.13 (d, 1H), 7.32-7.44 (m, 2H), 7.47-7.54 (m, 2H),
7.59-7.75 (m, 5H), 7.85-7.96 (m, 2H), 8.21-8.22 (m, 1H).
(h)
{3-[(4-Methyl-5-phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic
acid (50)
(i) 4-Methyl-5-phenyl-thiophene-2-carboxylic acid (methyl and
ethyl) ester
##STR00137##
[0632] 5-Bromo-4-methyl-thiophene-2-carboxylic acid methyl ester
(120 mg, 0.51 mmol) was coupled to phenylboronic acid using Method
E, except that the reaction mixture was heated at 80.degree. C. in
EtOH/toluene. The crude residue was purified by column
chromatography using 10% EtOAc in heptane to give the title
compound as a mixture of the methyl and ethyl esters.
[0633] Yield: 108 mg (combined); LC/MS t.sub.r: 1.69 min (Me), 1.78
min (Et); MS(ES+) m/z 233 [(M+H) Me]; 247 [(M+H) Et]; HPLC Purity:
98% (59% Me, 39% Et).
(ii) 4-Methyl-5-phenyl-thiophene-2-carboxylic acid
##STR00138##
[0635] To a solution of 4-methyl-5-phenyl-thiophene-2-carboxylic
acid (methyl and ethyl) ester (106 mg, .about.0.45 mmol) in MeOH (5
ml) was added 1M NaOH (5 ml) and the resulting solution was stirred
for 30 min at room temperature. The MeOH was then removed in vacuo.
DCM (20 ml) and water (20 ml) were added and the aqueous layer
extracted with DCM (2.times.20 ml). The aqueous layer was acidified
with 2M HCl until a white precipitate formed. This was then
extracted with EtOAc (3.times.20 ml). The combined organic layers
were washed with brine (20 ml), dried (Na.sub.2SO.sub.4), filtered
and the solvent removed in vacuo to give the title compound.
[0636] Yield: 25 mg, 25%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 260
(M+H+MeCN).
(iii)
{3-[(4-Methyl-5-phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic
acid ethyl ester
##STR00139##
[0638] 4-Methyl-5-phenyl-thiophene-2-carboxylic acid (25 mg, 0.11
mmol) was coupled with ethyl ester (4) (20 mg, 0.11 mmol) following
Method C. The crude residue was purified by column chromatography
using 20% EtOAc in heptane to give the title compound.
[0639] Yield: 29 mg, 67%; LC/MS t.sub.r 1.70 min; MS(ES+) m/z 380
(M+H).
(iv)
{3-[(4-Methyl-5-phenyl-thiophene-2-carbonyl)-amino]-phenyl}-acetic
acid (50)
##STR00140##
[0641] The ethyl ester (29 mg, 0.08 mmol) was hydrolysed using
Method H to give the title compound.
[0642] Yield: 24 mg, 85%; LC/MS t.sub.r 1.55 min; MS(ES+) m/z 352
(M+H); HPLC Purity: 84%; .sup.1H NMR (250 MHz, MeOD) .delta. 2.38
(s, 3H), 3.62 (s, 2H), 7.12 (d, 1H), 7.30-7.60 (m, 7H), 7.64-7.67
(m, 1H), 7.77 (s, 1H).
(j) {3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(51)
(i) [3-(5-Bromo-2-fluoro-benzoylamino)-phenyl]-acetic acid ethyl
ester (78)
##STR00141##
[0644] 2-Fluoro-5-bromobenzoic acid (123 mg, 0.56 mmol) was coupled
with ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give
the title compound.
[0645] Yield: 209 mg, 98%; LC/MS t.sub.r 1.63 min; MS(ES+) m/z 380,
382 (M+H).
(ii) {3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00142##
[0647] [3-(5-Bromo-2-fluoro-benzoylamino)-phenyl]-acetic acid ethyl
ester (78) (209 mg, 0.55 mmol) was coupled to phenylboronic acid
using Method E, except that the reaction mixture was heated at
80.degree. C. The crude reside was purified by column
chromatography using 20% EtOAc in heptane to give the title
compound.
[0648] Yield: 98 mg, 47%; LC/MS t.sub.r 1.71 min; MS(ES+) m/z 378
(M+H).
(iii) {3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(51)
##STR00143##
[0650] The ethyl ester (98 mg, 0.26 mmol) was hydrolysed using
Method H to give the title compound.
[0651] Yield: 89 mg, 98%; LC/MS t.sub.r: 1.47 min; MS(ES+) m/z 350
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 3.55
(s, 2H), 7.16 (d, 1H), 7.28-7.35 (m, 1H), 7.40-7.55 (m, 4H),
7.60-7.78 (m, 5H) 8.07-8.08 (m, 1H).
(k) ({3-[(5-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(52)
(i) [3-(3-Bromo-5-fluoro-benzoylamino)-phenyl]-acetic acid ethyl
ester
##STR00144##
[0653] 3-Fluoro-5-bromobenzoic acid (123 mg, 0.56 mmol) was coupled
with ethyl ester (6) (100 mg, 0.56 mmol) following Method C to give
the title compound.
[0654] Yield: 209 mg, 98%; LC/MS t.sub.r 1.52 min; MS(ES+) m/z 380,
382 (M+H).
(ii) {3-[(5-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00145##
[0656] [3-(3-Bromo-5-fluoro-benzoylamino)-phenyl]-acetic acid ethyl
ester (209 mg, 0.55 mmol) was coupled to phenylboronic acid using
Method E, except that the reaction mixture was heated at 80.degree.
C. The crude residue was purified by column chromatography using
20% EtOAc in heptane to give the title compound.
[0657] Yield: 104 mg, 50%; LC/MS t.sub.r 1.66 min; MS(ES+) m/z 378
(M+H).
(iii) {3-[(5-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic acid
(52)
##STR00146##
[0659] The ethyl ester (104 mg, 0.28 mmol) was hydrolysed using
Method H to give the title compound.
[0660] Yield: 91 mg, 95%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 350
(M+H); HPLC Purity: 94%; .sup.1H NMR (250 MHz, MeOD) .delta. 3.60
(s, 2H), 7.14 (d, 1H), 7.30-7.36 (m, 5H), 7.60 (s, 1H), 7.65-7.72
(m, 3H) 7.80-7.86 (m, 1H) 7.97-8.00 (m, 1H).
(l) {3-[(2-Phenyl-1H-imidazole-5-carbonyl)-amino]-phenyl}-acetic
acid (53)
(i) {3-[(2-phenyl-1H-imidazole-5-carbonyl)-amino]-phenyl}acetic
acid ethyl ester
##STR00147##
[0662] 2-Phenyl-1H-imidazole-5-carboxylic acid (105 mg, 0.56 mmol)
was coupled with ethyl ester (6) (100 mg, 0.56 mmol) following
Method C to give the title compound.
[0663] Yield: 116 mg, 59%; LC/MS t.sub.r 1.19 min; MS(ES+) m/z 350
(M+H).
(ii) {3-[(2-Phenyl-1H-imidazole-5-carbonyl)-amino]-phenyl}-acetic
acid (53)
##STR00148##
[0665] The ethyl ester (50 mg, 0.14 mmol) was hydrolysed using
Method H to give the title compound.
[0666] Yield: 29 mg, 63%; LC/MS t.sub.r 1.39 min; MS(ES+) m/z 322
(M+H); HPLC Purity: 89%; .sup.1H NMR (250 MHz, MeOD) .delta. 3.66
(s, 2H), 7.10 (d, 1H), 7.31-7.37 (m, 1H), 7.43-7.56 (m, 3H),
7.67-7.68 (m, 2H), 7.87 (s, 1H), 7.97-8.00 (m, 2H).
(m) {3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acetic acid
(54)
(i) 2-Amino-thiazole-4-carboxylic acid ethyl ester hydrobromide
salt
##STR00149##
[0668] Thiourea (1.5 g, 20 mmol) and ethyl bromopyruvate (2.8 ml,
22 mmol) were heated at 100.degree. C. for 1 h. The reaction was
cooled and acetone (10 ml) was added. The mixture was then filtered
to give a yellow/brown solid and the crude material was
crystallised from hot ethanol (20 ml) to give the title compound as
the HBr salt (2.63 g). The liquor was concentrated and
recrystallised from hot EtOH (5 ml) to give further product (0.63
g).
[0669] Yield: 3.26 g, 64%; LC/MS t.sub.r 0.67 min; MS(ES+) m/z 173
(M+H); .sup.1H NMR (400 MHz, MeOD) .delta. 1.42 (t, 3H), 4.43 (q,
2H), 7.74 (s, 1H).
(ii) 2-Chloro-thiazole-4-carboxylic acid ethyl ester
##STR00150##
[0671] 2-Amino-thiazole-4-carboxylic acid ethyl ester hydrobromide
salt (506 mg, 2 mmol) was converted to the free base by
partitioning between aqueous saturated K.sub.2CO.sub.3 solution and
EtOAc. The organic layer was washed with brine, dried
(Na.sub.2SO.sub.4), filtered and the solvent removed in vacuo to
give the free base (306 mg, 89%).
[0672] The free based 2-amino-thiazole-4-carboxylic acid ethyl
ester (306 mg, 1.78 mmol) and CuCl (238 mg, 2.4 mmol) were
suspended in conc. HCl (8 ml) and the mixture cooled on a salt/ice
bath. A pre-cooled solution of NaNO.sub.2 (166 mg, 2.4 mmol) in
water (2 ml) was added over a period of 10 min. The mixture was
allowed to warm to room temperature over 1 h and was stirred for a
further 1 h. Water was added and the aqueous layer extracted with
EtOAc (3.times.10 ml). The combined EtOAc layers were washed with
brine, dried (Na.sub.2SO.sub.4), filtered and the solvent removed
in vacuo to give the title compound.
[0673] Yield: 251 mg, 74%; LC/MS t.sub.r 1.06 min; MS(ES+) m/z 192,
194 (M+H); .sup.1H NMR (250 MHz, CDCl.sub.3) .delta. 1.41 (t, 3H),
4.43 (q, 2H), 8.08 (s, 1H).
(iii) 2-Chloro-thiazole-4-carboxylic acid (79)
##STR00151##
[0675] The ethyl ester (120 mg, 0.63 mmol) was hydrolysed using
Method H to give the title compound.
[0676] Yield: 75 mg, 73%; LC/MS t.sub.r 0.77 min; MS(ES+) m/z 164,
166 (M+H).
(iv) {3-[(2-Chloro-thiazole-4-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00152##
[0678] 2-Chloro-thiazole-4-carboxylic acid (79) (70 mg, 0.43 mmol)
was coupled with ethyl ester (6) (77 mg, 0.43 mmol) following
Method C to give the title compound.
[0679] Yield: 114 mg, 82%; LC/MS t.sub.r 1.44 min; MS(ES+) m/z 325,
327 (M+H).
(v) {3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acetic acid
ethyl ester
##STR00153##
[0681] {3-[(2-Chloro-thiazole-4-carbonyl)-amino]-phenyl}-acetic
acid ethyl ester (114 mg, 0.35 mmol) was coupled to phenylboronic
acid using Method E, except that the reaction mixture was heated
for 140 min. The crude residue was purified by column
chromatography using 33% EtOAc in heptane to give the title
compound.
[0682] Yield: 37 mg, 29%; LC/MS t.sub.r 1.64 min; MS(ES+) m/z 367
(M+H).
(vi) {3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acetic acid
(54)
##STR00154##
[0684] The ethyl ester (37 mg, 0.10 mmol) was hydrolysed using
Method H to give the title compound.
[0685] Yield: 23 mg, 67%; LC/MS t.sub.r 1.62 min; MS(ES+) m/z 339
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, MeOD) .delta. 3.68
(s, 2H), 7.15 (d, 1H), 7.36-7.40 (m, 1H), 7.54-7.58 (m, 3H),
7.74-7.75 (m, 2H), 8.15-8.16 (m, 2H), 8.35 (s, 1H).
(n) 3-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic acid
(57)
(i) 5-Bromo-furan-2-carboxylic acid methyl ester (55)
##STR00155##
[0687] 5-Bromo-furan-2-carboxylic acid (2 g, 10.5 mmol) was
esterified with MeOH using Method B to give the title compound.
[0688] Yield: 1.54 g, 72%; LC-MS t.sub.r 1.24 min; MS(ES+) m/z 205,
207 (M+H).
(ii) 5-Phenyl-furan-2-carboxylic acid (56)
##STR00156##
[0690] 5-Bromo-furan-2-carboxylic acid methyl ester (5) (205 mg, 1
mmol) was coupled to phenylboronic acid (146 mg, 1.2 mmol) using
Method E except that once the reaction was complete, the solvents
were removed in vacuo. The crude residue was re-dissolved in EtOAc
(10 ml) and 1M NaOH (20 ml) was added. The aqueous layer was
extracted with EtOAc (3.times.10 ml), and the organic layer was
discarded. The aqueous layer was acidified to pH 1 with conc. HCl,
and extracted with EtOAc (3.times.10 ml). The combined organic
layers were dried (MgSO.sub.4), filtered, and the solvent removed
in vacuo to give the title compound.
[0691] Yield: 190 mg, 100%; LC-MS t.sub.r1.23 min; MS(ES+) m/z 189
(M+H).
(iii) 3-[9H-Fluoren-9-ylmethoxycarbonylamino)-methyl]-benzoic acid
methyl ester
##STR00157##
[0693] 3-[(9H-Fluoren-9-ylmethoxycarbonylamino)-methyl]-benzoic
acid (200 mg, 0.54 mmol) was esterified with MeOH using Method B to
give the title compound.
[0694] Yield: 193 mg, 93%; LC-MS t.sub.r1.64 min; MS(ES+) m/z 388
(M+H).
(iv) 3-Aminomethyl-benzoic acid methyl ester
##STR00158##
[0696] A 20% solution of piperidine in DMF (5 ml) was added to
3-[(9H-Fluoren-9-ylmethoxycarbonylamino)-methyl]-benzoic acid
methyl ester (193 mg, 0.5 mmol) and the reaction was stirred at
room temperature for 30 min. Water (10 ml) was added to the crude
reaction mixture, followed by 1M HCl (10 ml). The aqueous layer was
washed with EtOAc (3.times.10 ml) then basified to pH 9 with
saturated NaHCO.sub.3. The basic layer was extracted with EtOAc
(3.times.10 ml) and the aqueous layer was evaporated down to a
small volume, then further extracted with EtOAc (5.times.10 ml).
The combined organic layers were dried (MgSO.sub.4), filtered and
the solvent evaporated in vacuo to give the title compound.
[0697] Yield: 17 mg, 21%; LC-MS t.sub.r0.77 min; MS(ES+) m/z 166
(M+H).
(v) 3-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic acid
methyl ester
##STR00159##
[0699] 5-Phenyl-furan-2-carboxylic acid (6) (17 mg, 0.10 mmol) was
coupled to 3-aminomethyl-benzoic acid methyl ester (19.4 mg, 0.10
mmol) using Method D to give the title compound
[0700] Yield: 18 mg, 52%; LC-MS t.sub.r1.90 min; MS(ES+) m/z 336
(M+H).
(vi) 3-{[(5-Phenyl-furan-2-carbonyl)-amino]-methyl}-benzoic acid
(57)
##STR00160##
[0702] The ester (10 mg, 0.03 mmol) was dissolved in THF (0.1 ml)
and NaOH (20 mg, 0.5 mmol) was dissolved in H.sub.2O (0.1 ml). The
solutions were combined and stirred at room temperature for 6 h.
Further NaOH (50 mg, 1.25 mmol) was added and the reaction was
stirred overnight. The THF was removed under a stream of N.sub.2
and the aqueous layer was acidified to pH 3 with 2M HCl before
extracting with EtOAc (3.times.1 ml). The combined organic layers
were dried (MgSO.sub.4), filtered and the solvent removed in vacuo
to give the title compound as a white solid.
[0703] Yield: 5 mg, 52%; LC-MS t.sub.r1.76 min; MS(ES+) m/z 322
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD) .delta. 4.53
(s, 2H), 6.82 (d, 1H), 7.12 (d, 1H), 7.24 (t, 1H), 7.30-7.37 (m,
3H), 7.51 (d, 1H), 7.76 (d, 2H), 7.82 (d, 1H), 7.95 (s, 1H).
(o) 5-[(5-Phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic
acid (59)
(i) 5-Amino-1H-indole-2-carboxylic acid ethyl ester (58)
##STR00161##
[0705] 5-Nitro-1H-indole-2-carboxylic acid ethyl ester (500 mg, 2.1
mmol) was reduced using Method I to give the title compound.
[0706] Yield: 433 mg, 100%; LC-MS t.sub.r 0.84 min; MS(ES+) m/z 205
(M+H).
(ii) 5-[(5-Phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic
acid ethyl ester
##STR00162##
[0708] 5-Phenyl-furan-2-carboxylic acid (56) (35 mg, 0.19 mmol) was
coupled to 5-amino-1H-indole-2-carboxylic acid ethyl ester (42 mg,
0.20 mmol) using Method D to give the title compound.
[0709] Yield: 10 mg, 14%; LC-MS t.sub.r1.55 min; MS(ES+) m/z 375
(M+H).
(iii) 5-[(5-Phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic
acid (59)
##STR00163##
[0711] The ester (10 mg, 0.027 mmol) was dissolved in THF (0.5 ml)
and water (2 ml). LiOH.H.sub.2O (11 mg, 0.27 mmol) was then added
as a solid. The resulting solution was stirred for 48 h at room
temperature and then heated to 40.degree. C. for 3 h with a few
drops of MeOH. The THF was removed in vacuo and the basic solution
was extracted with EtOAc (3.times.1 ml). The aqueous layer was
acidified to pH 1 with conc. HCl and then extracted with EtOAc
(3.times.1 ml). The combined organic layers were evaporated in
vacuo to give the title compound.
[0712] Yield: 5.4 mg, 58%; LC/MS t.sub.r 1.34 min; MS(ES+) m/z 347
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD) .delta.
6.83-6.89 (m, 1H), 7.03-7.07 (m, 1H), 7.20-7.29 (m, 2H), 7.30-7.38
(m, 3H), 7.40-7.45 (m, 1H), 7.78-7.85 (m, 2H), 7.90 (s, 1H).
(p) 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acrylic acid
(61)
(i) 3-(3-Amino-phenyl)-acrylic acid ethyl ester (60)
##STR00164##
[0714] 3-(3-Nitro-phenyl)-acrylic acid ethyl ester (500 mg, 2.3
mmol) was reduced using Method J to give the title compound.
[0715] Yield: 430 mg, 100%; LC-MS t.sub.r0.92 min; MS(ES+) m/z 192
(M+H).
(ii) 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acrylic acid
ethyl ester
##STR00165##
[0717] 5-Phenyl-furan-2-carboxylic acid (56) (35 mg, 0.19 mmol) was
coupled to 3-(3-amino-phenyl)-acrylic acid ethyl ester (60) (39 mg,
0.20 mmol) using Method D to give the title compound.
[0718] Yield: 13 mg, 18%; LC-MS t.sub.r1.65 min; MS(ES+) m/z 362
(M+H).
(iii) 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-acrylic acid
(61)
##STR00166##
[0720] The ester (13 mg, 0.036 mmol) was dissolved in THF (0.5 ml)
and water (2 ml). LiOH.H.sub.2O (15 mg, 0.36 mmol) was then added
as a solid and the resulting solution was stirred at room
temperature for 18 h. The THF was removed in vacuo and the basic
solution was extracted with EtOAc (3.times.1 ml). The aqueous layer
was acidified to pH 1 with conc. HCl and then extracted with EtOAc
(3.times.1 ml). The combined organic layers were evaporated in
vacuo to give the title compound.
[0721] Yield: 3.4 mg, 28%; LC/MS t.sub.r 1.34 min; MS(ES+) m/z 334
(M+H); HPLC Purity: 94%; .sup.1H NMR (400 MHz; MeOD) .delta. 6.43
(d, 1H), 6.92 (d, 1H), 7.25-7.41 (m, 6H), 7.59 (d, 1H), 7.72 (d,
1H), 7.86 (m, 2H), 7.91 (s, 1H).
(q) 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic acid
(62)
(i) 3-(3-Amino-phenyl)-propionic acid methyl ester
##STR00167##
[0723] 3-(3-Amino-phenyl)-propionic acid (495 mg, 3 mmol) was
esterified with MeOH using Method A, except that the residue was
partitioned between EtOAc (10 ml) and saturated aqueous NaHCO.sub.3
(10 ml). The organic layer was dried (MgSO.sub.4), filtered and
evaporated in vacuo to give the title compound.
[0724] Yield: 448 mg, 83%; LC-MS t.sub.r 0.78 min; MS(ES+) m/z 180
(M+H).
(ii) 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic
acid methyl ester
##STR00168##
[0726] 5-Phenyl-furan-2-carboxylic acid (56) (40 mg, 0.21 mmol) was
coupled to 3-(3-amino-phenyl)-propionic acid methyl ester (41 mg,
0.23 mmol) using Method D to give the title compound.
[0727] Yield: 38 mg, 52%; LC-MS t.sub.r1.51 min; MS(ES+) m/z 350
(M+H).
(iii) 3-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenyl}-propionic
acid (62)
##STR00169##
[0729] The ester (38 mg, 0.11 mmol) was dissolved in THF (1.5 ml)
and NaOH (76 mg, 1.9 mmol) was dissolved in H.sub.2O (1 ml). The
solutions were combined and stirred at room temperature for 1 h.
The THF was removed in vacuo and the aqueous layer was extracted
with EtOAc (3.times.1 ml). The aqueous layer was then acidified to
pH 1 with 1M HCl and then extracted with EtOAc (3.times.1 ml). The
combined organic layers were dried (MgSO.sub.4), filtered, and the
solvent removed in vacuo to give the title compound.
[0730] Yield: 31 mg, 86%; LC/MS t.sub.r 1.39 min; MS(ES+) m/z 336
(M+H); HPLC Purity: 93%; .sup.1H NMR (250 MHz; CDCl.sub.3) .delta.
2.71 (t, 2H), 3.01 (t, 2H), 6.81 (d, 1H), 7.01 (d, 1H), 7.22-7.58
(m, 7H), 7.74 (d, 2H), 8.08 (s, 1H).
(r) 6-[(5-Phenyl-furan-2-carbonyl)-amino]-naphthalene-2-carboxylic
acid (63)
(i) 6-Amino-naphthalene-2-carboxylic acid methyl ester
##STR00170##
[0732] 6-Amino-naphthalene-2-carboxylic acid (561 mg, 3 mmol) was
esterified with MeOH using Method B to give the title compound.
[0733] Yield: 360 mg, 59%; MS(ES+) m/z 203 (M+H).
(ii) 6-[(5-Phenyl-furan-2-carbonyl)-amino]-naphthalene-2-carboxylic
acid methyl ester
##STR00171##
[0735] 5-Phenyl-furan-2-carboxylic acid (56) (50 mg, 0.26 mmol) was
coupled to 6-amino-naphthalene-2-carboxylic acid methyl ester (53
mg, (0.26 mmol) using Method C to give the title compound.
[0736] Yield: 17 mg, 17%; MS(ES+) m/z 372 (M+H).
(iii)
6-[(5-Phenyl-furan-2-carbonyl)-amino]-naphthalene-2-carboxylic acid
(63)
##STR00172##
[0738] The ester (17 mg, 0.046 mmol) was dissolved in THF (1.5 ml)
and MeOH (2 ml). NaOH (34 mg, 0.85 mmol) was dissolved in H.sub.2O
(1 ml). The solutions were combined and stirred at room temperature
for 3.5 h. Further NaOH (34 mg, 0.85 mmol) was then added and the
reaction mixture was stirred for 18 h at room temperature. The THF
was removed under a stream of N.sub.2, then MeOH (2 ml) was added
and the resulting solution was heated at 40.degree. C. for 2 h. The
reaction was cooled to room temperature and stirred for 18 h. The
MeOH was removed under a stream of N.sub.2 and the aqueous layer
extracted with EtOAc (3.times.1 ml). The aqueous layer was then
acidified to pH 1 with 1M HCl and extracted with EtOAc (3.times.1
ml). The combined organic layers were dried (MgSO.sub.4), filtered,
and the solvents removed in vacuo to give the title compound.
[0739] Yield: 15 mg, 86%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 378
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz; d-DMSO) .delta.
7.22 (s, 1H), 7.40-7.48 (m, 1H), 7.50-7.57 (m, 3H), 7.92-8.02 (m,
5H), 8.13 (d, 1H), 8.55 (d, 2H), 10.52 (s, 1H), 13.01 (s, 1H).
(s)
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (66)
(i) (3-Acetylamino-phenoxy)-acetic acid ethyl ester
##STR00173##
[0741] To a solution of N-(3-hydroxy-phenyl)-acetamide (0.5 g, 3.3
mmol) in acetone (5 ml) was added K.sub.2CO.sub.3 (0.46 g, 3.3
mmol), ethyl bromoacetate (0.67 g, 4.0 mmol) and 10 4 A molecular
sieves. The reaction mixture was then heated in the microwave for 1
h at 100.degree. C. (150 W, 200 psi). The reaction mixture was
filtered and the acetone layer evaporated in vacuo. This residue
was dissolved in EtOAc (10 ml) and washed with 2M KOH (5
ml.times.2). The organic layer was dried (Na.sub.2SO.sub.4),
filtered and the solvent removed in vacuo to give the title
compound as a colourless oil which solidified upon standing.
[0742] Yield: 700 mg, 89%; LC/MS t.sub.r 1.04 min; MS(ES+) m/z 238
(M+H).
(ii) (3-Amino-phenoxy)-acetic acid
##STR00174##
[0744] The ester (0.25 g, 1 mmol) was suspended in 1.2 M HCl and
heated to 100.degree. C. for 80 min. The water was removed in vacuo
to give the title compound as the hydrochloride salt.
[0745] Yield: 170 mg, 83%; LC/MS t.sub.r 0.17 and 0.56 min; MS(ES+)
m/z 168 (M+H).
(iii) (3-Amino-phenoxy)-acetic acid ethyl ester (64)
##STR00175##
[0747] The carboxylic acid (100 mg, 0.6 mmol) was suspended in EtOH
(1 ml) at 0.degree. C. and SOCl.sub.2 (78 mg, 0.7 mmol) was added
dropwise. The reaction mixture was allowed to warm to room
temperature and stirred for 18 h. The solvent was removed in vacuo
to give the title compound as the hydrochloride salt.
[0748] Yield: 139 mg, 100%; LC/MS t.sub.r 0.79 min; MS(ES+) m/z 196
(M+H); .sup.1H NMR (400 MHz; CDCl.sub.3) .delta. 1.26 (t, 3H), 4.23
(q, 2H), 4.58 (s, 2H), 6.86 (d, 1H), 7.15 (s, 2H), 7.25 (t,
1H).
(iv) 5-(3-Chloro-phenyl)-furan-2-carboxylic acid (65)
##STR00176##
[0750] 5-Bromo-2-furoic acid (1 g, 5.8 mmol) was coupled to
3-chloro-phenylboronic acid (683 g, 4.4 mmol) acid using Method F
to give the title compound.
[0751] Yield: 510 mg, 52%; LC/MS t.sub.r 1.24 min; MS(ES+) m/z 223,
225 (M+H).
(v)
(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00177##
[0753] Carboxylic acid (65) (67 mg, 0.3 mmol) was coupled to ethyl
ester (64) (58 mg, 0.25 mmol) using Method C. The crude residue was
purified by column chromatography eluting with a stepped gradient
of 10-20% EtOAc in heptane to give the title compound.
[0754] Yield: 75 mg, 75%; LC/MS t.sub.r 1.65 min; MS(ES+) m/z 400,
402 (M+H).
(vi)
(3-{[5-(3-Chloro-Thenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (66)
##STR00178##
[0756] The ester (64 mg, 0.16 mmol) was dissolved in MeOH (1.5 ml),
and a solution of NaOH (128 mg, 3.2 mmol) in water (0.5 ml) was
added. The reaction mixture was stirred for 1 h at room temperature
before the MeOH was removed in vacuo. The aqueous layer was washed
with EtOAc (2.times.2 ml) and then acidified with 2M HCl until a
white precipitate formed. This was then extracted with EtOAc (2
ml). The organic layer was dried (Na.sub.2SO.sub.4), filtered and
the solvent removed in vacuo to give the title compound.
[0757] Yield: 30 mg, 50%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 372,
374 (M+H); HPLC Purity: 99%; .sup.1H NMR (400 MHz; DMSO) .delta.
4.24 (s, 2H), 6.69 (d, 1H), 7.31 (t, 1H), 7.42 (m, 3H), 7.55 (m,
2H), 7.64 (t, 1H), 8.05 (d, 1H), 8.21 (s, 1H), 10.38 (s, 1H).
(t)
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (68)
(i) 5-(3,5-Dichloro-phenyl)-furan-2-carboxylic acid (67)
##STR00179##
[0759] 5-Bromo-2-furoic acid (1 g, 4.8 mmol) was coupled to
3,5-dichloro-phenylboronic acid (833 g, 4.4 mmol) acid using Method
F to give the title compound.
[0760] Yield: 500 mg, 44%; LC/MS t.sub.r 1.48 min; MS(ES+) m/z 257,
259 (M+H).
(ii)
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00180##
[0762] Carboxylic acid (67) (77 mg, 0.3 mmol) was coupled to ethyl
ester (9) (58 mg, 0.25 mmol) using Method C. The crude residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[0763] Yield: 109 mg, 100%; LC/MS t.sub.r 1.78 min; MS(ES+) m/z
434, 436 (M+H).
(iii)
(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-aceti-
c acid (68)
##STR00181##
[0765] The ester (70 mg, 0.16 mmol) was dissolved in MeOH (1.5 ml)
and a solution of NaOH (140 mg, 3.5 mmol) in water (0.5 ml) was
added. The reaction mixture was stirred for 1 h at room temperature
and the MeOH was removed in vacuo. The aqueous layer was washed
with EtOAc (2.times.2 ml) and then acidified with 2M HCl until a
white precipitate formed. This was then extracted with EtOAc (2
ml). The organic layer was dried (Na.sub.2SO.sub.4), filtered and
the solvent removed in vacuo to give the title compound.
[0766] Yield: 40 mg, 61%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 406,
408 (M+H); HPLC Purity: 99%; .sup.1H NMR (400 MHz; DMSO) .delta.
4.20 (s, 2H), 6.65 (d, 1H), 7.25 (t, 1H), 7.35 (s, 2H), 7.47 (d,
2H), 7.69 (s, 1H), 8.15 (s, 2H).
(u)
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (69)
(i)
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00182##
[0768] Carboxylic acid (65) (58 mg, 0.26 mmol) was coupled to ethyl
ester (60) (50 mg, 0.26 mmol) using Method C. The crude residue was
purified by column chromatography eluting with a stepped gradient
of 10-15% EtOAc in heptane to give the title compound.
[0769] Yield: 67 mg, 65%; LC/MS t.sub.r 1.72 min; MS(ES+) m/z 396,
398 (M+H).
(ii)
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (69)
##STR00183##
[0771] The ester (67 mg, 0.17 mmol) was dissolved in THF (1 ml) and
water (0.25 ml). To this was added LiOH.H.sub.2O (20 mg, 0.48 mmol)
and the reaction was stirred for 2 h at room temperature. The THF
was removed in vacuo and the aqueous layer was washed twice with
EtOAc (2.times.2 ml) then acidified with 2M HCl until a white
precipitate formed. This was then extracted with EtOAc (2 ml). The
organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo to give the title compound.
[0772] Yield: 23 mg, 37%; LC/MS t.sub.r 1.51 min; MS(ES+) m/z 367,
369 (M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz; DMSO) .delta.
6.41 (d, 1H), 7.24 (d, 1H), 7.36 (m, 4H), 7.45 (t, 1H), 7.51 (d,
1H), 7.74 (m, 1H), 7.87 (m, 1H), 7.92 (s, 1H), 8.04 (t, 1H), 10.25
(s, 1H).
(v)
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acryli-
c acid (70)
(i)
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acryli-
c acid ethyl ester
##STR00184##
[0774] Carboxylic acid (67) (67 mg, 0.26 mmol) was coupled to ethyl
ester (60) (50 mg, 0.26 mmol) using Method C. The crude residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[0775] Yield: 90 mg, 80%; LC/MS t.sub.r 1.84 min; MS(ES+) m/z 430,
432 (M+H).
(ii)
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acryl-
ic acid (70)
##STR00185##
[0777] The ester (90 mg, 0.21 mmol) was dissolved in THF (1 ml) and
water (0.25 ml). To this was added LiOH.H.sub.2O (30 mg, 0.71 mmol)
and the resulting solution was stirred for 2 h at room temperature.
The THF was removed in vacuo and the aqueous layer was washed twice
with EtOAc (2.times.2 ml) then acidified with 2M HCl until a white
precipitate formed. This was then extracted with EtOAc (2 ml). The
organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo to give the title compound.
[0778] Yield: 41 mg, 48%; LC/MS t.sub.r 1.63 min; MS(ES+) m/z 402,
404 (M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz; DMSO) .delta.
6.42 (d, 1H), 7.37 (m, 4H), 7.51 (d, 1H), 7.55 (t, 1H), 7.73 (d,
1H), 7.91 (s, 1H), 8.04 (d, 2H), 10.29 (s, 1H).
(x)
3-(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (71)
(i) 5-(4-Fluoro-phenyl)-furan-2-carboxylic acid
##STR00186##
[0780] 4-Fluoro-phenylboronic acid (611 mg, 4.4 mmol) was coupled
to 5-bromo-2-furoic acid (1 g, 4.8 mmol) using Method F to give the
title compound.
[0781] Yield: 350 mg, 39%; LC/MS t.sub.r 1.24 min; MS(ES+) m/z 207
(M+H).
(ii)
3-(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00187##
[0783] 5-(4-Fluoro-phenyl)-furan-2-carboxylic acid (54 mg, 0.26
mmol) was coupled to ethyl ester (60) (50 mg, 0.26 mmol) using
Method C. The crude residue was purified by column chromatography
eluting with 10% EtOAc in heptane to give the title compound.
[0784] Yield: 98 mg, 100%; LC/MS t.sub.r 1.67 min; MS(ES+) m/z 380
(M+H).
(iii)
3-(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (71)
##STR00188##
[0786] The ester (109 mg, 0.29 mmol) was dissolved in THF (0.4 ml)
and water (0.1 ml). To this was added LiOH.H.sub.2O (126 mg, 3.1
mmol) and the resulting solution was stirred for 2 h at room
temperature. The THF was removed in vacuo and the aqueous layer was
washed twice with EtOAc (2.times.2 ml) then acidified with 2M HCl
until a white precipitate formed. This was then extracted with
EtOAc (2 ml). The combined organic layers were dried
(Na.sub.2SO.sub.4), filtered and the solvent removed in vacuo to
give the title compound.
[0787] Yield: 48 mg, 47%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 352
(M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz; DMSO) .delta. 6.47
(d, 1H), 7.18 (d, 1H), 7.23 (d, 1H), 7.29 (d, 1H), 7.41 (q, 3H),
7.54 (d, 1H), 7.80 (d, 1H), 7.93 (s, 1H), 8.11 (q, 2H), 10.42 (s,
1H).
(y)
5-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-1H-indole-2-carboxyli-
c acid (72)
(i)
5-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-1H-indole-2-carboxyli-
c acid ethyl ester
##STR00189##
[0789] 5-(3-Chloro-phenyl)-furan-2-carboxylic acid (65) (54 mg,
0.24 mmol) was coupled to ethyl ester (58) (50 mg, 0.24 mmol) using
Method C. The crude residue was purified by column chromatography
eluting with 20% EtOAc in heptane to give the title compound.
[0790] Yield: 42 mg, 43%; LC/MS t.sub.r 1.64 min; MS(ES+) m/z 409,
411 (M+H); HPLC Purity: 92%.
(ii)
5-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-1H-indole-2-carboxyl-
ic acid (72)
##STR00190##
[0792] The ester (42 mg, 0.10 mmol) was dissolved in THF (0.2 ml)
and water (0.05 ml). To this was added LiOH.H.sub.2O (42 mg, 1
mmol) and the resulting solution was stirred for 2 h at room
temperature then at 35.degree. C. for 2 h. The THF was removed
under a stream of N.sub.2 and the aqueous layer acidified with 2M
HCl until a white precipitate formed. This was then extracted with
EtOAc (2 ml). The organic layer was dried (Na.sub.2SO.sub.4),
filtered, and the solvent removed in vacuo to give the title
compound which was re-suspended in hot DCM (1.5 ml), then hot MeCN
(1.5 ml), filtered, and dried in vacuo.
[0793] Yield: 30 mg, 79%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 380,
382 (M+H); HPLC Purity: 97%; .sup.1H NMR (360 MHz; DMSO): .delta.
6.55 (s, 1H), 7.22-7.42 (m, 6H), 7.48 (t, 1H), 7.80 (s, 1H), 7.91
(d, 1H), 8.10 (s, 1H), 10.08 (s, 1H), 11.07 (s, 1H).
Example 8
(a) 5-Phenyl-furan-2-carboxylic acid
(3-carbamoylmethyl-phenyl)-amide (73)
##STR00191##
[0795] The carboxylic acid (10) (50 mg, 0.15 mmol) was coupled to
NH.sub.4OH (0.01 ml, 0.15 mmol) using Method C. The crude compound
was purified by column chromatography, eluting with a stepped
gradient of 80-100% EtOAc in heptane to give the title
compound.
[0796] Yield: 15 mg, 31%; LC/MS t.sub.r 1.23 min; MS(ES+) m/z 321
(M+H); HPLC Purity: 95%; .sup.1H NMR (400 MHz; CDCl.sub.3) .delta.
3.44 (m, 2H), 6.98 (brs, 2H), 7.08 (d, 1H), 7.24 (d, 1H), 7.35 (t,
1H), 7.46 (t, 2H), 7.56 (t, 2H), 7.70 (s, 1H), 7.74 (d, 1H), 8.04
(d, 2H), 10.23 (s, 1H).
(b) Phenyl-furan-2-carboxylic acid
[3-(2-hydroxy-ethyl)-phenyl]-amide (74)
##STR00192##
[0798] The carboxylic acid (10) (50 mg, 0.15 mmol) was dissolved in
anhydrous THF (0.1 ml) and placed under an atmosphere of N.sub.2.
The solution was cooled to -78.degree. C. using acetone/dry ice and
stirred for 10 min. LiAlH.sub.4 (1M in THF) was added dropwise
(0.31 ml, 0.31 mmol) and the resulting solution was stirred for 10
min at -78.degree. C., then allowed to warm to room temperature and
stirred for a further 2 h. After cooling to 5.degree. C. using
ice/water, the reaction mixture was quenched by dropwise addition
of water (1 ml) then neutralised to pH 7 with 1M NaOH and extracted
with EtOAc (2.times.1 ml). The combined organic layers were dried
(Na.sub.2SO.sub.4), filtered and the solvent removed in vacuo. The
crude residue was purified by column chromatography, eluting in 60%
EtOAc in heptane to give the title compound.
[0799] Yield: 34 mg, 70; LC/MS t.sub.r 1.35 min; MS(ES+) m/z 308
(M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz; CDCl.sub.3) .delta.
2.90 (t, 2H), 3.91 (t, 2H), 6.80 (d, 1H), 7.05 (d, 1H), 7.03 (d,
1H), 7.29-7.41 (m, 3H), 7.46 (t, 2H), 7.58 (d, 2H), 7.76 (d, 2H),
8.09 (s, 1H).
(c) 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (75)
(i) (3-Amino-phenyl)-acetonitrile (80)
##STR00193##
[0801] A solution of 3-nitrophenyl acetonitrile (500 mg, 3.1 mmol)
in 5% AcOH (10 ml) was heated to 80.degree. C. Iron powder (1.5 g,
27 mmol) was then added and the resulting mixture stirred for 2 h.
The reaction mixture was filtered through celite and the filter
cake washed with MeCN (4.times.50 ml). The combined MeCN layers
were evaporated in vacuo and the residue was re-dissolved in EtOAc
(30 ml) followed by 2M HCl (30 ml). The aqueous layer was
separated, basified to pH 10 with 6M NaOH, and extracted with EtOAc
(3.times.80 ml). The combined organic layers were dried
(MgSO.sub.4), filtered and the solvent removed in vacuo to give the
title compound.
[0802] Yield: 140 mg, 34%; .sup.1H NMR (400 MHz, CDCl.sub.3):
.delta. 3.65 (s, 2H), 3.75 (s, 2H), 6.60-6.70 (m, 3H), 7.15 (t,
1H).
(ii) 5-Phenyl-furan-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00194##
[0804] 5-Phenyl-2-furoic acid (56) (223 mg, 1.2 mmol) was coupled
to 3-aminophenyl acetonitrile (80) (157 mg, 1.19 mmol), using
Method C. The crude residue was purified by column chromatography,
eluting in 17% EtOAc in heptane to give the title compound.
[0805] Yield: 70 mg, 19%; LC/MS t.sub.r 1.47 min; MS(ES+) m/z 303
(M+H).
(iii) 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide
##STR00195##
[0807] To a solution of 5-phenyl-furan-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide (70 mg, 0.23 mmol) in toluene (3 ml)
was added Me.sub.3SnN.sub.3 (56 mg, 0.28 mmol). After heating to
reflux for 18 h, additional Me.sub.3SnN.sub.3 (56 mg, 0.28 mmol)
and toluene (2 ml) were added and the reaction was heated to reflux
for a further 18 h. After this time, 2M NaOH (2 ml) and hexane (2
ml) were added to the reaction mixture and stirred for 10 min.
Water (1 ml) was added and the organic layer separated. EtOAc (2
ml) was added to the aqueous layer and the solution stirred for 2
min before the organic layer was separated. The combined organic
layers were discarded. The aqueous layer was then acidified to pH 5
with 2M HCl then EtOAc (2.5 ml) was added and the solution stirred
for 10 min after which time the organic layer was separated. EtOAc
(2.5 ml) was added to the aqueous layer and the solution stirred
for 1 hour. The EtOAc layer was separated and these combined
organic layers were evaporated in vacuo to give the title
compound.
[0808] Yield: 16 mg, 20%; LC/MS t.sub.r 1.31 min; MS(ES+) m/z 346
(M+H); HPLC Purity: 98%; NMR (400 MHz, DMSO): .delta. 4.2 (s, 2H),
7.1 (d, 1H), 7.25 (s, 1H), 7.35 (t, 1H), 7.4-7.49 (m, 2H), 7.55 (t,
2H), 7.65 (s, 1H), 7.75 (d, 1H), 8.0 (d, 2H), 10.25 (s, 1H).
(d) 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-yl)-phenyl]-amide (177)
(i) 5-Phenyl-furan-2-carboxylic acid (3-cyano-phenyl)-amide
##STR00196##
[0810] Carboxylic acid (56) (150 mg, 0.80 mmol) was coupled to
3-amino-benzonitrile (94 mg, 0.80 mmol) using Method C. The residue
was purified by column chromatography eluting with 17% EtOAc in
heptane to give the title compound.
[0811] Yield: 80 mg, 35%; LC/MS t.sub.r 1.51 min; MS(ES+) m/z 289
(M+H).
(ii) 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-yl)-phenyl]-amide (177)
##STR00197##
[0813] The nitrile (80 mg, 0.28 mmol) was reacted with
Me.sub.3SnN.sub.3 using Method K. The solid was then re-dissolved
in EtOAc (2 ml) and 2M NaOH (2 ml). The layers were separated and
the aqueous layer was acidified to pH 5 with 2M HCl and extracted
with EtOAc (2 ml). The combined organic layers were evaporated in
vacuo and the residue triturated with TBME (2.times.2 ml). The
solid was dissolved in MeOH (1.5 ml) and washed with heptane
(2.times.2 ml). MeOH was removed in vacuo to give the title
compound. Yield: 15 mg, 16%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z
332 (M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz, DMSO): .delta.
7.07 (d, 1H), 7.19-7.42 (m, 5H), 7.60 (d, 1H), 7.69 (d, 1H), 7.89
(d, 2H), 8.18-8.20 (m, 1H), 10.13 (s, 1H).
(e) 5-(3-Chloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (81)
(i)
{3-[5-(3-Chloro-phenyl)-furan-2-carbonyl]-phenyl}-acetonitrile
##STR00198##
[0815] Carboxylic acid (65) (127 mg, 0.57 mmol) was coupled to
aniline (80) (75 mg, 0.57 mmol) using Method C. The crude residue
was purified by column chromatography eluting with 17% EtOAc in
heptane to give the title compound.
[0816] Yield: 65 mg, 34%; LC/MS t.sub.r 1.57 min; MS(ES+) m/z 337,
339 (M+H).
(ii) 5-(3-Chloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (81)
##STR00199##
[0818] The nitrile (65 mg, 0.19 mmol) was reacted with
Me.sub.3SnN.sub.3 using Method K. The solid was re-dissolved in
MeOH (2.5 ml) and washed with heptane (5.times.3 ml). The product
was further purified by column chromatography eluting with a
stepped gradient of 10-100% EtOAc in heptane to give the title
compound.
[0819] Yield: 1.2 mg, 2%; LC/MS t.sub.r 1.48 min; MS(ES+) m/z 380,
382 (M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz, DMSO): .delta.
4.38 (s, 2H), 7.11 (d, 1H), 7.35-7.57 (m, 3H), 7.49-7.53 (m, 1H),
7.56-7.62 (t, 1H), 7.69 (s, 1H), 7.79 (d, 1H), 8.00 (d, 1H), 8.19
(s, 1H), 10.32 (s, 1H).
(f) 5-(3,5-Dichloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (82)
(i) 5-(3,5-Dichloro-phenyl)-furan-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00200##
[0821] Carboxylic acid (67) (62 mg, 0.24 mmol) was coupled to
aniline (80) (32 mg, 0.24 mmol) using Method C. After work-up, the
solid was recrystallised from MeCN (3 ml) to give the title
compound.
[0822] Yield: 63 mg, 71%; LC/MS t.sub.r 1.73 min; MS(ES+) m/z 371,
373 (M+H).
(ii) 5-(3,5-Dichloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (82)
##STR00201##
[0824] The nitrile (63 mg, 0.17 mmol) was reacted with
Me.sub.3SnN.sub.3 using Method K. The residue was purified by
column chromatography, flushing with heptane (200 ml) and eluting
with 50% MeOH in EtOAc. The solid was then triturated with MeOH (3
ml) to give the title compound.
[0825] Yield: 4.2 mg, 6%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 414,
416 (M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz, DMSO): .delta.
4.48 (s, 2H), 7.21 (d, 1H), 7.43-7.60 (m, 3H), 7.75-7.81 (m, 2H),
7.88 (d, 1H), 8.26 (s, 2H), 10.45 (s, 1H).
(g) 5-(4-Fluoro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (85)
(i) 5-Bromo-furan-2-carboxylic acid (3-cyanomethyl-phenyl)-amide
(83)
##STR00202##
[0827] 5-Bromo-furan-2-carboxylic acid (1.68 g, 8.80 mmol) was
coupled to aniline (80) (1.16 g, 8.80 mmol), using Method C. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[0828] Yield: 399 mg, 15%; LC/MS t.sub.r 1.31 min; MS(ES+) m/z 305,
307 (M+H).
(ii) 5-Bromo-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (84)
##STR00203##
[0830] Nitrile (83) (162 mg, 0.53 mmol) was treated with
Me.sub.3SnN.sub.3 using Method K. The residue was purified by
column chromatography, flushing with heptane (200 ml) and eluting
with 50% EtOAc in heptane to give the title compound.
[0831] Yield: 35 mg, 19%; LC/MS t.sub.r 1.11 min; MS(ES+) m/z 348,
350 (M+H).
(iii) 5-(4-Fluoro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (85)
##STR00204##
[0833] The furyl bromide (84) (100 mg, 0.29 mmol) was coupled to
4-fluoro-phenylboronic acid (44 mg, 0.32 mmol) using Method E. The
solvents were removed in vacuo as described, but the residue was
dissolved in 2M NaOH (10 ml) and washed with EtOAc (2.times.10 ml).
The aqueous layer was acidified to pH 1 with 2M HCl until a white
precipitate formed and extracted with EtOAc (2.times.10 ml). The
organic layer was dried (MgSO.sub.4), filtered and the solvent
removed in vacuo to give the title compound. Yield: 13 mg, 12%;
LC/MS t.sub.r 1.32 min; MS(ES+) m/z 364 (M+H); HPLC Purity: 87%;
.sup.1H NMR (400 MHz, DMSO): .delta. 4.31 (s, 2H), 7.04 (d, 1H),
7.17 (d, 1H), 7.32-7.41 (m, 4H), 7.61 (s, 1H), 7.73 (d, 1H), 8.02
(t, 2H), 10.21 (s, 1H).
(h) 5-(3-Fluoro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (86)
(i) 5-(3-Fluoro-phenyl)-furan-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00205##
[0835] The furyl bromide (83) (135 mg, 0.44 mmol) was coupled to
3-fluoro-phenylboronic acid (68 mg, 0.49 mmol) using Method E. The
crude residue was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0836] Yield: 40 mg, 28%; LC/MS t.sub.r 1.47 min; MS(ES+) m/z 321
(M+H).
(ii) 5-(3-Fluoro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (86)
##STR00206##
[0838] The nitrile (40 mg, 0.13 mmol) was treated with TMSN.sub.2
and Bu.sub.2SnO using Method L. After a first treatment, TMSN.sub.2
(58 mg, 0.50 mmol) and Bu.sub.2SnO (6 mg, 0.025 mmol) were added,
and the mixture was heated in the microwave for a further 20 min.
After work-up, the residue was dissolved in MeOH (2 ml) and washed
with heptane (3.times.3 ml). The layers were separated and the MeOH
was removed in vacuo. The solid was then triturated with heptane
(4.times.2 ml) to give the title compound.
[0839] Yield: 16 mg, 34%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 364
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO): .delta. 4.24
(s, 2H), 7.02 (d, 1H), 7.18-7.34 (m, 3H), 7.37 (d, 1H), 7.52 (q,
1H), 7.59 (s, 1H), 7.69 (d, 1H), 7.81 (d, 1H), 7.89 (d, 1H), 10.21
(s, 1H).
(i) 5-(4-Chloro-phenyl)-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (87)
##STR00207##
[0841] The bromo-derivative (84) (100 mg, 0.29 mmol) was coupled to
4-chloro-phenylboronic acid (49 mg, 0.32 mmol) using Method E.
After reaction, the solvents were removed under a stream of
N.sub.2, and the residue was dissolved in saturated NaHCO.sub.2
solution (5 ml) and washed with EtOAc (5 ml). The aqueous layer was
acidified to pH 1 with 2M HCl until a white precipitate formed and
extracted with EtOAc (2.times.5 ml). The organic layer was dried
(MgSO.sub.4), filtered and the solvent removed in vacuo. The
residue was triturated with MeCN (4 ml) and further purified by
preparative HPLC to give the title compound.
[0842] Yield: 11 mg, 10%; LC/MS t.sub.r 1.52 min; MS(ES+) m/z 380,
382 (M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO): .delta.
4.20 (s, 2H), 6.92 (d, 1H), 7.12 (d, 1H), 7.20-7.29 (m, 2H),
7.42-7.50 (m, 3H), 7.60 (d, 1H), 7.89 (d, 2H), 10.11 (s, 1H).
(j) 5-Phenyl-furan-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]-phenyl}-amide (89)
(i) 3-(3-Amino-phenyl)-acrylonitrile (88)
##STR00208##
[0844] A solution of 3-(3-nitro-phenyl)-acrylonitrile (500 mg, 2.87
mmol) in 5% aqueous AcOH (10 ml) was heated to 80.degree. C. Iron
powder (1.44 g, 25.8 mmol) was then added and the resulting mixture
was stirred for 3 h. The reaction mixture was filtered through
celite and the filter cake washed with MeCN (4.times.50 ml). The
combined MeCN layers were evaporated in vacuo and the residue was
re-dissolved in EtOAc (30 ml) and HCl (30 ml). The aqueous layer
was separated, basified to pH 10 with 6M NaOH, and extracted with
EtOAc (3.times.80 ml). The combined organic layers were dried
(MgSO.sub.4), filtered and the solvent removed in vacuo to give the
title compound.
[0845] Yield: 297 mg, 71%; LC/MS t.sub.r 0.70 min; MS(ES+) m/z 186
(M+MeCN+H).
(ii) 5-Phenyl-furan-2-carboxylic acid
[3-(2-cyano-vinyl)-phenyl]-amide
##STR00209##
[0847] Carboxylic acid (56) (120 mg, 0.64 mmol) was coupled to
aniline (88) (92 mg, 0.64 mmol), using Method C to give the title
compound.
[0848] Yield: 113 mg, 56%; LC/MS t.sub.r 1.55 min; MS(ES+) m/z 315
(M+H).
(iii) 5-Phenyl-furan-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]-phenyl}-amide (89)
##STR00210##
[0850] The nitrile (113 mg, 0.36 mmol) was treated with
Me.sub.3SnN.sub.3 using Method K. After work-up, the residue was
purified by column chromatography, flushing with heptane (200 ml)
and eluting with 50% MeOH in EtOAc. Column chromatography was
repeated eluting with 100% EtOAc. The solid was further purified by
preparative HPLC to give the title compound. Yield: 4.7 mg, 4%;
LC/MS t.sub.r 1.40 min; MS(ES+) m/z 358 (M+H); HPLC Purity: 100%;
.sup.1H NMR (400 MHz, DMSO): .delta. 7.22 (d, 1H), 7.33 (d, 1H),
7.41-7.58 (m, 6H), 7.69 (d, 1H), 7.83 (d, 1H), 8.02 (d, 2H), 8.10
(s, 1H), 10.32 (s, 1H).
(k) 5-(3-Chloro-phenyl)-furan-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]-phenyl}-amide (90)
(i) 5-Bromo-furan-2-carboxylic acid
[3-(2-cyano-vinyl)-phenyl]-amide
##STR00211##
[0852] 5-Bromo-furan-2-carboxylic acid (716 mg, 3.75 mmol) was
coupled to aniline (88) (540 mg, 3.75 mmol) using Method C. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane, to give the title compound.
[0853] Yield: 451 mg, 38%; LC/MS t.sub.r 1.39 min; MS(ES+) m/z 317,
319 (M+H).
(ii) 5-(3-Chloro-phenyl)-furan-2-carboxylic acid
[3-(2-cyano-vinyl)-phenyl]-amide
##STR00212##
[0855] The furyl bromide (150 mg, 0.47 mmol) was coupled to
3-chloro-phenylboronic acid (81 mg, 0.52 mmol) using Method E. The
crude residue was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0856] Yield: 61 mg, 37%; LC/MS t.sub.r 1.65 min; MS(ES+) m/z 349,
351 (M+H).
(iii) 5-(3-Chloro-phenyl)-furan-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]-phenyl}-amide (90)
##STR00213##
[0858] The nitrile (61 mg, 0.18 mmol) was treated with TMSN.sub.2
and Bu.sub.2SnO using Method L. After work-up, the residue was
dissolved in MeOH (2 ml) and washed with heptane (3.times.3 ml).
The layers were separated and the MeOH was removed in vacuo to give
the title compound.
[0859] Yield: 18 mg, 26%; LC/MS t.sub.r 1.48 min; MS(ES+) m/z 392,
394 (M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz, DMSO): .delta.
7.20-7.27 (m, 2H), 7.48-7.70 (m, 5H), 7.67 (d, 1H), 7.77 (d, 1H),
7.90 (d, 1H), 8.05 (d, 2H), 10.34 (s, 1H).
(l) 6-Phenyl-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (92)
(i) 6-Bromo-pyridine-2-carboxylic acid (3-cyanomethyl-phenyl)-amide
(91)
##STR00214##
[0861] 6-Bromo-pyridine-2-carboxylic acid (1.60 g, 12.1 mmol) was
coupled to aniline (91) (2.44 g, 12.1 mmol) using Method C. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[0862] Yield: 1.20 g, 31%; LC/MS t.sub.r 1.38 min; MS(ES+) m/z 316,
318 (M+H).
(ii) 6-Phenyl-pyridine-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00215##
[0864] The pyridyl bromide (91) (150 mg, 0.47 mmol) was coupled to
phenylboronic acid (64 mg, 0.52 mmol) using Method E. The crude
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[0865] Yield: 50 mg, 34%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 314
(M+H).
(iii) 6-Phenyl-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethyl)-phenyl]-amide (92)
##STR00216##
[0867] The nitrile (50 mg, 0.16 mmol) was treated with TMSN.sub.3
and Bu.sub.2SnO using Method L. After a first treatment, TMSN.sub.3
(73 mg, 0.64 mmol) and Bu.sub.2SnO (8 mg, 0.032 mmol) were added,
and the mixture was heated in the microwave for a further 20 min.
After work-up, the residue was dissolved in MeOH (2 ml) and washed
with heptane (3.times.3 ml). The layers were separated and the MeOH
was removed in vacuo. The solid was then triturated with heptane
(4.times.2 ml) to give the title compound.
[0868] Yield: 14 mg, 25%; LC/MS t.sub.r 1.47 min; MS(ES+) m/z 357
(M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz, DMSO): .delta. 4.09
(s, 2H), 6.85 (d, 1H), 7.15 (t, 1H), 7.27-7.39 (m, 3H), 7.58-7.63
(m, 2H), 7.86-7.96 (m, 2H), 8.03 (d, 1H), 8.12 (d, 2H), 10.31 (s,
1H).
(m) 6-(4-Fluoro-phenyl)-pyridine-2-carboxylicacid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (93)
(i) 6-(4-Fluoro-phenyl)-pyridine-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00217##
[0870] The pyridyl bromide (91) (150 mg, 0.47 mmol) was coupled to
4-fluoro-phenylboronic acid (73 mg, 0.52 mmol) using Method E. The
crude residue was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0871] Yield: 90 mg, 58%; LC/MS t.sub.r 1.55 min; MS(ES+) m/z 332
(M+H).
(ii) 6-(4-Fluoro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (93)
##STR00218##
[0873] The nitrile (90 mg, 0.27 mmol) was treated with TMSN.sub.3
and Bu.sub.2SnO using Method L. After a first treatment, further
TMSN.sub.3 (125 mg, 1.08 mmol) and Bu.sub.2SnO (14 mg, 0.054 mmol)
were added and the mixture was heated in the microwave for a
further 20 min. After work-up, the residue was dissolved in MeOH (2
ml) and washed with heptane (3.times.3 ml). The layers were
separated and the MeOH was removed in vacuo. The solid was then
triturated with heptane (4.times.2 ml) to give the title
compound.
[0874] Yield: 59 mg, 58%; LC/MS t.sub.r 1.48 min; MS(ES+) m/z 375
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO): .delta. 4.25
(s, 2H), 7.02 (d, 1H), 7.29-7.36 (m, 3H), 7.71-7.78 (m, 2H),
7.99-8.11 (m, 2H), 8.19 (d, 1H), 8.34-8.40 (m, 2H), 10.49 (s,
1H).
(n) 6-(3-Fluoro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (94)
(i) 6-(3-Fluoro-phenyl)-pyridine-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00219##
[0876] The pyridyl bromide (91) (150 mg, 0.47 mmol) was coupled to
3-fluoro-phenylboronic acid (73 mg, 0.52 mmol) using Method E. The
crude residue was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0877] Yield: 144 mg, 93%; LC/MS t.sub.r 1.56 min; MS(ES+) m/z 332
(M+H).
(ii) 6-(3-Fluoro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (93)
##STR00220##
[0879] The nitrile (144 mg, 0.44 mmol) was treated with TMSN.sub.2
and Bu.sub.2SnO using Method L. After a first treatment, TMSN.sub.3
(200 mg, 1.74 mmol) and Bu.sub.2SnO (21 mg, 0.087 mmol) were added
and the mixture was heated in the microwave for a further 20 min.
After work-up, the residue was dissolved in MeOH (2 ml) and washed
with heptane (3.times.3 ml). The layers were separated and the MeOH
was removed in vacuo. The solid was then triturated with heptane
(4.times.2 ml) to give the title compound.
[0880] Yield: 92 mg, 56%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 375
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO): .delta. 4.53
(s, 2H), 7.29 (d, 1H), 7.51-7.62 (m, 2H), 7.75-7.83 (m, 1H),
7.99-8.05 (m, 2H), 8.29-8.40 (m, 3H), 8.49-8.55 (m, 2H), 10.78 (s,
1H).
(o) 6-(4-Chloro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (95)
(i) 6-(4-Chloro-phenyl)-pyridine-2-carboxylic acid
(3-cyanomethyl-phenyl)-amide
##STR00221##
[0882] The pyridyl bromide (91) (150 mg, 0.47 mmol) was coupled to
4-chloro-phenylboronic acid (81 mg, 0.52 mmol) using Method E. The
crude residue was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0883] Yield: 113 mg, 691; LC/MS t.sub.r 1.62 min; MS(ES+) m/z 348,
350 (M+H).
(ii) 6-(4-Chloro-phenyl)-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5ylmethyl)-phenyl]-amide (95)
##STR00222##
[0885] The nitrile (113 mg, 0.33 mmol) was treated with TMSN.sub.3
and Bu.sub.2SnO using Method L. After a first treatment, TMSN.sub.3
(150 mg, 1.30 mmol) and Bu.sub.2SnO (16 mg, 0.065 mmol) were added
and the mixture was heated in the microwave for a further 20 min.
After work-up, the residue was dissolved in MeOH (2 ml) and washed
with heptane (3.times.3 ml). The layers were separated and the MeOH
was removed in vacuo. The solid was then triturated with heptane
(4.times.2 ml) to give the title compound.
[0886] Yield: 78 mg, 60%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 391,
393 (M+H); HPLC Purity: 97%; .sup.1H NMR (400 MHz, DMSO): .delta.
4.23 (s, 2H), 6.96 (d, 1H), 7.27 (t, 1H), 7.50 (d, 2H), 7.68-7.74
(m, 2H), 7.99-8.08 (m, 2H), 8.15 (d, 1H), 8.31 (d, 2H), 10.45 (s,
1H).
Example 9
(a) 5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzofuran-2-carboxylic
acid (96)
(i) 5-Nitro-benzofuran-2-carboxylic acid ethyl ester
##STR00223##
[0888] 5-Nitro-benzofuran-2-carboxylic acid (500 mg, 2.41 mmol) was
esterified with EtOH using Method A to give the title compound.
[0889] Yield: 488 mg, 86%; LC-MS t.sub.r 1.44 min; MS(ES+) m/z
(M+H) not present.
(ii) 5-Amino-benzofuran-2-carboxylic acid ethyl ester
##STR00224##
[0891] 5-Nitro-benzofuran-2-carboxylic acid ethyl ester (150 mg,
0.64 mmol) was reduced using Method J to give the title
compound.
[0892] Yield: 65 mg, 50%; LC-MS t.sub.r 0.87 min; MS(ES+) m/z 206
(M+H).
(iii) 5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzofuran-2-carboxylic
acid ethyl ester
##STR00225##
[0894] Carboxylic acid (56) (60 mg, 0.32 mmol) was coupled to
5-amino-benzofuran-2-carboxylic acid ethyl ester (65 mg, 0.32 mmol)
using Method C to give the title compound.
[0895] Yield: 35 mg, 29%; LC-MS t.sub.r 1.63 min; MS(ES+) m/z 376
(M+H).
(iv) 5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzofuran-2-carboxylic
acid (96)
##STR00226##
[0897] The ester (35 mg, 0.093 mmol) was hydrolysed using Method H
to give the title compound.
[0898] Yield: 25 mg, 77%; LC/MS t.sub.r 1.38 min; MS(ES+) m/z 348
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 7.02
(d, 1H), 7.36-7.53 (m, 4H), 7.61-7.64 (m, 2H), 7.75-7.80 (m, 1H)
7.95-7.99 (m, 2H), 8.20-8.21 (m, 1H).
(b)
5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzo[b]thiophene-2-carboxylic
acid (97)
(i) 5-Nitro-benzo[b]thiophene-2-carboxylic acid ethyl ester
##STR00227##
[0900] 5-Nitro-benzofuran-2-carboxylic acid (500 mg, 2.24 mmol) was
esterified with EtOH using Method A to give the title compound.
[0901] Yield: 497 mg, 88%; LC-MS t.sub.r 1.58 min; MS(ES+) m/z
(M+H) not present.
(ii) 5-Amino-benzo[b]thiophene-2-carboxylic acid ethyl ester
##STR00228##
[0903] 5-Nitro-benzothiophene-2-carboxylic acid ethyl ester (160
mg, 0.64 mmol) was reduced using Method J to give the title
compound.
[0904] Yield: 123 mg, 87%; LC-MS t.sub.r 0.98 min; MS(ES+) m/z 222
(M+H).
(iii)
5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzo[b]thiophene-2-carboxylic
acid ethyl ester
##STR00229##
[0906] Carboxylic acid (56) (105 mg, 0.56 mmol) was coupled to
5-amino-benzothiophene-2-carboxylic acid ethyl ester (123 mg, 0.56
mmol) using Method C to give the title compound.
[0907] Yield: 75 mg, 34%; LC-MS t.sub.r 1.72 min; MS(ES+) m/z 392
(M+H).
(iv)
5-[(5-Phenyl-furan-2-carbonyl)-amino]-benzo[b]thiophene-2-carboxylic
acid (97)
##STR00230##
[0909] The ester (75 mg, 0.19 mmol) was hydrolysed using Method H
to give the title compound.
[0910] Yield: 43 mg, 62%; LC/MS t.sub.r 1.47 min; MS(ES+) m/z 363
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, MeOD) .delta. 7.03
(d, 1H), 7.39-7.42 (m, 2H), 7.48-7.52 (m, 2H), 7.82-7.85 (m, 1H),
7.94-7.99 (m, 3H) 8.07-8.10 (m, 1H), 8.42-8.43 (m, 1H).
(c) 2-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-benzylidene}-butyric
acid (98)
(i) 2-(3-Nitro-benzylidene)-butyric acid ethyl ester
##STR00231##
[0912] 2-(3-Nitro-benzylidene)-butyric acid (500 mg, 2.27 mmol) was
esterified by dissolving in EtOH (12.5 ml), adding conc HCl (0.25
ml) and heating to reflux for 8 h. The solvents were evaporated in
vacuo to give the title compound.
[0913] Yield: 440 mg, 78%; LC-MS t.sub.r 1.64 min; MS(ES+) m/z
(M+H) not present.
(ii) 2-(3-Amino-benzylidene)-butyric acid ethyl ester
##STR00232##
[0915] 2-(3-Nitro-benzylidene)-butyric acid ethyl ester (230 mg,
0.92 mmol) was reduced using Method J to give the title
compound.
[0916] Yield: 186 mg, 92%; LC-MS t.sub.r 1.06 min; MS(ES+) m/z 220
(M+H).
(iii) 2-{3-[(5-Bromo-furan-2-carbonyl)-amino]-benzylidene}-butyric
acid ethyl ester
##STR00233##
[0918] 5-Bromo-furan-2-carboxylic acid (88 mg, 0.46 mmol) was
coupled to 2-(3-amino-benzylidene)-butyric acid ethyl ester (100
mg, 0.46 mmol) using Method C to give the title compound.
[0919] Yield: 132 mg, 73%; LC-MS t.sub.r 1.66 min; MS(ES+) m/z 392,
394 (M+H).
(iv) 2-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-benzylidene}-butyric
acid ethyl ester
##STR00234##
[0921] The furyl bromide (132 mg, 0.34 mmol) was coupled to
phenylboronic acid (45 mg, 0.37 mmol) using Method E. The residue
was purified by column chromatography eluting with 10% EtOAc in
heptane to give the title compound.
[0922] Yield: 36 mg, 27%; LC-MS t.sub.r 1.78 min; MS(ES+) m/z 390
(M+H).
(v) 2-{3-[(5-Phenyl-furan-2-carbonyl)-amino]-benzylidene}-butyric
acid (98)
##STR00235##
[0924] The ester (35 mg, 0.090 mmol) was hydrolysed using Method H
to give the title compound.
[0925] Yield: 7.6 mg, 23%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 362
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 1.23
(t, 3H), 3.33 (q, 2H) 7.01 (d, 1H), 7.20-7.23 (m, 1H), 7.39-7.52
(m, 5H), 7.67-7.70 (m, 2H) 7.95-7.98 (m, 3H).
(d)
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (100)
(i) 3-{3-[(5-Bromo-furan-2-carbonyl)-amino]-phenyl}-acrylic acid
ethyl ester (99)
##STR00236##
[0927] 5-Bromo-furan-2-carboxylic acid (150 mg, 0.78 mmol) was
coupled to aniline (60) (150 mg, 0.78 mmol) using Method C to give
the title compound.
[0928] Yield: 125 mg, 44%; LC-MS t.sub.r1.53 min; MS(ES+) m/z 364,
366 (M+H).
(ii)
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00237##
[0930] The furyl bromide (99) (125 mg, 0.34 mmol) was coupled to
3-fluoro-phenylboronic acid (48 mg, .times.0.41 mmol) acid using
Method E. The residue was purified by column chromatography eluting
with 20% EtOAc in heptane to give the title compound.
[0931] Yield: 96 mg, 74%; LC-MS t.sub.r 1.68 min; MS(ES+) m/z 380
(M+H)
(iii)
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (100)
##STR00238##
[0933] The ester (96 mg, 0.25 mmol) was hydrolysed using Method H
to give the title compound.
[0934] Yield: 58 mg, 66%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 352
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, DMSO) .delta. 6.51
(d, 1H), 7.22-7.63 (m, 7H), 7.83-8.01 (m, 4H), 10.31 (s, 1H), 12.43
(s, 1H).
(e)
3-{3-[(5-Benzo[1,3]dioxol-5-yl-furan-2-carbonyl)-amino]-phenyl}-acryli-
c acid (101)
##STR00239##
[0936] The furyl bromide (99) (100 mg, 0.30 mmol) was coupled to
3,4-(methylenedioxy)-phenylboronic acid (54 mg, 0.33 mmol) using
Method E. During this reaction, hydrolysis occurred. The crude
reaction mixture was diluted with H.sub.2O (4 ml) and extracted
with EtOAc (3.times.1 ml), then the aqueous layer was acidified
with 2M HCl until a white precipitate appeared and extracted with
DCM (3.times.1 ml). The organic layer was dried (MgSO.sub.4),
filtered and the solvent removed in vacuo. The solid was triturated
with TBME (2.times.2 ml) to give the title compound.
[0937] Yield: 27 mg, 24%; LC/MS t.sub.r 1.99 min; MS(ES+) m/z 378
(M+H); HPLC Purity: 93%; .sup.1H NMR (250 MHz; DMSO): .delta. 6.10
(s, 2H), 6.50 (d, 1H), 7.02-7.05 (m, 2H), 7.33-7.68 (m, 6H),
7.78-7.88 (m, 1H), 8.00 (s, 1H), 10.21 (s, 1H).
(f)
3-(3-{[5-(3,5-Bis-trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}phen-
yl)-acrylic acid (102)
(i)
3-(3-{[5-(3,5-Bis-trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}phen-
yl)-acrylic acid ethyl ester
##STR00240##
[0939] The furyl bromide (99) (70 mg, 0.19 mmol) was coupled to
3,5-bis-trifluoromethyl-phenylboronic acid (55 mg, 0.21 mmol) acid
using Method E, except that the reaction was heated at 100.degree.
C. The crude product was purified by column chromatography eluting
with a stepped gradient of 0-10% EtOAc in heptane to give the title
compound.
[0940] Yield: 45 mg, 47%; LC-MS t.sub.r 1.87 min; MS(ES+) m/z 498
(M+H).
(ii)
3-(3-{[5-(3,5-Bis-trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}phe-
nyl)-acrylic acid (102)
##STR00241##
[0942] To a solution of the ester (45 mg, 0.09 mmol) in THF (1 ml)
and MeOH (1 ml) was added 1M NaOH (2 ml) and the resulting solution
was stirred for 1 h at 4.0.degree. C. The THF and MeOH were removed
in vacuo then 2M HCl was added until a white precipitate formed.
The aqueous layer was extracted with DCM (3.times.1 ml). The
organic layer was dried (MgSO.sub.4), filtered and the solvent was
removed in vacuo. The solid was triturated with 50% DCM in heptane
(2.times.2 ml) and 50% MeOH in H.sub.2O (2.times.2 ml) to give the
title compound.
[0943] Yield: 15 mg, 36%; LC/MS t.sub.r 2.23 min; MS(ES+) m/z 470
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 6.52
(d, 1H), 7.25-7.28 (m, 1H), 7.30-7.37 (m, 3H), 7.59 (d, 1H),
7.69-7.73 (m, 1H), 7.38 (d, 2H), 8.50 (s, 2H).
(g) 3-{3-[(5-Biphenyl-3-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (103)
(i) 3-{3-[(5-Biphenyl-3-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00242##
[0945] Bromo-derivative (99) (70 mg, 0.19 mmol) was coupled to
biphenyl-3-boronic acid (42 mg, 0.21 mmol) acid using Method E,
except that the reaction was heated at 100.degree. C. The crude
product was purified by column chromatography eluting with a
stepped gradient of 0-10% EtOAc in heptane to give the title
compound.
[0946] Yield: 33 mg, 39%; LC-MS t.sub.r 1.86 min; MS(ES+) m/z 438
(M+H).
(ii)
3-{3-[(5-Biphenyl-3-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (103)
##STR00243##
[0948] To a solution of the ester (33 mg, 0.075 mmol) in THF (2 ml)
and MeOH (2 ml) was added 1M NaOH (4 ml) and the resulting solution
was stirred for 1 h at 40.degree. C. The THF and MeOH were removed
in vacuo and the aqueous layer was extracted with TBME (2.times.2
ml). The aqueous layer was acidified with 6M HCl until a white
precipitate formed. This was then extracted with TBME (3.times.2
ml). The organic layer was dried (MgSO.sub.4), filtered and the
solvent was removed in vacuo. The residue was suspended in H.sub.2O
(1 ml), MeOH (1 ml) and heptane (1 ml) and the resulting solid was
filtered and dried in vacuo to give the title compound.
[0949] Yield: 15 mg, 46%; LC/MS t.sub.r 2.21 min; MS(ES+) m/z 410
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz; MeOD): .delta. 6.72
(d, 1H), 7.29 (d, 1H), 7.56-7.72 (m, 6H), 7.73-7.79 (t, 1H),
7.83-7.97 (m, 4H), 8.01 (d, 1H), 8.12 (d, 1H), 8.19 (s, 1H), 8.43
(s, 1H).
(h)
3-(3-{[5-(3-Benzyloxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (104)
(i)
3-(3-{[5-(3-Benzyloxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00244##
[0951] The furyl bromide (99) (100 mg, 0.28 mmol) was coupled to
3-benzyloxy-phenylboronic acid (69 mg, 0.30 mmol) acid using Method
E, except that the reaction was heated at 85.degree. C. The crude
product was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[0952] Yield: 86 mg, 67%; LC-MS t.sub.r 1.83 min; MS(ES+) m/z 468
(M+H).
(ii)
3-(3-{[5-(3-Benzyloxy-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acryli-
c acid (104)
##STR00245##
[0954] The ester (86 mg, 0.18 mmol) was hydrolysed using Method H
to give the title compound.
[0955] Yield: 36 mg, 45%; LC/MS t.sub.r 1.65 min; MS(ES+) m/z 440
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, DMSO) .delta. 5.19
(s, 2H), 6.51 (d, 1H), 6.67-7.05 (m, 2H), 7.28-7.45 (m, 7H),
7.46-7.54 (m, 3H), 7.62-7.73 (m, 2H), 7.80-7.88 (m, 1H), 8.01 (s,
1H).
(i)
3-(3-{[5-(2-Fluoro-biphenyl-4-yl)-furan-2-carbonyl]-amino}-phenyl)-acr-
ylic acid (105)
(i)
3-(3-{[5-(2-Fluoro-biphenyl-4-yl)-furan-2-carbonyl]-amino}-phenyl)-acr-
ylic acid ethyl ester
##STR00246##
[0957] The furyl bromide (99) (100 mg, 0.28 mmol) was coupled to
2-Fluoro-biphenyl-4-boronic acid (65 mg, 0.30 mmol) acid using
Method E, except that the reaction was heated at 85.degree. C. The
crude product was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0958] Yield: 67 mg, 54%; LC-MS t.sub.r 1.89 min; MS(ES+) m/z 456
(M+H).
(ii)
3-(3-{[5-(2-Fluoro-biphenyl-4-yl)-furan-2-carbonyl]-amino}-phenyl)-ac-
rylic acid (105)
##STR00247##
[0960] The ester (67 mg, 0.15 mmol) was hydrolysed using Method H
to give the title compound.
[0961] Yield: 43 mg, 67%; LC/MS t.sub.r 2.23 min; MS(ES+) m/z 440
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, DMSO) .delta. 6.53
(d, 1H), 7.38 (d, 1H), 7.42-7.59 (m, 6H), 7.60-7.73 (m, 4H), 7.87
(d, 1H), 7.94 (d, 1H), 8.01-8.09 (m, 2H), 10.35 (s, 1H), 12.52
(broad s, 1H).
(j) 3-{3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (107)
(i) 3-[3-(5-Bromo-2-fluoro-benzoylamino)-phenyl]-acrylic acid ethyl
ester (106)
##STR00248##
[0963] 5-Bromo-2-fluorobenzoic acid (330 mg, 1.5 mmol) was coupled
to aniline (99) (290 mg, 1.5 mmol) using Method C to give the title
compound.
[0964] Yield: 525 mg, 89%; LC-MS t.sub.r1.61 min; MS(ES+) m/z 392,
394 (M+H).
(ii) 3-{3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00249##
[0966] The phenyl bromide (106) (100 mg, 0.25 mmol) was coupled to
phenylboronic acid (34 mg, .times.0.28 mmol) using Method E. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[0967] Yield: 38 mg, 39%; LC-MS t.sub.r 1.72 min; MS(ES+) m/z 390
(M+H).
(iii) 3-{3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (107)
##STR00250##
[0969] The ester (38 mg, 0.098 mmol) was hydrolysed using Method H
to give the title compound.
[0970] Yield: 29 mg, 82%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 362
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 6.54
(d, 1H), 7.34-7.53 (m, 6H), 7.66-7.88 (m, 5H), 7.99-8.03 (m,
2H).
(k)
3-{3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (108)
(i)
3-{3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00251##
[0972] The phenyl bromide (106) (100 mg, 0.25 mmol) was coupled to
3-fluoro-phenylboronic acid (39 mg, 0.28 mmol) using Method E. The
crude product was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0973] Yield: 17 mg, 17%; LC-MS t.sub.r 1.73 min; MS(ES+) m/z 408
(M+H).
(ii)
3-{3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (108)
##STR00252##
[0975] The ester (17 mg, 0.042 mmol) was hydrolysed using Method H
to give the title compound.
[0976] Yield: 13 mg, 82%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 380
(M+H). HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 6.54
(d, 1H), 7.08-7.20 (m, 1H), 7.35-7.53 (m, 6H), 7.69 (d, 1H),
7.78-7.90 (m, 2H), 7.99-8.04 (m, 2H).
(l)
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (110)
(i) 3-{3-[(6-Bromo-pyridine-2-carbonyl)-amino]-phenyl}-acrylic acid
ethyl ester (109)
##STR00253##
[0978] 6-Bromo-pyridine-2-carboxylic acid (127 mg, 0.63 mmol) was
coupled to aniline (60) (120 mg, 0.63 mmol) using Method C to give
the title compound.
[0979] Yield: 201 mg, 85%; LC-MS t.sub.r1.62 min; MS(ES+) m/z 375,
377 (M+H).
(ii)
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryli-
c acid ethyl ester
##STR00254##
[0981] The pyridyl bromide (109) (100 mg, 0.27 mmol) was coupled to
3-fluoro-phenylboronic acid (41 mg, 0.29 mmol) using Method E. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[0982] Yield: 36 mg, 34%; LC-MS t.sub.r 1.79 min; MS(ES+) m/z 391
(M+H).
(iii)
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryl-
ic acid (110)
##STR00255##
[0984] The ester (36 mg, 0.092 mmol) was hydrolysed using Method H
to give the title compound.
[0985] Yield: 23 mg, 69%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 363
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta.
6.54-6.64 (m, 1H), 7.22-7.30 (m, 1H), 7.43-7.60 (m, 3H), 7.70-7.76
(m, 1H), 7.89-7.93 (m, 1H), 8.05-8.13 (m, 6H).
(m) 3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic
acid (111)
(i) {3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic
acid ethyl ester
##STR00256##
[0987] The phenyl bromide (78) (106 mg, 0.28 mmol) was coupled to
3-fluoro-phenylboronic acid (42 mg, 0.30 mmol) using Method E. The
crude product was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[0988] Yield: 66 mg, 60%; LC-MS t.sub.r 1.63 min; MS(ES+) m/z 396
(M+H).
(ii) 3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acetic
acid (111)
##STR00257##
[0990] The ester (66 mg, 0.17 mmol) was hydrolysed using Method H
to give the title compound.
[0991] Yield: 52 mg, 85%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 368
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 3.65
(s, 2H), 7.07-7.19 (m, 2H), 7.32-7.51 (m, 5H), 7.65-7.68 (m, 2H),
7.80-7.86 (m, 1H), 7.96-8.00 (m, 1H).
(n)
3-{3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (112)
(i) 4,4'-Difluoro-biphenyl-3-carboxylic acid
##STR00258##
[0993] 5-Bromo-2-fluorobenzoic acid (250 mg, 1.14 mmol) was coupled
to 4-fluoro-phenylboronic acid (192 mg, 1.37 mmol) using Method E
to give the title compound. No chromatography was necessary.
[0994] Yield: 209 mg, 78%; LC-MS t.sub.r1.36 min; MS(ES+) m/z (M+H)
not present.
(ii)
3-{3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00259##
[0996] 4,4'-Difluoro-biphenyl-3-carboxylic acid (100 mg, 0.43 mmol)
was coupled to aniline (60) (82 mg, 0.43 mmol) using Method C to
give the title compound.
[0997] Yield: 119 mg, 68%; LC-MS t.sub.r 1.73 min; MS(ES+) m/z 408
(M+H).
(iii)
3-{3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (112)
##STR00260##
[0999] The ester (119 mg, 0.29 mmol) was hydrolysed using Method H
to give the title compound.
[1000] Yield: 85 mg, 77%; LC/MS t.sub.r 1.56 min; MS(ES+) m/z 380
(M+H); HPLC Purity: 98%; .sup.1H NMR (250 MHz, MeOD) .delta. 6.53
(d, 1H), 7.19-7.27 (m, 2H), 7.33-7.49 (m, 3H), 7.67-7.86 (m, 5H),
7.96-8.00 (m, 2H).
(o)
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (113)
(i)
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid ethyl ester
##STR00261##
[1002] The pyridyl bromide (77) (100 mg, 0.28 mmol) was coupled to
3-fluoro-phenylboronic acid (42 mg, 0.30 mmol) using Method E. The
crude product was purified by column chromatography eluting with
20% EtOAc in heptane to give the title compound.
[1003] Yield: 95 mg, 90%; LC-MS t.sub.r 1.69 min; MS(ES+) m/z 379
(M+H).
(ii)
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (113)
##STR00262##
[1005] The ester (95 mg, 0.25 mmol) was hydrolysed using Method H
to give the title compound.
[1006] Yield: 57 mg, 65%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 351
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, MeOD) .delta. 3.68
(s, 2H), 7.13-7.28 (m, 2H), 7.35-7.41 (m, 1H), 7.52-7.61 (m, 1H),
7.76-7.79 (m, 2H), 8.01-8.21 (m, 5H).
(p) 3-{3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acrylic
acid (115)
(i) 3-{3-[(2-Chloro-thiazole-4-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester (114)
##STR00263##
[1008] Carboxylic acid (79) (220 mg, 1.34 mmol) was coupled to
aniline (60) (257 mg, 1.34 mmol) using Method C to give the title
compound.
[1009] Yield: 260 mg, 57%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 337
(M+H).
(ii) 3-{3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00264##
[1011] The chloro thiazole (114) (80 mg, 0.24 mmol) was coupled to
phenylboronic acid (32 mg, 0.26 mmol) using Method E, except that
the reaction mixture was heated for a total of 4 h. The crude
residue was purified by column chromatography eluting with 25%
EtOAc in heptane to give the title compound.
[1012] Yield: 52 mg, 57%; LC/MS t.sub.r 1.76 min; MS(ES+) m/z 379
(M+H).
(iii) 3-{3-[(2-Phenyl-thiazole-4-carbonyl)-amino]-phenyl}-acrylic
acid (115)
##STR00265##
[1014] The ester (52 mg, 0.14 mmol) was hydrolysed using Method H
to give the title compound.
[1015] Yield: 31 mg, 63%; LC/MS t.sub.r 2.06 min; MS(ES+) m/z 351
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, DMSO) .delta. 6.53
(d, 1H), 7.44-7.47 (m, 2H), 7.55-7.61 (m, 4H), 7.96-8.01 (m, 1H),
8.13-8.21 (m, 3H), 8.53 (s, 1H), 10.33 (s, 1H).
(q)
3-(3-{[2-(3-Fluoro-phenyl)-thiazole-4-carbonyl]-amino}-phenyl)-acrylic
acid (116)
(i)
3-(3-{[2-(3-Fluoro-phenyl)-thiazole-4-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00266##
[1017] The chloro thiazole (114) (80 mg, 0.24 mmol) was coupled to
3-fluoro-phenylboronic acid (42 mg, 0.30 mmol) using Method E,
except that the reaction mixture was heated for a total of 12 h.
The crude residue was purified by column chromatography eluting
with 20% EtOAc in heptane to give the title compound.
[1018] Yield: 35 mg, 37%; LC/MS t.sub.r 1.76 min; MS(ES+) m/z 397
(M+H).
(ii)
3-(3-{[2-(3-Fluoro-phenyl)-thiazole-4-carbonyl]-amino}-phenyl)-acryli-
c acid (116)
##STR00267##
[1020] The ester (35 mg, 0.088 mmol) was hydrolysed using Method H
to give the title compound.
[1021] Yield: 6.3 mg, 19%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 369
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz, d.sup.6-Acetone)
.delta. 6.57 (d, 1H), 7.52-7.40 (m, 1H), 7.49 (d, 2H), 7.56-7.74
(m, 2H), 7.93-8.06 (m, 3H), 8.22 (s, 1H), 8.48 (s, 1H), 10.14 (s,
1H).
(r) [3-(Biphenyl-3-ylcarbamoyl)-phenyl]-acetic acid (117)
(i) Biphenyl-3-ylamine
##STR00268##
[1023] Bromobenzene (300 mg, 1.91 mmol) was coupled to
3-amino-phenylboronic acid (355 mg, 2.29 mmol) using Method E. The
crude residue was re-dissolved in EtOAc (8 ml) and washed with
saturated NaHCO.sub.3 (3.times.8 ml). The organic layer was
extracted with 1.2M HCl (1.times.8 ml) then basified with 6M NaOH
until a white precipitate formed. This was then extracted with
EtOAc (3.times.10 ml). The combined organic layers were dried
(MgSO.sub.4), filtered and the solvent removed in vacuo to give the
title compound. Yield: 297 mg, 92%; LC/MS t.sub.r 0.96 min; MS(ES+)
m/z 170 (M+H).
(ii) 3-Cyanomethyl-benzonitrile
##STR00269##
[1025] 3-Bromomethyl-benzonitrile (150 mg, 0.76 mmol) was dissolved
in DMF (2 ml). KCN (55 mg, 0.84 mmol) was dissolved in the minimum
amount of water and was added to the reaction. The resulting
solution was stirred at 85.degree. C. overnight. The reaction
mixture was allowed to cool to rood temperature, EtOAc (5 ml) was
added, and the solution was washed with saturated NaHCO.sub.3
(4.times.10 ml). The organic layer was dried (MgSO.sub.4), filtered
and the solvent removed in vacuo to give the title compound. Yield:
90 mg, 83%; LC/MS t.sub.r 1.04 min; MS(ES+) m/z 143 (M+H).
(iii) 3-Carboxymethyl-benzoic acid
##STR00270##
[1027] 3-Cyanomethyl-benzonitrile (90 mg, 0.63 mmol) was suspended
in conc. HCl (3 ml), and heated to 80.degree. C. for 2 h. The
solvent was then removed in vacuo to give the crude product, which
was used without further purification.
[1028] Yield: 110 mg, 97%; LC/MS t.sub.r 0.71 min; MS(ES+) m/z 181
(M+H).
(iv) 3-Ethoxycarbonylmethyl-benzoic acid
##STR00271##
[1030] The phenylacetic acid (110 mg, 0.61 mmol) was esterified
with EtOH using Method A to give the crude product, which was used
without further purification.
[1031] Yield: 126 mg, 99%; LC/MS t.sub.r 1.13 min; MS(ES+) m/z 209
(M+H).
(v) [3-(Biphenyl-3-ylcarbamoyl)-phenyl]-acetic acid ethyl ester
##STR00272##
[1033] 3-Ethoxycarbonylmethyl-benzoic acid (126 mg, 0.61 mmol) was
coupled to biphenyl-3-ylamine (105 mg, 0.62 mmol) using Method C.
The residue was purified by column chromatography eluting with 100%
DCM to give the title compound.
[1034] Yield: 17 mg, 8%; LC/MS t.sub.r 1.64 min; MS(ES+) m/z 360
(M+H).
(vi) [3-(Biphenyl-3-ylcarbamoyl)-phenyl]-acetic acid (117)
##STR00273##
[1036] The ester (17 mg, 0.047 mmol) was hydrolysed with NaOH (34
mg, 0.85 mmol using Method G to give the title compound.
[1037] Yield: 7.8 mg, 50%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 332
(M+H); HPLC Purity: 96%; .sup.1H NMR (400 MHz; CDCl.sub.3): .delta.
3.78 (s, 2H), 7.37-7.42 (m, 1H), 7.44-7.59 (m, 6H), 7.66-7.76 (m,
3H), 7.88-7.94 (m, 2H), 8.04 (s, 1H).
(s)
1-Methyl-5-[(5-phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic
acid (118)
(i) 1-Methyl-5-nitro-1H-indole-2-carboxylic acid
##STR00274##
[1039] 5-Nitro-1H-indole-2-carboxylic acid ethyl ester (234 mg, 1
mmol) was dissolved in DMF (2 ml). NaH (32 mg, 1.4 mmol) was added
as a suspension in heptane (0.5 ml) and the mixture was stirred at
room temperature for 10 min. Iodomethane (170 mg, 1.2 mmol) was
added drop-wise and the solution was left stirring for 1 h. During
this reaction, hydrolysis occurred. The reaction mixture was
quenched with H.sub.2O (2 ml) and washed with EtOAc (3.times.1 ml).
The aqueous layer was acidified to pH 1 with conc. HCl until a
white precipitate formed and extracted with EtOAc (3.times.1 ml).
These organic layer were combined, dried (MgSO.sub.4), filtered and
the solvent removed in vacuo to give the title compound. Yield: 99
mg, 45%; LC/MS t.sub.r 1.24 min; MS(ES+) m/z (M+H) not present;
.sup.1H NMR (400 MHz; DMSO) .delta. 4.10 (s, 3H), 7.52 (s, 1H),
7.81 (d, 1H), 8.16-8.20 (m, 1H), 8.74 (d, 1H).
(ii) 1-Methyl-5-nitro-1H-indole-2-carboxylic acid methyl ester
##STR00275##
[1041] 1-Methyl-5-nitro-1H-indole-2-carboxylic acid (99 mg, 0.45
mmol) was esterified with MeOH using Method A to give the title
compound.
[1042] Yield: 70 mg, 66%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 235
(M+H).
(iii) 5-Amino-1-methyl-1H-indole-2-carboxylic acid methyl ester
##STR00276##
[1044] 1-Methyl-5-nitro-1H-indole-2-carboxylic acid methyl ester
(70 mg, 0.3 mmol) was dissolved in DMF (5 ml) and
SnCl.sub.2.2H.sub.2O (339 mg, 1.5 mmol) was added as a solid. The
resulting solution was stirred at 60.degree. C. for 4 h. After
cooling to room temperature, a pre-mixed aqueous solution of
saturated Rochelle's salt (3 ml) and saturated NaHCO.sub.3 (3 ml)
was added to the reaction mixture and the aqueous layer was
extracted with EtOAc (3.times.6 ml). The organic layer was washed
with H.sub.2O (3 ml), 1:1 NaHCO.sub.3: Rochelle's salt solution (3
ml), dried (MgSO.sub.4), filtered and the solvent was removed in
vacuo to give the title compound.
[1045] Yield: 25 mg, 41%; LC-MS t.sub.r 0.85 min; MS(ES+) m/z 205
(M+H).
(iv)
1-Methyl-5-[(5-phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic
acid methyl ester
##STR00277##
[1047] Carboxylic acid (56) (23 mg, 0.12 mmol) was coupled to
5-amino-1-methyl-1H-indole-2-carboxylic acid methyl ester (25 mg,
0.12 mmol) using Method D to give the title compound.
[1048] Yield: 31 mg, 69%; LC-MS t.sub.r 1.59 min; MS(ES+) m/z 375
(M+H).
(v)
1-Methyl-5-[(5-phenyl-furan-2-carbonyl)-amino]-1H-indole-2-carboxylic
acid (118)
##STR00278##
[1050] The ester (31 mg, 0.08 mmol) was dissolved in MeOH (2 ml)
and 1M NaOH (1 ml). The suspension was stirred at room temperature
for 1 h, upon which THF (2 ml) was added. 1M NaOH (1 ml) was added
after 1 h. The resulting solution was stirred for 30 min at room
temperature, then THF and MeOH were removed in vacuo. The basic
solution was extracted with EtOAc (2.times.1 ml) and DCM (2.times.1
ml). The organic layers were dried (MgSO.sub.4), filtered,
combined, and evaporated in vacuo to give the title compound.
[1051] Yield: 19 mg, 66%; LC/MS t.sub.r 1.50 min; MS(ES+) m/z 361
(M+H); HPLC Purity: 95%; .sup.1H NMR (400 MHz; MeOD) .delta. 4.00
(s, 3H), 6.89 (s, 1H), 6.92-7.02 (m, 1H), 7.25 (d, 1H), 7.22-7.46
(m, 4H), 7.42 (d, 1H), 7.80-7.88 (m, 3H).
Example 10
(a) 3-{3-[2-Oxo-2-(5-phenyl-furan-2-yl)-ethyl]-phenyl}-acrylic acid
(120)
(i) 2-Phenyl-furan (119)
##STR00279##
[1053] Bromobenzene (1.5 g, 9.55 mmol) was coupled to
2-furylboronic acid (1.75 g, 15.6 mmol) using Method E. The crude
compound was purified by column chromatography using a stepped
gradient of 5-10% EtOAc in heptane to give the title compound.
[1054] Yield: 1.23 g, 89%; LC/MS t.sub.r 1.55 min; MS(ES+) m/z
(M+H) not present; .sup.1H NMR (400 MHz; DMSO) .delta. 6.46-6.48
(m, 1H), 6.65 (d, 1H), 7.25 (t, 1H), 7.38 (t, 2H), 7.46-7.47 (m,
1H), 7.67 (d, 2H).
(ii) 2-(3-Bromo-phenyl)-1-(5-phenyl-furan-2-yl)-ethanone
##STR00280##
[1056] 2-Phenyl-furan (119) (50 mg, 0.28 mmol) and
(3-bromo-phenyl)-acetic acid (134 mg, 0.63 mmol) were dissolved in
ortho-dichlorobenzene (4 ml). P.sub.2O.sub.5 (202 mg, 1.42 mmol)
was added as a suspension in ortho-dichlorobenzene (2 ml). The
reaction mixture was heated to 80.degree. C. for 2 h and cooled to
room temperature overnight. After the addition of further
P.sub.2O.sub.5 (202 mg, 1.42 mmol), heating was resumed at
90.degree. C. for 3 h. The reaction mixture was cooled to 0.degree.
C. and quenched with H.sub.2O (15 ml). The organic layer was
separated and the aqueous layer was washed with DCM (3.times.10
ml). The combined organic layers were dried (MgSO.sub.4), filtered
and the DCM removed in vacuo. The ortho-dichlorobenzene solution
was loaded to a silica-gel column and flushed with heptane (100
ml). The title compound was then eluted with 10% EtOAc in
heptane.
[1057] Yield: 60 mg, 63%; LC/MS t.sub.r 1.72 min; MS(ES+) m/z 341,
343 (M+H).
(iii) 3-{3-[2-Oxo-2-(5-phenyl-furan-2-yl)-ethyl]-phenyl}-acrylic
acid methyl ester
##STR00281##
[1059] Acrylic acid methyl ester (15 mg, 0.18 mmol) and Et.sub.3N
(59 mg, 0.59 mmol) were added to a microwave tube. Palladium (II)
acetate (1.6 mg, 0.05 mmol) in MeCN solution (0.5 ml),
tri-o-tolyl-phosphine (4.5 mg, 0.015 mmol) in MeCN solution (0.5
ml), and the phenyl bromide (50 mg, 0.15 mmol) in MeCN solution (3
ml) were then added. The solution was heated in a CEM Discover
microwave for 2.times.15 min at 90.degree. C. (150 W, 250 psi). The
solvent was removed in vacuo and the residue was purified by column
chromatography eluting with 10% EtOAc in heptane to give the title
compound.
[1060] Yield: 22 mg, 42%; LC/MS t.sub.r 1.61 min; MS(ES+) m/z 347
(M+H).
(iv) 3-{3-[2-Oxo-2-(5-phenyl-furan-2-yl)-ethyl]-phenyl}-acrylic
acid (120)
##STR00282##
[1062] The ester (22 mg, 0.063 mmol) was dissolved in MeOH (1 ml),
THF (0.2 ml) and 1M NaOH (1 ml). The suspension was stirred at room
temperature for 1 h. The solution was extracted with EtOAc
(2.times.1 ml). Further 1M NaOH was added (1 ml) and extraction was
repeated with EtOAc (2.times.1 ml). The aqueous layer was acidified
to pH 1 with conc. HCl and extracted with EtOAc (2.times.1 ml). The
organic layer was filtered through MgSO.sub.4 and the solvent
removed in vacuo. The solid was triturated with DCM (0.5 ml) to
give the title compound.
[1063] Yield: 1.3 mg, 6%; LC/MS t.sub.r 1.44 min; MS(ES+) m/z 333
(M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz; MeOD) .delta. 4.29
(s, 2H), 6.53 (d, 1H), 7.05 (d, 1H), 7.38-7.53 (m, 6H), 7.59 (d,
1H), 7.62-7.74 (m, 2H), 7.85-7.92 (m, 2H).
(b) 3-[3-(2-Phenyl-thiazol-4-ylmethoxy)-phenyl]-acrylic acid
(121)
(i) 3-(3-Hydroxy-phenyl)-acrylic acid methyl ester
##STR00283##
[1065] 3-(3-Hydroxy-phenyl)-acrylic acid (2 g, 12.2 mmol) was
esterified with MeOH using Method B to give the title compound.
[1066] Yield: 2.09 g, 96%; LC/MS t.sub.r 1.13 min; MS(ES+) m/z 179
(M+H).
(ii) 3-[3-(2-Phenyl-thiazol-4-ylmethoxy)-phenyl]-acrylic acid
methyl ester
##STR00284##
[1068] 3-(3-Hydroxy-phenyl)-acrylic acid methyl ester (85 mg, 0.48
mmol) was dissolved in dry DMF (1.5 ml) and NaH (14 mg, 0.60 mmol)
was added as a suspension in heptane (0.5 ml). The mixture was
stirred at room temperature for 10 min.
4-Chloromethyl-2-phenyl-thiazole (100 mg, 0.48 mmol) was added
portion-wise and the solution left stirring for 4 h. The reaction
mixture was quenched with H.sub.2O (2 ml) and extracted with EtOAc
(3.times.1 ml). The combined organic layers were washed with
H.sub.2O (3.times.1 ml), dried (MgSO.sub.4), filtered and the
solvent removed in vacuo to give a mixture of acid and ester, which
was used without further purification.
[1069] For the ester: LC/MS t.sub.r 1.64 min; MS(ES+) m/z 352
(M+H).
(iii) 3-[3-(2-Phenyl-thiazol-4-ylmethoxy)-phenyl]-acrylic acid
(122)
##STR00285##
[1071] The mixture (167 mg, 0.47 mmol) was stirred in MeOH (3 ml),
4M NaOH (3 ml) and THF (3 ml) for 30 min. The solution was
extracted with EtOAc (3.times.5 ml) and the aqueous layer was
acidified with conc. HCl until a white precipitate formed. This was
extracted with EtOAc (3.times.5 ml). The combined organic layers
were dried (MgSO.sub.4), filtered and the solvent removed in vacuo
to give the title compound.
[1072] Yield: 156 mg, 98% over 2 steps; LC/MS t.sub.r 1.58 min;
MS(ES+) m/z 338 (M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz;
DMSO): .delta. 5.23 (s, 2H), 6.5 (broad d, 1H), 7.02 (broad d, 1H),
7.09-7.18 (m, 2H), 7.22-7.35 (m, 2H), 7.42-7.58 (m, 3H), 7.78 (s,
1H), 7.89-7.99 (m, 2H).
(c) 3-[3-(2-Phenyl-thiazol-4-ylmethylsulfanyl)-phenyl]-acrylic acid
(122)
(i) 4-(3-Bromo-phenylsulfanylmethyl)-2-phenyl-thiazole
##STR00286##
[1074] NaH (53 mg, 2.2 mmol) was suspended in dry THF (1.5 ml)
under a stream of N.sub.2 and 3-bromo-benzenethiol (378 mg, 2 mmol)
was added dropwise to the suspension over 5 min.
4-Chloromethyl-2-phenyl-thiazole (419 mg, 2 mmol) was added and the
solution left stirring overnight. The reaction mixture was quenched
with a saturated K.sub.2CO.sub.3 solution (8 ml) and extracted with
EtOAc (3.times.4 ml). The combined organic layers were washed with
saturated K.sub.2CO.sub.3 solution (4 ml), dried (MgSO.sub.4),
filtered and the solvent removed in vacuo. The residue was purified
by column chromatography eluting with 20% EtOAc in heptane to give
the title compound.
[1075] Yield: 630 mg, 87%; LC/MS t.sub.r 1.85 min; MS(ES+) m/z 362,
364 (M+H).
(ii) 3-[3-(2-Phenyl-thiazol-4-ylmethylsulfanyl)-phenyl]-acrylic
acid methyl ester
##STR00287##
[1077] Acrylic acid methyl ester (28 mg, 0.33 mmol) and Et.sub.3N
(113 mg, 1.12 mmol) were added to a microwave tube. Palladium (II)
acetate (3 mg, 0.014 mmol) in MeCN solution (0.5 ml),
tri-o-tolyl-phosphine (4.5 mg, 0.028 mmol) in MeCN solution (0.5
ml), and the bromo-derivative (100 mg, 0.28 mmol) in MeCN solution
(1 ml) were then added. The solution was heated in a CEM Discover
microwave at 90.degree. C. (150 W, 250 psi) for a total of 4 h.
During this time, further palladium (II) acetate (4.times.3 mg,
0.056 mmol) was added. The solvent was removed under a stream of
N.sub.2 and H.sub.2O (3 ml) was added. The aqueous layer was
extracted with EtOAc (3.times.1 ml) and the organic layer washed
with H.sub.2O (1 ml), dried (MgSO.sub.4), filtered and the solvent
removed in vacuo. The residue was purified by column chromatography
eluting with 20% EtOAc in heptane to give the title compound.
[1078] Yield: 67 mg, 65%; LC/MS t.sub.r 1.78 min; MS(ES+) m/z 368
(M+H).
(iii) 3-[3-(2-Phenyl-thiazol-4-ylmethylsulfanyl)-phenyl]-acrylic
acid (122)
##STR00288##
[1080] The ester (67 mg, 0.18 mmol) was hydrolysed using Method H
to give the title compound.
[1081] Yield: 39 mg, 61%; LC/MS t.sub.r 1.61 min; MS(ES+) m/z 354
(M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz; MeOD): .delta. 4.38
(s, 2H), 6.48 (d, 1H), 7.25-7.53 (m, 7H), 7.57-7.70 (m, 2H),
7.89-7.99 (m, 2H).
(d)
3-{3-[(5-Adamantan-1-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (123)
(i) 5-Adamantan-1-yl-furan-2-carboxylic acid methyl ester
##STR00289##
[1083] Furan-2-carboxylic acid methyl ester (500 mg, 3.97 mmol) and
1-bromo-adamantane (853 mg, 3.97 mmol) were dissolved in
ortho-dichlorobenzene (6 ml) and cooled to 0.degree. C. before
adding AlCl.sub.2 (1.06 g, 7.94 mmol) as a solid. The reaction
mixture was allowed to warm up to room temperature, stirred for 4
h, then heated to 40.degree. C. for 2 h and left standing at room
temperature overnight. The reaction mixture was cooled to 0.degree.
C. and quenched with H.sub.2O (10 ml). The organic layer was
separated and the aqueous layer was extracted with DCM (3.times.20
ml). The combined organic layers were dried (MgSO.sub.4), filtered
and the DCM removed in vacuo. The ortho-dichlorobenzene solution
was loaded to a silica-gel column and flushed with heptane (100
ml). The title compound was then eluted using a stepped gradient of
0-10% EtOAc in heptane.
[1084] Yield: 503 mg, 49%; LC/MS t.sub.r 1.84 min; MS(ES+) m/z 261
(M+H).
(ii) 5-Adamantan-1-yl-furan-2-carboxylic acid
##STR00290##
[1086] The ester (503 mg, 1.93 mmol) was dissolved in THF (3 ml)
and 1M NaOH (3 ml). The suspension was stirred at room temperature
for 2 h. MeOH (3 ml) and 1M NaOH (3 ml) were added, and the
suspension was heated to 40.degree. C. for 1.5 h. THF and MeOH were
removed in vacuo upon which a precipitate appeared. The solid was
filtered, washed with 2M HCl (10 ml), and dried in vacuo to give
the title compound.
[1087] Yield: 458 mg, 96%; LC/MS t.sub.r 1.57 min; MS(ES+) m/z 288
(M+MeCN+H).
(iii)
3-{3-[(5-Adamantan-1-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00291##
[1089] 5-Adamantan-1-yl-furan-2-carboxylic acid (50 mg, 0.20 mmol)
was coupled to aniline (60) (43 mg, 0.22 mmol) using Method D to
give the title compound.
[1090] Yield: 84 mg, 100%; LC-MS t.sub.r1.97 min; MS(ES+) m/z 420
(M+H).
(iv)
3-{3-[(5-Adamantan-1-yl-furan-2-carbonyl)-amino]-phenyl}-acrylic
acid (123)
##STR00292##
[1092] The ester (84 mg, 0.20 mmol) was dissolved in MeOH (2 ml),
THF (2 ml) and 1M NaOH (4 ml). The suspension was heated to
40.degree. C. for 1 h. THF and MeOH were removed in vacuo, the
solution was acidified with 2M HCl (3 ml) and extracted with DCM
(3.times.2 ml). The organic layer was dried (MgSO.sub.4), filtered
and the solvent removed in vacuo. The solid was triturated with DCM
(2 ml) to give the title compound.
[1093] Yield: 35 mg, 45%; LC/MS t.sub.r 2.29 min; MS(ES+) m/z 392
(M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz; DMSO) .delta. 1.52
(s, 6H), 1.72 (s, 6H), 1.82 (s, 3H), 6.05 (s, 1H), 6.26 (d, 1H),
7.04 (d, 1H), 7.13-7.22 (m, 2H), 7.34 (d, 1H), 7.54 (d, 1H), 7.72
(s, 1H), 9.72 (s, 1H), 12.25 (broad s, 1H).
(e)
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (125)
(i) 3-(3-Amino-phenyl)-propionic acid ethyl ester (124)
##STR00293##
[1095] 3-(3-Aminophenyl)propionic acid (250 mg, 1.52 mmol) was
esterified with EtOH using Method A to give the title compound.
[1096] Yield: 260 mg, 89%; LC-MS t.sub.r 0.78 min; MS(ES+) m/z 194
(M+H).
(ii)
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid ethyl ester
##STR00294##
[1098] Carboxylic acid (67) (58 mg, 0.26 mmol) was coupled to
aniline (124) (50 mg, 0.26 mmol) using Method C. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1099] Yield: 62 mg, 60%; LC/MS t.sub.r 1.72 min; MS(ES+) m/z 398,
400 (M+H).
(iii)
3-(3-{[5-(3-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propioni-
c acid (125)
##STR00295##
[1101] The ester (62 mg, 0.16 mmol) was hydrolysed using Method H
to give the title compound.
[1102] Yield: 42 mg, 71%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 369,
371 (M+H); HPLC purity: 100%; .sup.1H NMR (400 MHz; DMSO): .delta.
2.51 (t, 2H), 2.79 (t, 2H), 6.96 (d, 1H), 7.2-7.3 (m, 2H), 7.35 (d,
1H), 7.41 (d, 1H), 7.48 (t, 1H), 7.54 (s, 1H), 7.59 (d, 1H), 7.90
(d, 1H), 8.07 (s, 1H), 10.15 (s, 1H).
(f)
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propio-
nic acid (126)
(i)
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propio-
nic acid ethyl ester
##STR00296##
[1104] Carboxylic acid (67) (67 mg, 0.26 mmol) was coupled to
aniline (124) (50 mg, 0.26 mmol) using Method C. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1105] Yield: 65 mg, 58%; LC/MS t.sub.r 1.86 min; MS(ES+) m/z 432,
434 (M+H).
(ii)
3-(3-{[5-(3,5-Dichloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propi-
onic acid (126)
##STR00297##
[1107] The ester (65 mg, 0.15 mmol) was hydrolysed using Method H
to give the title compound.
[1108] Yield: 46 mg, 76%; LC/MS t.sub.r 1.64 min; MS(ES+) m/z 404,
406 (M+H); HPLC purity: 90%; .sup.1H NMR (400 MHz; DMSO): .delta.
2.55 (t, 2H), 2.83 (t, 2H), 7.01 (d, 1H), 7.28 (t, 1H), 7.38 (d,
1H), 7.43 (d, 1H), 7.56 (s, 1H), 7.60 (t, 2H), 8.11 (s, 2H), 10.23
(s, 1H).
(g)
(3-{[5-(3,5-Difluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (127)
##STR00298##
[1110] The furyl bromide (16) (100 mg, 0.30 mmol) was coupled to
3,5-difluoro-phenylboronic acid (48 mg, 0.30 mmol) using Method E.
During this reaction, hydrolysis occurred. The residue was
extracted using Work-up E1 to give the acid. The residue was
purified by column chromatography eluting with 20% heptane: 75%
EtOAc: 5% AcOH to give the title compound.
[1111] Yield: 25 mg, 23%; LC/MS t.sub.r 1.47 min; MS(ES+) m/z 358
(M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz; DMSO): .delta. 3.64
(s, 2H), 7.10 (d, 1H), 7.31-7.41 (m, 2H), 7.44 (q, 2H), 7.68 (s,
1H), 7.75 (d, 1H), 7.87 (d, 2H), 10.29 (s, 1H).
(h)
(3-{[5-(3-fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acetic
acid (128)
##STR00299##
[1113] The furyl bromide (16) (100 mg, 0.30 mmol) was coupled to
3-fluoro-phenylboronic acid (42 mg, 0.30 mmol) using Method E.
During this reaction, hydrolysis occurred. The residue was
extracted using Work-up E1 to give the title compound.
[1114] Yield: 26 mg, 25%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 339
(M+H); HPLC Purity: 91%; .sup.1H NMR (400 MHz; DMSO): .delta. 3.50
(s, 2H), 6.95 (d, 1H), 7.15 (t, 1H), 7.20 (d, 1H), 7.24 (t, 1H),
7.32 (d, 1H), 7.46 (q, 1H), 7.56 (s, 1H), 7.62 (d, 1H), 7.74 (d,
1H), 7.83 (d, 1H), 10.13 (s, 1H).
(i)
(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (129)
##STR00300##
[1116] The pyridyl bromide (77) (44 mg, 0.12 mmol) was coupled to
3-chloro-phenylboronic acid (20 mg, 0.13 mmol) using Method E.
During this reaction, hydrolysis occurred. The residue was
extracted using Work-up E1 to give the acid. The solid was further
purified by preparative HPLC to give the title compound.
[1117] Yield: 8 mg, 18%; LC/MS t.sub.r 1.51 min; MS(ES+) m/z 367,
369 (M+H); HPLC Purity: 99%; .sup.1H NMR (400 MHz; DMSO): .delta.
3.63 (s, 2H), 7.09 (d, 1H), 7.37 (t, 1H), 7.60 (m, 2H), 7.82 (m,
2H), 8.17 (m, 2H), 8.33 (m, 2H), 8.52 (s, 1H), 10.60 (s, 1H).
(j)
(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-aceti-
c acid (130)
##STR00301##
[1119] The pyridyl bromide (77) (44 mg, 0.12 mmol) was coupled to
3,5-dichloro-phenylboronic acid (20 mg, 0.10 mmol) using Method E.
During this reaction, hydrolysis occurred. The residue was
extracted using Work-up E1 to give the acid. The solid was further
purified by preparative HPLC to give the title compound.
[1120] Yield: 30 mg, 62%; LC/MS t.sub.r 1.63 min; MS(ES+) m/z 401,
403 (M+H); HPLC Purity: 99%; .sup.1H NMR (400 MHz; DMSO): .delta.
3.60 (s, 2H), 7.07 (d, 1H), 7.35 (t, 1H), 7.77 (m, 3H), 8.17 (m,
2H), 8.37 (d, 1H), 8.49 (s, 2H), 10.64 (s, 1H).
(k)
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acr-
ylic acid (132)
(i) 6-(3,5-Dichloro-phenyl)-pyridine-2-carboxylic acid (131)
##STR00302##
[1122] 6-Bromo-pyridine-2-carboxylic acid (500 mg, 2.47 mmol) was
coupled to 3,5-dichloro-phenylboronic acid (473 mg, 2.47 mmol) acid
using Method F to give the title compound.
[1123] Yield: 400 mg, 60%; LC/MS t.sub.r 1.47 min; MS(ES+) m/z 268,
270 (M+H).
(ii)
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-ac-
rylic acid ethyl ester
##STR00303##
[1125] Carboxylic acid (131) (50 mg, 0.19 mmol) was coupled to
aniline (60) (40 mg, 0.21 mmol) using Method D. The residue was
triturated with TBME (3 ml) to give the title compound.
[1126] Yield: 61 mg, 72%; LC/MS t.sub.r 1.98 min; MS(ES+) m/z 441,
443 (M+H).
(iii)
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-a-
crylic acid (132)
##STR00304##
[1128] The ester (61 mg, 0.14 mmol) was hydrolysed using Method M
to give the title compound.
[1129] Yield: 50 mg, 87%; LC/MS t.sub.r 1.73 min; MS(ES+) m/z 412,
414 (M+H); HPLC Purity: 89%; .sup.1H NMR (250 MHz; DMSO): .delta.
6.44 (d, 1H), 7.17 (d, 1H), 7.29 (d, 1H), 7.40 (t, 1H), 7.75 (s,
1H), 7.82 (d, 1H), 8.02 (s, 1H), 8.18 (d, 2H), 8.38 (q, 1H), 8.50
(s, 2H), 10.66 (s, 1H).
(l)
(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acet-
ic acid (133)
(i)
(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acet-
ic acid ethyl ester
##STR00305##
[1131] Carboxylic acid (131) (50 mg, 0.19 mmol) was coupled to
aniline (64) (40 mg, 0.21 mmol) using Method D. The residue was
triturated with TBME (3 ml) to give the title compound.
[1132] Yield: 29 mg, 34%; LC/MS t.sub.r 1.86 min; MS(ES+) m/z 445,
447 (M+H).
(ii)
(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-ace-
tic acid (133)
##STR00306##
[1134] The ester (29 mg, 0.07 mmol) was hydrolysed using Method M.
The solid was triturated with DCM (3 ml) to give the title
compound.
[1135] Yield: 27 mg, 100%; LC/MS t.sub.r 1.67 min; MS(ES+) m/z 416,
418 (M+H); HPLC Purity: 92%; .sup.1H NMR (250 MHz; DMSO): .delta.
3.82 (s, 2H), 6.07 (broad s, 1H), 6.85 (broad t.sub.r 3H), 7.50 (s,
1H), 7.78 (m, 4H), 8.11 (broad s, 1H), 8.32 (s, 1H).
(m)
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-pro-
pionic acid (134)
(i)
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-pro-
pionic acid ethyl ester
##STR00307##
[1137] Carboxylic acid (131) (50 mg, 0.19 mmol) was coupled to
aniline (124) (40 mg, 0.21 mmol) using Method D to give the
product, which was used without further purification.
[1138] Yield: 83 mg, 99%; LC/MS t.sub.r 1.90 min; MS(ES+) m/z 443,
445 (M+H).
(ii)
3-(3-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-pr-
opionic acid (134)
##STR00308##
[1140] The ester (83 mg, 0.19 mmol) was hydrolysed using Method M.
The residue was purified by preparative HPLC to give the title
compound.
[1141] Yield: 42 mg, 53%; LC/MS t.sub.r 1.66 min; MS(ES+) m/z 415,
417 (M+H); HPLC Purity: 96%; .sup.1H NMR (400 MHz; DMSO): .delta.
2.69 (t, 2H), 2.98 (t, 2H), 7.16 (d, 1H), 7.44 (t, 1H), 7.80-7.88
(m, 3H), 8.25-8.32 (m, 2H), 8.47 (d, 1H), 8.59 (s, 2H), 10.70 (s,
1H), 12.28 (s, 1H).
(n)
5-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-1H-indole-2-ca-
rboxylic acid (135)
(i)
5-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-1H-indole-2-ca-
rboxylic acid ethyl ester
##STR00309##
[1143] Carboxylic acid (131) (50 mg, 0.19 mmol) was coupled to
aniline (58) (42 mg, 0.21 mmol) using Method D to give the crude
product.
[1144] Yield: 85 mg, 99%; LC/MS t.sub.r 1.82 min; MS(ES+) m/z 454,
456 (M+H).
(ii)
5-{[6-(3,5-Dichloro-phenyl)-pyridine-2-carbonyl]-amino}-1H-indole-2-c-
arboxylic acid (135)
##STR00310##
[1146] The ester (85 mg, 0.19 mmol) was hydrolysed using Method M.
The residue was purified by preparative HPLC to give the title
compound.
[1147] Yield: 16 mg, 20%; LC/MS t.sub.r 1.61 min; MS(ES+) m/z 426,
428 (M+H); HPLC Purity: 99%; .sup.1H NMR (400 MHz; DMSO): .delta.
7.23 (s, 1H), 7.56 (d, 1H), 7.75 (dd, 1H), 7.85 (t, 1H), 8.27 (m,
3H), 8.47 (q, 1H), 8.61 (d, 2H), 10.73 (s, 1H).
(o)
3-(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (137)
(i) 6-(3-chloro-phenyl)-pyridine-2-carboxylic acid (136)
##STR00311##
[1149] 6-Bromo-pyridine-2-carboxylic acid (200 mg, 0.99 mmol) was
coupled to 3-chloro-phenylboronic acid (130 mg, 0.83 mmol) using
Method F to give the title compound.
[1150] Yield: 182 mg, 98%; LC/MS t.sub.r 1.32 min; MS(ES+) m/z 234,
236 (M+H).
(ii)
3-(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryli-
c acid ethyl ester
##STR00312##
[1152] Carboxylic acid (136) (44 mg, 0.19 mmol) was coupled with
aniline (60) (40 mg, 0.21 mmol) using Method D. The residue was
purified by column chromatography eluting with a stepped gradient
of 10-15% EtOAc in heptane to give the title compound.
[1153] Yield: 64 mg, 83%; LC/MS t.sub.r 1.87 min; MS(ES+) m/z 407,
409 (M+H).
(iii)
3-(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryl-
ic acid (137)
##STR00313##
[1155] The ester (64 mg, 0.16 mmol) was hydrolysed using Method M.
The residue was purified by preparative HPLC to give the title
compound.
[1156] Yield: 7 mg, 11%; LC/MS t.sub.r 1.98 min; MS(ES+) m/z 379,
381 (M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz; DMSO): .delta.
6.54 (d, 1H), 7.43-7.67 (m, 5H), 7.99 (d, 1H), 8.17 (m, 3H), 8.34
(m, 2H), 8.50 (s, 1H), 10.66 (s, 1H).
(p)
(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (138)
(i)
(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00314##
[1158] Carboxylic acid (136) (44 mg, 0.19 mmol) was coupled with
aniline (64) (40 mg, 0.2 mmol) using Method D. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1159] Yield: 50 mg, 64%; LC/MS t.sub.r 1.77 min; MS(ES+) m/z 411,
413 (M+H).
(ii)
(3-{[6-(3-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (138)
##STR00315##
[1161] The ester (50 mg, 0.12 mmol) was hydrolysed using Method M.
The residue was purified by preparative HPLC to give the title
compound.
[1162] Yield: 30 mg, 65%; LC/MS t.sub.r 1.51 min; MS(ES+) m/z 383,
385 (M+H); HPLC Purity: 99%; .sup.1H NMR (400 MHz; DMSO): .delta.
4.63 (s, 2H), 6.66 (dd, 1H), 7.24 (t, 1H), 7.44 (d, 1H), 7.53 (m,
3H), 8.03 (m, 2H), 8.25 (m, 2H), 8.41 (s, 1H), 10.49 (s, 1H).
(q)
{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (140)
(i) [3-(5-Bromo-2-fluoro-benzoylamino)-phenoxy]-acetic acid ethyl
ester (139)
##STR00316##
[1164] 5-Bromo-2-fluoro-benzoic acid (250 mg, 1.14 mmol) was
coupled to aniline (64) (245 mg, 1.25 mmol) using Method D. The
residue was purified by column chromatography eluting with a
stepped gradient of 10-15% EtOAc in heptane to give the title
compound.
[1165] Yield: 144 mg, 36%; LC/MS t.sub.r 1.52 min; MS(ES+) m/z 396,
398 (M+H).
(ii)
{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (140)
##STR00317##
[1167] The phenyl bromide (139) (50 mg, 0.13 mmol) was coupled to
3-chloro-phenylboronic acid (20 mg, 0.13 mmol) using Method E.
During this reaction, hydrolysis occurred and the residue was
extracted using Work-up E1. The crude product was then triturated
with TBME (2 ml), DCM (2 ml), and recrystallised from a hot 10%
EtOH in H.sub.2O mixture to give the title compound.
[1168] Yield: 2 mg, 4%; LC/MS t.sub.r 1.89 min; MS(ES+) m/z 400,
402 (M+H); HPLC Purity: 88%; .sup.1H NMR (400 MHz; DMSO) .delta.
3.95 (s, 2H), 6.45 (d, 1H), 7.10 (m, 2H), 7.20 (m, 1H), 7.30-7.50
(m, 3H), 7.65 (d, 1H), 7.75 (e, 1H), 7.80 (m, 1H), 7.90 (d, 1H),
10.35 (s, 1H).
(r)
3-{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid (142)
(i) 3-[3-(5-Bromo-2-fluoro-benzoylamino)-phenyl]-acrylic acid ethyl
ester (141)
##STR00318##
[1170] 5-Bromo-2-fluoro-benzoic acid (250 mg, 1.14 mmol) was
coupled to aniline (60) (240 mg, 1.26 mmol) using Method D. The
residue was purified by column chromatography eluting with a
stepped gradient of 10-15% EtOAc in heptane to give the title
compound.
[1171] Yield: 402 mg, 90%; LC/MS t.sub.r 1.64 min; MS(ES+) m/z 392,
394 (M+H).
(ii)
3-{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00319##
[1173] The phenyl bromide (141) (100 mg, 0.26 mmol) was coupled to
3-chloro-phenylboronic acid (40 mg, 0.26 mmol) using Method E. The
residue was purified by column chromatography eluting with 10%
EtOAc in heptane to give the title compound.
[1174] Yield: 109 mg, 99%; LC/MS t.sub.r 1.82 min; MS(ES+) m/z 424,
426 (M+H).
(iii)
3-{3-[(3'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acryli-
c acid (142)
##STR00320##
[1176] The ester (109 mg, 0.26 mmol) was hydrolysed using Method M
to give the title compound.
[1177] Yield: 80 mg, 78%; LC/MS t.sub.r 1.05 min; MS(ES+) m/z 396,
398 (M+H); HPLC Purity: 95%; .sup.1H NMR (400 MHz, DMSO): .delta.
6.60 (d, 1H), 7.40-7.75 (m, 6H), 7.90 (d, 2H), 8.00 (s, 1H), 8.10
(broad s, 2H), 8.20 (d, 1H), 10.80 (s, 1H).
(s)
{3-[(3',5'-Dichloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acet-
ic acid (143)
(i)
{3-[(3',5'-Dichloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acet-
ic acid ethyl ester
##STR00321##
[1179] The phenyl bromide (139) (50 mg, 0.13 mmol) was coupled to
3,5-dichloro-phenylboronic acid (24 mg, 0.13 mmol) using method E.
The residue was purified by column chromatography eluting with 10%
EtOAc in heptane to give the title compound.
[1180] Yield: 10 mg, 17%; LC/MS t.sub.r1.79 min; MS(ES+) m/z 462,
464 (M+H).
(ii)
{3-[(3',5'-Dichloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-ace-
tic acid (143)
##STR00322##
[1182] The ester (10 mg, 0.02 mmol) was hydrolysed using Method M
to give the title compound.
[1183] Yield: 4 mg, 46%; LC/MS t.sub.r1.09 min; MS(ES+) m/z 434,
436 (M+H); HPLC Purity: 91%; .sup.1H NMR (400 MHz; DMSO) .delta.
4.50 (s, 2H), 6.65 (d, 1H), 7.20 (t, 1H), 7.30 (broad s, 2H), 7.45
(t, 1H), 7.65 (s, 1H), 7.85 (s, 2H), 8.00 (m, 1H), 8.05 (d, 1H),
10.50 (s, 1H).
(t)
3-{3-[(3',5'-Dichloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acr-
ylic acid (144)
(i)
3-{3-[(3',5'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acryl-
ic acid ethyl ester
##STR00323##
[1185] The phenyl bromide (141) (100 mg, 0.26 mmol) was coupled to
3,5-dichloro-phenylboronic acid (40 mg, 0.21 mmol) using method E.
The residue was purified by column chromatography eluting with 10%
EtOAc in heptane to give the title compound.
[1186] Yield: 75 mg, 78%; LC/MS t.sub.r1.90 min; MS(ES+) m/z 458,
460 (M+H).
(ii)
3-{3-[(3',5'-Chloro-4-fluoro-biphenyl-3-carbonyl)-amino]-phenyl}-acry-
lic acid (144)
##STR00324##
[1188] The ester (75 mg, 0.16 mmol) was hydrolysed using Method M
to give the title compound.
[1189] Yield: 58 mg, 84%; LC/MS t.sub.r 1.66 min; MS(ES+) m/z 430,
432 (M+H); HPLC Purity: 89%; .sup.1H NMR (400 MHz, DMSO): .delta.
6.50 (d, 1H), 7.35-7.70 (m, 5H), 7.80 (d, 1H), 7.90 (s, 2H), 8.00
(broad s, 2H), 8.10 (m, 1H), 10.60 (s, 1H).
(u)
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (146)
(i) 5-(4-Chloro-phenyl)-furan-2-carboxylic acid (145)
##STR00325##
[1191] 5-Bromo-2-furoic acid (1 g, 5.25 mmol) was coupled to
4-chloro-phenylboronic acid (819 mg, 5.23 mmol) acid using Method E
to give the title compound.
[1192] Yield: 250 mg, 22%; LC/MS t.sub.r 1.34 min; MS(ES+) m/z 223,
225 (M+H). .sup.1H NMR (400 MHz, DMSO): .delta. 7.05 (d, 1H), 7.20
(d, 1H), 7.40 (d, 2H), 7.70 (d, 2H).
(ii)
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00326##
[1194] Carboxylic acid (145) (50 mg, 0.19 mmol) was coupled to
aniline (60) (43 mg, 0.23 mmol) using Method C. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1195] Yield: 66 mg, 87%; LC/MS t.sub.r 1.77 min; MS(ES+) m/z 396,
398 (M+H).
(iii)
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-acrylic
acid (146)
##STR00327##
[1197] The ester (66 mg, 0.17 mmol) was hydrolysed using Method M.
The residue was recrystallised from a hot 10% EtOH in H.sub.2O
mixture to give the title compound.
[1198] Yield: 40 mg, 64%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 368,
370 (M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO): .delta.
6.50 (d, 1H), 7.30 (d, 1H), 7.35-7.65 (m, 6H), 7.85 (m, 1H), 8.00
(m, 3H).
(v)
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (147)
(i)
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid ethyl ester
##STR00328##
[1200] Carboxylic acid (145) (58 mg, 0.26 mmol) was coupled to
aniline (124) (50 mg, 0.26 mmol) using Method C. During this
reaction, partial hydrolysis occurred. The acid was re-dissolved in
EtOAc (2 ml) and the organic layer was washed with 1M HCl
(2.times.1 ml), dried (Na.sub.2SO.sub.4), filtered and the solvent
removed in vacuo to give a mixture of acid and ester, which was
used without further purification.
[1201] For the ester: LC/MS t.sub.r 1.72 min; MS(ES+) m/z 398, 400
(M+H).
(ii)
3-(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (147)
##STR00329##
[1203] The mixture (103 mg, 0.26 mmol) was hydrolysed using Method
M. The solid was recrystallised from a hot 10% EtOH in H.sub.2O
mixture to give the title compound.
[1204] Yield: 40 mg, 41% over 2 steps; LC/MS t.sub.r 1.48 min;
MS(ES+) m/z 370, 372 (M+H); HPLC Purity: 100%; .sup.1H NMR (400
MHz, DMSO): .delta. 2.60 (t, 2H), 2.90 (t, 2H), 7.00 (d, 1H),
7.20-7.35 (m, 2H), 7.40 (1H), 7.50-7.70 (m, 4H), 8.05 (d, 2H),
10.20 (s, 1H).
(x)
3-(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (148)
##STR00330##
[1206] Carboxylic acid (76) (53 mg, 0.26 mmol) was coupled to
aniline (124) (50 mg, 0.26 mmol) using Method C. During this
reaction, hydrolysis occurred. The acid was re-dissolved in EtOAc
(2 ml) and the organic layer was washed with 1M HCl (2.times.1 ml),
dried (Na.sub.2SO.sub.4), filtered and the solvent removed in
vacuo. The solid was recrystallised from a hot 10% EtOH in H.sub.2O
mixture to give the title compound.
[1207] Yield: 40 mg, 43%; LC/MS t.sub.r 1.39 min; MS(ES+) m/z 354
(M+H); HPLC Purity: 93%; .sup.1H NMR (400 MHz, DMSO): .delta. 2.57
(t, 2H), 2.85 (t, 2H), 7.01 (d, 1H), 7.17 (d, 1H), 7.24-7.42 (m,
4H), 7.63 (t, 2H), 8.05 (2H), 10.14 (s, 1H).
(y)
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (150)
(i) 6-(4-Chloro-phenyl)-pyridine-2-carboxylic acid (149)
##STR00331##
[1209] 6-Bromo-pyridine-2-carboxylic acid (1 g, 4.95 mmol) was
coupled to 4-chloro-phenylboronic acid (775 mg, 4.96 mmol) acid
using Method F to give the title compound.
[1210] Yield: 900 mg, 78%; LC/MS t.sub.r 1.29 min; MS(ES+) m/z 234,
236 (M+H); .sup.1H NMR (400 MHz, DMSO): .delta. 7.50 (d, 2H), 8.00
(t, 1H), 8.05 (d, 1H), 8.15 (t, 3H).
(ii)
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid ethyl ester
##STR00332##
[1212] Carboxylic acid (149) (50 mg, 0.22 mmol) was coupled to
aniline (6) (39 mg, 0.22 mmol) using Method C. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1213] Yield: 28 mg, 32%; LC/MS t.sub.r 1.77 min; MS(ES+) m/z 395,
397 (M+H).
(iii)
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (150)
##STR00333##
[1215] The ester (28 mg, 0.07 mmol) was hydrolysed using Method M
to give the title compound.
[1216] Yield: 17 mg, 66%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 367,
369 (M+H); HPLC Purity: 99%; .sup.1H NMR (250 MHz; DMSO): .delta.
3.60 (s, 2H), 7.10 (d, 1H), 7.40 (t, 1H), 7.60 (d, 2H), 7.80 (s,
2H), 8.10-8.20 (m, 2H), 8.30 (d, 1H), 8.45 (d, 2H).
(z)
3-(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid (151)
(i)
3-(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00334##
[1218] Carboxylic acid (149) (50 mg, 0.21 mmol) was coupled to
aniline (60) (41 mg, 0.21 mmol) using Method C. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1219] Yield: 34 mg, 40%; LC/MS t.sub.r 1.88 min; MS(ES+) m/z 407,
409 (M+H).
(ii)
3-(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryli-
c acid (151)
##STR00335##
[1221] The ester (34 mg, 0.08 mmol) was hydrolysed using Method M
to give the title compound.
[1222] Yield: 15 mg, 50%; LC/MS t.sub.r 1.62 min; MS(ES+) m/z 379,
381 (M+H); HPLC Purity: 99%; .sup.1H NMR (250 MHz; DMSO): .delta.
6.60 (d, 1H), 7.45-7.60 (m, 2H), 7.60-7.70 (m, 3H), 8.05 (m, 1H),
8.10-8.25 (m, 3H), 8.35 (m, 1H), 8.50 (d, 2H), 10.65 (s, 1H).
(aa)
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (153)
(i) 6-(4-Fluoro-phenyl)-pyridine-2-carboxylic acid (152)
##STR00336##
[1224] 6-Bromo-pyridine-2-carboxylic acid (1 g, 4.95 mmol) was
coupled 4-fluoro-phenylboronic acid (693 mg, 4.95 mmol) acid using
Method F to give the title compound.
[1225] Yield: 900 mg, 83%; LC/MS t.sub.r 1.14 min; MS(ES+) m/z 218
(M+H); .sup.1H NMR (400 MHz, DMSO): .delta. 7.42 (t, 2H), 8.05 (d,
1H), 8.13 (t, 1H), 8.27 (d, 1H), 8.32 (t, 2H).
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid ethyl ester
##STR00337##
[1227] Carboxylic acid (152) (50 mg, 0.23 mmol) was coupled to
aniline (6) (42 mg, 0.23 mmol) using Method C. The residue was
purified by column chromatography eluting with 10% EtOAc in heptane
to give the title compound.
[1228] Yield: 53 mg, 61%; LC/MS t.sub.r 1.69 min; MS(ES+) m/z 379
(M+H).
(iii)
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acetic
acid (153)
##STR00338##
[1230] The ester (48 mg, 0.13 mmol) was hydrolysed using Method M
to give the title compound.
[1231] Yield: 40 mg, 88%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 351
(M+H); HPLC Purity: 99%; .sup.1H NMR (250 MHz; DMSO): .delta. 3.60
(s, 2H), 7.31-7.43 (m, 3H), 7.81 (d, 2H), 8.07-8.18 (2H), 8.25 (d,
2H), 8.45 (m, 2H), 10.52 (s, 1H).
(bb)
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (154)
(i)
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00339##
[1233] Carboxylic acid (149) (50 mg, 0.21 mmol) was coupled to
aniline (64) (42 mg, 0.21 mmol) using Method C. During this
reaction, partial hydrolysis occurred. The residue was re-dissolved
in EtOAc (2 ml) and the organic layer was washed with 1M HCl
(2.times.1 ml), dried (Na.sub.2SO.sub.4), filtered and the solvent
removed in vacuo to give a mixture of acid and ester, which was
used without further purification.
[1234] For the ester: LC/MS t.sub.r 1.76 min; MS(ES+) m/z 411, 413
(M+H).
(ii)
(3-{[6-(4-Chloro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (154)
##STR00340##
[1236] The mixture (86 mg, 0.21 mmol) was hydrolysed using Method
M. The residue was purified by column chromatography eluting with
47.5% EtOAc: 47.5% heptane: 5% AcOH to give the title compound.
[1237] Yield: 3 mg, 4% over 2 steps; LC/MS t.sub.r 1.55 Min;
MS(ES+) m/z 383, 385 (M+H); .sup.1H NMR (250 MHz; DMSO): .delta.
4.70 (s, 2H), 6.70 (d, 1H), 7.30 (t, 1H), 7.50 (d, 1H), 7.60 (m,
3H), 8.10-8.35 (m, 3H), 8.45 (d, 2H).
(cc)
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryli-
c acid (155)
(i)
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acrylic
acid ethyl ester
##STR00341##
[1239] Carboxylic acid (152) (50 mg, 0.23 mmol) was coupled to
aniline (60) (44 mg, 0.23 mmol) using Method C. The crude residue
was purified by column chromatography eluting with 10% EtOAc in
heptane to give the title compound.
[1240] Yield: 78 mg, 871; LC/MS t.sub.r 1.79 min; MS(ES+) m/z 391
(M+H).
(ii)
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-acryli-
c acid (155)
##STR00342##
[1242] The ester (65 mg, 0.17 mmol) was hydrolysed using Method M
to give the title compound.
[1243] Yield: 54 mg, 88%; LC/MS t.sub.r 1.53 min; MS(ES+) m/z 363
(M+H); HPLC Purity: 99%; .sup.1H NMR (250 MHz; DMSO): .delta. 6.44
(d, 1H), 7.13 (d, 1H), 7.26 (d, 1H), 7.40 (m, 3H), 7.86 (d, 1H),
8.01 (s, 1H), 8.08-8.30 (m, 3H), 8.47 (m, 2H), 10.55 (s, 1H).
(dd)
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (156)
(i)
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00343##
[1245] Carboxylic acid (145) (57 mg, 0.26 mmol) was coupled to
aniline (64) (50 mg, 0.26 mmol) using Method C to give the title
compound.
[1246] Yield: 61 mg, 59%; LC/MS t.sub.r 1.64 min; MS(ES+) m/z 400,
402 (M+H).
(ii)
(3-{[5-(4-Chloro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (156)
##STR00344##
[1248] The ester (61 mg, 0.15 mmol) was hydrolysed using Method M
to give the title compound.
[1249] Yield: 42 mg, 75%; LC/MS t.sub.r 1.50 min; MS(ES+) m/z 372,
374 (M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta.
4.14 (s, 2H), 6.57-6.60 (m, 1H), 7.17-7.24 (m, 2H), 7.30-7.33 (m,
2H), 7.45 (d, 1H) 7.57-7.60 (m, 2H), 8.01-8.03 (m, 2H), 10.25 (s,
1H).
(ee)
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (157)
(i)
(3-{[5-(4-fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00345##
[1251] Carboxylic acid (76) (53 mg, 0.26 mmol) was coupled to
aniline (64) (56 mg, 0.26 mmol) using Method C to give the title
compound.
[1252] Yield: 40 mg, 40%; LC/MS t.sub.r 1.54 min; MS(ES+) m/z 384
(M+H).
(ii)
(3-{[5-(4-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (157)
##STR00346##
[1254] The ester (40 mg, 0.10 mmol) was hydrolysed using Method M
to give the title compound.
[1255] Yield: 20 mg, 54%; LC/MS t.sub.r 1.44 min; MS(ES+) m/z 356
(M+H); HPLC Purity: 98%; .sup.1H NMR (250 MHz, DMSO) .delta. 4.68
(s, 2H), 6.67-6.71 (m, 1H), 7.14-7.45 (m, 7H), 8.01-8.05 (m,
2H).
(ff)
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (158)
(i)
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00347##
[1257] Carboxylic acid (152) (50 mg, 0.23 mmol) was coupled to
aniline (64) (45 mg, 0.23 mmol) using Method C to give the title
compound.
[1258] Yield: 35 mg, 39%; LC/MS t.sub.r 1.67 min; MS(ES+) m/z 395
(M+H).
(ii)
(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (158)
##STR00348##
[1260] The ester (35 mg, 0.09 mmol) was hydrolysed using Method M
to give the title compound.
[1261] Yield: 17 mg, 52%; LC/MS t.sub.r 1.45 min; MS(ES+) m/z 367
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta. 4.71
(s, 2H), 6.72-6.75 (m, 1H), 7.30-7.42 (m, 3H), 7.52-7.54 (m, 1H),
7.62 (s, 1H), 8.10-8.18 (m, 2H), 8.25-8.27 (m, 1H), 8.44-8.48 (m,
2H), 10.52 (s, 1H), 13.06 (s, 1H).
(gg)
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]amino}-phenyl)-propion-
ic acid (159)
(i)
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]amino}-phenyl)-propioni-
c acid ethyl ester
##STR00349##
[1263] Carboxylic acid (152) (50 mg, 0.23 mmol) was coupled to
aniline (124) (45 mg, 0.23 mmol) using Method C. The residue was
purified by column chromatography eluting with 30% EtOAc in heptane
to give the title compound.
[1264] Yield: 11 mg, 12%; LC/MS t.sub.r 1.77 min; MS(ES+) m/z 393
(M+H).
(j)
3-(3-{[6-(4-Fluoro-phenyl)-pyridine-2-carbonyl]amino}-phenyl)-propioni-
c acid (159)
##STR00350##
[1266] The ester (11 mg, 0.028 mmol) was hydrolysed using Method M
to give the title compound.
[1267] Yield: 5 mg, 49%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 365
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta. 2.59
(t, 2H), 2.88 (t, 2H), 7.05 (d, 1H), 7.31-7.43 (m, 3H), 7.76-7.80
(m, 2H), 8.10-8.18 (m, 2H), 8.25-8.27 (m, 1H), 8.45-8.48 (m, 2H),
10.49 (s, 1H), 12.19 (s, 1H).
(hh) {3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenoxy}-acetic acid
(160)
(i) {3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenoxy}-acetic acid
ethyl ester
##STR00351##
[1269] Carboxylic acid (56) (50 mg, 0.27 mmol) was coupled to
aniline (64) (52 mg, 0.27 mmol) using Method C. During this
reaction, partial hydrolysis occurred. The residue was re-dissolved
in EtOAc (2 ml) and the organic layer was washed with 1M HCl
(2.times.1 ml), dried (Na.sub.2SO.sub.4), filtered and the solvent
removed in vacuo to give a mixture of acid and ester, which was
used without further purification.
[1270] For the ester: LC/MS t.sub.r 1.47 min; MS(ES+) m/z 352
(M+H).
(ii) {3-[(5-Phenyl-furan-2-carbonyl)-amino]-phenoxy}-acetic acid
(160)
##STR00352##
[1272] The mixture (95 mg, 0.27 mmol) was hydrolysed using Method
M. The solid was recrystallised from a hot 10% EtOH in H.sub.2O
mixture and triturated with DCM (2 ml) to give the title
compound.
[1273] Yield: 20 mg, 22% over 2 steps; LC/MS t.sub.r 1.35 min;
MS(ES+) m/z 338 (M+H); HPLC Purity: 93%; .sup.1H NMR (400 MHz,
DMSO) .delta. 4.70 (s, 2H), 6.69-6.72 (m, 1H), 7.21-7.31 (m, 2H),
7.41-7.55 (m, 6H), 7.99-8.01 (m, 2H), 10.18 (s, 1H), 13.10 (s,
1H).
(ii)
3-(3-{[6-(3-Fluoro-Phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-propio-
nic acid (162)
(i) 3-{3-[(6-Bromo-pyridine-2-carbonyl)-amino]-phenyl}-propionic
acid ethyl ester (161)
##STR00353##
[1275] 6-Bromo-pyridine-2-carboxylic acid (261 mg, 1.29 mmol) was
coupled to aniline (124) (250 mg, 1.29 mmol) using Method C to give
the title compound.
[1276] Yield: 308 mg, 63%; LC/MS t.sub.r 1.58 min; MS(ES+) m/z 377,
379 (M+H).
(ii)
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-propio-
nic acid ethyl ester
##STR00354##
[1278] The pyridyl bromide (161) (100 mg, 0.27 mmol) was coupled to
3-fluoro-phenylboronic acid (34 mg, 0.24 mmol) using Method E. The
residue was purified by column chromatography eluting with 15%
EtOAc in heptane to give the title compound.
[1279] Yield: 75 mg, 80%; LC-MS t.sub.r 1.72 min; MS(ES+) m/z 393
(M+H).
(iii)
3-(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenyl)-propi-
onic acid (162)
##STR00355##
[1281] The ester (75 mg, 0.19 mmol) was hydrolysed using Method M
to give the title compound.
[1282] Yield: 60 mg, 87%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 365
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta. 2.59
(t, 2H), 2.88 (t, 2H), 7.06 (d, 1H), 7.31-7.39 (m, 2H), 7.59-7.64
(m, 1H), 7.76-7.80 (m, 2H), 8.14-8.19 (m, 3H), 8.30-8.36 (m, 2H),
10.52 (s, 1H), 12.21 (s, 1H).
(jj)
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid (163)
(i) 3-{3-[(5-Bromo-furan-2-carbonyl)-amino]-phenyl}-propionic acid
ethyl ester
##STR00356##
[1284] 5-Bromo-2-furoic acid (247 mg, 1.29 mmol) was coupled to
aniline (124) (250 mg, 1.29 mmol) using Method C to give the title
compound.
[1285] Yield: 247 mg, 52%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 366,
368 (M+H).
(ii)
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propionic
acid ethyl ester
##STR00357##
[1287] The furyl bromide (100 mg, 0.27 mmol) was coupled to
3-fluoro-phenylboronic (35 mg, 0.25 mmol) acid using Method E. The
residue Was purified by column chromatography eluting with 15%
EtOAc in heptane to give the title compound.
[1288] Yield: 77 mg, 81%; LC-MS t.sub.r 1.62 min; MS(ES+) m/z 382
(M+H).
(iii)
3-(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenyl)-propioni-
c acid (163)
##STR00358##
[1290] The ester (77 mg, 0.20 mmol) was hydrolysed using Method M
to give the title compound.
[1291] Yield: 67 mg, 95%; LC/MS t.sub.r 1.41 min; MS(ES+) m/z 354
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta. 2.58
(t, 2H), 2.86 (t, 2H), 7.02 (d, 1H), 7.23-7.32 (m, 3H), 7.41 (d,
1H), 7.53-7.66 (m, 3H), 7.84 (d, 1H), 7.91-7.95 (m, 1H), 10.52 (s,
1H), 12.21 (s, 1H).
(kk) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic
acid (164)
(i) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic
acid ethyl ester
##STR00359##
[1293] The pyridyl bromide (161) (100 mg, 0.27 mmol) was coupled to
phenylboronic acid (30 mg, 0.25 mmol) using Method E. The residue
was purified by column chromatography eluting with 15% EtOAc in
heptane to give the title compound.
[1294] Yield: 55 mg, 59%; LC-MS t.sub.r 1.73 min; MS(ES+) m/z 375
(M+H).
(ii) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic
acid (164)
##STR00360##
[1296] The ester (55 mg, 0.15 mmol) was hydrolysed using Method M
to give the title compound.
[1297] Yield: 16 mg, 31%; LC/MS t.sub.r 1.46 min; MS(ES+) m/z 347
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta. 2.59
(t, 2H), 2.88 (t, 2H), 7.05 (d, 1H), 7.31-7.35 (m, 1H), 7.51-7.61
(m, 3H), 7.77-7.80 (m, 2H), 8.11-8.18 (m, 2H), 8.25-8.28 (m, 1H),
8.37-8.39 (m, 2H), 10.48 (s, 1H), 12.19 (s, 1H).
(ll) 3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid
(165)
(i) 3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid
ethyl ester
##STR00361##
[1299] The phenyl bromide (139) (100 mg, 0.25 mmol) was coupled to
phenylboronic acid (28 mg, 0.23 mmol) using Method E. During this
reaction, partial hydrolysis occurred. The residue was extracted
using Work-up E1 to give a mixture of acid and ester, which was
used without further purification.
[1300] For the ester: LC/MS t.sub.r 1.61 min; MS(ES+) m/z 394
(M+H).
(ii) 3-[(4-Fluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid
(165)
##STR00362##
[1302] The mixture (90 mg, 0.23 mmol) was hydrolysed using Method
M. The residue was triturated with TBME (2 ml) to give the title
compound.
[1303] Yield: 41 mg, 49% over 2 steps; LC/MS t.sub.r 1.51 min;
MS(ES+) m/z 366 (M+H); HPLC Purity: 92%; .sup.1H NMR (250 MHz,
DMSO) .delta. 4.66 (s, 2H), 6.66-6.71 (d, 1H), 7.23-7.53 (m, 7H),
7.73-7.76 (m, 2H), 7.85-7.93 (m, 2H), 10.52 (s, 1H).
(mm) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic
acid (167)
(i) {3-[(6-Bromo-pyridine-2-carbonyl)-amino]-phenoxy}-acetic acid
ethyl ester (166)
##STR00363##
[1305] 6-Bromo-pyridine-2-carboxylic acid (250 mg, 1.24 mmol) was
coupled to aniline (64) (241 mg, 1.24 mmol) using Method C to give
the title compound.
[1306] Yield: 387 mg, 82%; LC/MS t.sub.r 1.49 min; MS(ES+) m/z 379,
381 (M+H).
(ii) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-propionic
acid (167)
##STR00364##
[1308] Bromo-derivative (166) (100 mg, 0.26 mmol) was coupled to
phenylboronic (30 mg, 0.25 mmol) acid using Method E. During this
reaction, hydrolysis occurred. The residue was extracted using
Work-up E1 and triturated with TBME (2 ml) to give the title
compound.
[1309] Yield: 48 mg, 55%; LC/MS t.sub.r 1.42 min; MS(ES+) m/z 349
(M+H); HPLC Purity: 100%; .sup.1H NMR (400 MHz, DMSO) .delta. 4.71
(s, 2H), 6.72-6.75 (m, 1H), 7.29-7.34 (m, 1H), 7.52-7.63 (m, 5H),
8.10-8.18 (m, 2H), 8.25-8.28 (m, 1H), 8.36-8.38 (m, 2H), 10.51 (s,
1H), 13.07 (s, 1H).
(nn)
(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (168)
(i) {3-[(5-Bromo-furan-2-carbonyl)-amino]-phenoxy}-acetic acid
ethyl ester
##STR00365##
[1311] 5-Bromo-furan-2-carboxylic acid (245 mg, 1.28 mmol) was
coupled to aniline (64) (250 mg, 1.28 mmol) using Method C. The
residue was purified by column chromatography eluting with 15%
EtOAc in heptane to give the title compound.
[1312] Yield: 360 mg, 76%; LC/MS t.sub.r 1.41 min; MS(ES+) m/z 368,
370 (M+H).
(ii)
(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00366##
[1314] The furyl bromide (100 mg, 0.27 mmol) was coupled to
3-fluoro-phenylboronic acid (35 mg, 0.25 mmol) using Method E.
During this reaction, partial hydrolysis occurred. The residue was
extracted using Work-up E1 to give a mixture of acid and ester,
which was used without further purification.
[1315] For the ester: LC/MS t.sub.r 1.57 min; MS(ES+) m/z 384
(M+H).
(iii)
(3-{[5-(3-Fluoro-phenyl)-furan-2-carbonyl]-amino}-phenoxy)-acetic
acid (168)
##STR00367##
[1317] The mixture (95 mg, 0.25 mmol) was hydrolysed using Method
M. The residue was triturated with TBME (2 ml) to give the title
compound. Yield: 71 mg, 80% over 2 steps; LC/MS t.sub.r 1.43 min;
MS(ES+) m/z 356 (M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz,
DMSO): .delta. 4.69 (s, 2H), 6.70 (d, 1H), 7.19-7.33 (m, 3H),
7.36-7.47 (m, 3H), 7.51-7.61 (m, 1H), 7.81-7.96 (m, 2H), 10.20 (s,
1H).
(oo) {3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (169)
(i) {3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid ethyl ester
##STR00368##
[1319] The phenyl bromide (139) (100 mg, 0.25 mmol) was coupled to
3-fluoro-phenylboronic acid (34 mg, 0.24 mmol) using Method E.
During this reaction, partial hydrolysis occurred. The residue was
extracted using Work-up E1 to give a mixture of acid and ester,
which was used without further purification.
[1320] For the ester: LC/MS t.sub.r 1.62 min; MS(ES+) m/z 412
(M+H).
(ii) {3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (169)
##STR00369##
[1322] The mixture (99 mg, 0.24 mmol) was hydrolysed using Method
M. The residue was triturated with TBME (2 ml) to give the title
compound. Yield: 30 mg, 33% over 2 steps; LC/MS t.sub.r 1.54 min;
MS(ES+) m/z 384 (M+H); HPLC Purity: 100%; .sup.1H NMR (250 MHz,
DMSO): .delta. 4.47 (s, 2H), 6.64 (d, 1H), 7.19-7.29 (m, 2H),
7.31-7.39 (m, 2H), 7.41-7.67 (m, 4H), 7.88-8.01 (m, 2H), 10.49 (s,
1H).
(pp)
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (170)
(i)
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid ethyl ester
##STR00370##
[1324] The pyridyl bromide (166) (100 mg, 0.26 mmol) was coupled to
3-fluoro-phenylboronic acid (34 mg, 0.24 mmol) using Method E.
During this reaction, partial hydrolysis occurred. The residue was
extracted using Work-up E1 to give a mixture of acid and ester,
which was used without further purification.
[1325] For the ester: LC/MS t.sub.r 1.43 min; MS(ES+) m/z 395
(M+H).
(ii)
(3-{[6-(3-Fluoro-phenyl)-pyridine-2-carbonyl]-amino}-phenoxy)-acetic
acid (170)
##STR00371##
[1327] The mixture (94 mg, 0.24 mmol) was hydrolysed using Method
M. The residue was triturated with TBME (2 ml) to give the title
compound. Yield: 88 mg, 100% over 2 steps; LC/MS t.sub.r 1.43 min;
MS(ES+) m/z 367 (M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz,
DMSO): .delta. 4.49 (s, 2H), 6.51 (d, 1H), 7.06-7.18 (m, 2H),
7.27-7.46 (m, 3H), 7.89-7.99 (m, 3H), 8.04-8.12 (m, 2H), 10.32 (s,
1H).
(qq) {3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (171)
(i) {3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid ethyl ester
##STR00372##
[1329] The phenyl bromide (139) (100 mg, 0.25 mmol) was coupled to
4-fluoro-phenylboronic acid (33 mg, 0.23 mmol) using Method E.
During this reaction, partial hydrolysis occurred. The residue was
extracted using Work-up E1 to give a mixture of acid and ester,
which was used without further purification.
[1330] For the ester: LC/MS t.sub.r 1.62 min; MS(ES+) m/z 412
(M+H).
(ii) {3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic
acid (171)
##STR00373##
[1332] The mixture (95 mg, 0.23 mmol) was hydrolysed using Method
M. The residue was triturated with TBME (2 ml) to give the title
compound. Yield: 32 mg, 36% over 2 steps; LC/MS t.sub.r 1.53 min;
MS(ES+) m/z 384 (M+H); HPLC Purity: 97%; .sup.1H NMR (250 MHz,
DMSO): .delta. 4.67 (s, 2H), 6.69 (d, 7.21-7.50 (m, 6H), 7.74-7.93
(m, 4H), 10.51 (s, 1H).
(rr) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acrylic
acid (178)
(i) 3-{3-[(6-Bromo-pyridine-2-carbonyl)-amino]-phenyl}-acrylic acid
ethyl ester
##STR00374##
[1334] Aniline (60) (124 mg, 0.6 mmol) was coupled to
6-bromo-pyridine-2-carboxylic acid (131 mg, 0.6 mmol) using Method
C. The residue was purified by column chromatography eluting in 10%
EtOAc in heptane to give the title compound.
[1335] Yield: 25 mg, 11%; LC/MS t.sub.r 1.61 min; MS(ES+) m/z 375,
377 (M+).
(ii) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acrylic
acid ethyl ester
##STR00375##
[1337] The pyridyl bromide (25 mg, 0.06 mmol) was coupled to
benzeneboronic acid (7 mg, 0.05 mmol) using Method E. The residue
was purified by column chromatography eluting in 10% EtOAc in
heptane.
[1338] Yield: 5 mg, 22%; LC/MS t.sub.r 1.79 min; MS(ES+) m/z 373
(M+H).
(iii) 3-{3-[(6-Phenyl-pyridine-2-carbonyl)-amino]-phenyl}-acrylic
acid (178)
##STR00376##
[1340] The ester (5 mg, 0.001 mmol) was hydrolysed using Method G
to give the title compound.
[1341] Yield: 5 mg, 100%; LC/MS t.sub.r 1.50 min; MS(ES+) m/z 345
(M+H); HPLC Purity: 98%; .sup.1H NMR (400 MHz; DMSO): .delta. 6.55
(d, 1H), 7.43-7.65 (m, 6H), 8.03 (m, 1H), 8.15 (m, 3H), 8.27 (d,
1H), 8.38 (d, 2H), 10.59 (s, 1H).
Example 11
(a) 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide (173)
(i) N-(3-Cyanomethoxy-phenyl)-acetamide
##STR00377##
[1343] To a solution of N-(3-hydroxy-phenyl)-acetamide (5 g, 33.1
mmol) in acetone (50 ml) were added K.sub.2CO.sub.3 (5.49 g, 39.8
mmol) and bromo-acetonitrile (4.37 g, 36.4 mmol). The reaction
mixture was heated to 100.degree. C. for 3 h, filtered and the
acetone layer evaporated in vacuo. This residue was dissolved in
EtOAc (100 ml) and washed with 1M NaOH (10 ml.times.2). The organic
layer was dried (Na.sub.2SO.sub.4), filtered and the solvent
removed in vacuo. The crude residue was purified by column
chromatography eluting with 80% EtOAc in heptane to give the title
compound.
[1344] Yield: 6.25 g, 99%; LC/MS t.sub.r 0.92 min; MS(ES+) m/z 191
(M+H).
(ii) (3-Amino-phenoxy)-acetonitrile (172)
##STR00378##
[1346] The acetamide (2 g, 10.5 mmol) was suspended in 1M HCl and
heated to 100.degree. C. for 4.5 h. The solution was allowed to
cool to room temperature overnight, then the water was removed in
vacuo to give the title compound as the hydrochloride salt.
[1347] Yield: 1.5 g, 97%; LC/MS t.sub.r 0.66 min; MS(ES+) m/z 149
(M+H).
(iii) 5-Bromo-furan-2-carboxylic acid
(3-cyanomethoxy-phenyl)-amide
##STR00379##
[1349] 5-Bromo-furan-2-carboxylic acid (325 mg, 1.70 mmol) was
coupled to (3-amino-phenoxy)-acetonitrile (172) (250 mg, 1.69 mmol)
using Method C. The residue was purified by column chromatography
eluting with a stepped gradient of 10-30% EtOAc in heptane to give
the title compound. Yield: 90 mg, 16%; LC/MS t.sub.r 1.34 min;
MS(ES+) m/z 321, 323 (M+H).
(iv) 5-Bromo-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide
##STR00380##
[1351] The nitrile (100 mg, 0.31 mmol) was treated with TMSN.sub.2
and Bu.sub.2SnO using Method L, except the reaction mixture was
diluted with EtOAc (2 ml) and washed with H.sub.2O (2.times.2 ml).
The organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo to give the title compound. Yield: 110 mg,
97%; LC/MS t.sub.r 1.17 min; MS(ES+) m/z 364, 366 (M+H).
(v) 5-Phenyl-furan-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide (173)
##STR00381##
[1353] The bromo-derivative (110 mg, 0.30 mmol) was coupled to
phenylboronic acid (37 mg, 0.30 mmol) acid using Method E, except
for heating to 80.degree. C. for 20 min. After reaction, 1M HCl (3
ml) was added, and the solvents were removed in vacuo. The residue
was triturated with TBME (2 ml), DCM (2 ml), and recrystallised
from hot 10% EtOH in H.sub.2O mixture to give the title
compound.
[1354] Yield: 62 mg, 57%; LC/MS t.sub.r 1.95 min; MS(ES+) m/z 362
(M+H); HPLC Purity: 95%; .sup.1H NMR (400 MHz, DMSO): .delta. 5.34
(8, 2H), 6.69 (d, 1H), 7.03 (d, 1H), 7.17 (t, 1H), 7.22-7.29 (m,
3H), 7.36 (t, 2H), 7.42 (s, 1H), 7.82 (s, 2H), 10.03 (s, 1H).
(b) 6-Phenyl-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide (174)
(i) 6-Bromo-pyridine-2-carboxylic acid
(3-cyanomethoxy-phenyl)-amide
##STR00382##
[1356] 6-Bromo-pyridine-2-carboxylic acid (341 mg, 1.69 mmol) was
coupled to aniline (172) (250 mg, 1.69 mmol) using Method C. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[1357] Yield: 130 mg, 23%; LC/MS t.sub.r 1.43 min; MS(ES+) m/z 332,
334 (M+H).
(ii) 6-Bromo-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide
##STR00383##
[1359] The nitrile (130 mg, 0.39 mmol) was treated with TMSN.sub.3
and Bu.sub.2SnO using Method L, except the reaction mixture was
diluted with EtOAc (2 ml) and washed with H.sub.2O (2.times.2 ml).
The organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo. The residue was purified by column
chromatography eluting with 50% EtOAc in heptane followed by 5%
AcOH in EtOAc to give the title compound.
[1360] Yield: 100 mg, 68%; LC/MS t.sub.r 1.20 min; MS(ES+) m/z 375,
377 (M+H).
(iii) 6-Phenyl-pyridine-2-carboxylic acid
[3-(1H-tetrazol-5-ylmethoxy)-phenyl]-amide (174)
##STR00384##
[1362] The bromo-derivative (100 mg, 0.27 mmol) was coupled to
phenylboronic acid (27 mg, 0.22 mmol) acid using Method E, except
for heating to 80.degree. C. for 20 min. After reaction, 1M HCl (3
ml) was added, and the aqueous layer was extracted with EtOAc
(2.times.2 ml). The organic layer was dried (Na.sub.2SO.sub.4),
filtered and the solvent removed in vacuo. The residue was
triturated with TBME (2 ml) and DCM (2 ml) to give the title
compound. Yield: 82 mg, 100%; LC/MS t.sub.r 2.03 min; MS(ES+) m/z
373 (M+H); HPLC Purity: 93%; .sup.1H NMR (400 MHz, DMSO): .delta.
5.29 (s, 2H), 6.65 (d, 1H), 7.13 (t, 1H), 7.28-7.48 (m, 4H), 7.52
(s, 1H), 7.86-7.95 (m, 2H), 8.03 (d, 1H), 8.13 (d, 2H), 10.30 (s,
1H).
(c) 6-Phenyl-pyridine-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide (175)
(i) 6-Bromo-pyridine-2-carboxylic acid
[3-(2-cyano-vinyl)-phenyl]-amide
##STR00385##
[1364] 6-Bromo-pyridine-2-carboxylic acid (350 mg, 1.73 mmol) was
coupled to aniline (88) (250 mg, 1.74 mmol) using Method C. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[1365] Yield: 325 mg, 57%; LC/MS t.sub.r 1.52 min; MS(ES+) m/z 328,
330 (M+H).
(ii) 6-Bromo-pyridine-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide
##STR00386##
[1367] The nitrile (325 mg, 0.99 mmol) was reacted with TMSN.sub.3
and Bu.sub.2SnO using Method L, except the reaction mixture was
diluted with EtOAc (4 ml) and washed with H.sub.2O (3.times.4 ml).
The organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo. The residue was purified by column
chromatography eluting with 50% EtOAc in heptane followed by 5%
AcOH in EtOAc to give the title compound.
[1368] Yield: 334 mg, 25%; LC/MS t.sub.r 1.29 min; MS(ES+) m/z 371,
373 (M+H).
(iii) 6-Phenyl-pyridine-2-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide (175)
##STR00387##
[1370] The bromo-derivative (100 mg, 0.27 mmol) was coupled to
phenylboronic acid (27 mg, 0.22 mmol) using Method E, except that
the reaction was heated to 80.degree. C. After reaction, 1M HCl (3
ml) was added, and the aqueous layer was extracted with EtOAc
(2.times.2 ml). The organic layer was dried (Na.sub.2SO.sub.4),
filtered and the solvent removed in vacuo. The residue was
triturated with TBME (2 ml) and DCM (2 ml) to give the title
compound.
[1371] Yield: 54 mg, 67%; LC/MS t.sub.r 2.07 min; MS(ES+) m/z 369
(M+H); HPLC Purity: 92%; .sup.1H NMR (400 MHz, DMSO): .delta. 7.29
(d, 1H), 7.39-7.55 (m, 5H), 7.67 (d, 1H), 7.92 (d, 1H), 8.02-8.12
(m, 2H), 8.03-8.23 (m, 2H), 8.26-8.34 (m, 2H), 10.59 (s, 1H).
(d) 4-Fluoro-biphenyl-3-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide (176)
(i) 5-Bromo-N-[3-(2-cyano-vinyl)-phenyl]-2-fluoro-benzamide
##STR00388##
[1373] 5-Bromo-2-fluoro-benzoic acid (380 mg, 1.74 mmol) was
coupled to aniline (88) (250 mg, 1.74 mmol) using Method C. The
residue was purified by column chromatography eluting with 20%
EtOAc in heptane to give the title compound.
[1374] Yield: 353 mg, 59%; LC/MS t.sub.r 1.50 min; MS(ES+) m/z 345,
347 (M+H).
(ii)
5-Bromo-2-fluoro-N-{3-[2-(2H-tetrazol-5-yl)-vinyl]-phenyl}-benzamide
##STR00389##
[1376] The nitrile (353 mg, 1.02 mmol) was treated with TMSN.sub.3
and Bu.sub.2SnO using Method L, except the reaction mixture was
diluted with EtOAc (4 ml) and washed with H.sub.2O (3.times.4 ml).
The organic layer was dried (Na.sub.2SO.sub.4), filtered and the
solvent removed in vacuo. The residue was triturated with DCM (5
ml) to give the title compound.
[1377] Yield: 280 mg, 71%; LC/MS t.sub.r 1.32 min; MS(ES+) m/z 388,
390 (M+H).
(iii) 4-Fluoro-biphenyl-3-carboxylic acid
{3-[2-(1H-tetrazol-5-yl)-vinyl]phenyl}-amide (176)
##STR00390##
[1379] The phenyl bromide (100 mg, 0.27 mmol) was coupled to
phenylboronic acid (27 mg, 0.22 mmol) using Method E, except that
the reaction was heated at 80.degree. C. After reaction, 1M HCl (3
ml) was added, and the aqueous layer was extracted with EtOAc
(2.times.2 ml). The organic layer was dried (Na.sub.2SO.sub.4),
filtered and the solvent removed in vacuo. The residue was
triturated with TBME (2 ml) and DCM (2 ml) and further purified by
preparative HPLC to give the title compound.
[1380] Yield: 15 mg, 18%; LC/MS t.sub.r 2.04 min; MS(ES+) m/z 386
(M+H); HPLC Purity: 97%; .sup.1H NMR (400 MHz, DMSO): .delta. 7.39
(d, 1H), 7.49-7.69 (m, 6H), 7.76 (d, 1H), 7.83-7.90 (m, 3H),
7.98-8.03 (m, 1H), 8.08 (d, 1H), 8.22 (s, 1H), 10.72 (s, 1H).
Example 9
Biological Results
Binding Ability to Human EP Receptors
[1381] Membranes were prepared from cells stably transfected with
human EP receptor cDNA. In brief, cells were cultured to
confluency, scraped from culture flasks, and centrifuged (800 g, 8
minutes, 4.degree. C.). Cells were twice washed in ice cold
homogenisation buffer containing 10 mMTris-HCl, 1 mM EDTA.2Na, 250
mM sucrose, 1 mM PMSF, 0.3 mM indomethacin, pH 7.4, homogenised and
re-centrifuged as before. The supernatant was stored on ice and
pellets re-homogenised and re-spun. Supernatants were pooled and
centrifuged at 40000 g, 10 minutes, 4.degree. C. Resultant membrane
pellets were stored at -80.degree. C. until use.
[1382] For assay, membranes expressing human EP.sub.4, EP.sub.3,
EP.sub.2 or EP.sub.1 receptors were incubated in Millipore
(MHVBN45) plates containing assay buffer, radiolabelled
[.sup.3H]PGE.sub.2 and 0.1 to 10 000 nM concentrations of
compounds. Incubations were performed at suitable temperatures and
for suitable times to allow equilibrium to be reached. Non-specific
binding was determined in the presence of 10 uM PGE.sub.2. Bound
and free radiolabel was separated by vacuum manifold filtration
using appropriate wash buffers, and bound radiolabel was determined
by scintillation counting. Constituents of each of the buffers are
included in table 1 below.
[1383] The affinity or pK.sub.i of each compound for each receptor
was calculated from the concentration causing 50% radioligand
displacement (IC.sub.50) using the Cheng-Prusoff equation:
Ki = IC 50 1 + ( radioligand concentration radioligand KD )
##EQU00001##
[1384] This approach follows that set out in Kenakin, T. P.,
Pharmacologic analysis of drug receptor interaction. Raven Press,
New York, 2.sup.nd edition.
TABLE-US-00005 TABLE 1 Receptor EP.sub.1 EP.sub.2 EP.sub.3 EP.sub.4
Protein/well 6.5 .mu.g 8 .mu.g 5 .mu.g 5 .mu.g Final 3.6 nM 3 nM
2.5 nM 1 nM [.sup.3H-PGE.sub.2] Buffer Assay 10 mM MES pH 6.0; 10
mM MES 10 mM MES pH 10 mM MES 10 mM MgCl.sub.2; 1 mM pH 6.0; 10 mM
6.0; 10 mM pH 6.0; 10 mM EDTA, 3 uM MgCl.sub.2; 1 mM MgCl.sub.2; 1
mM MgCl.sub.2; 1 mM Indomethacin EDTA EDTA, 100 uM EDTA, 3 uM
GTP-gamma-S Indomethacin Wash 10 mM MES pH 6.0; 10 mM MES 10 mM MES
pH 10 mM MES 10 mM MgCl.sub.2 pH 6.0; 10 mM 6.0; 10 mM MgCl.sub.2
pH 6.0; 1 mM MgCl.sub.2 EDTA
Determination of Agonist Activity at Recombinant Human EP.sub.2
Prostanoid Receptors and Antagonist Activity at EP.sub.4 Prostanoid
Receptors
[1385] HEK-293 cell clones stably transfected with human EP.sub.2
or EP, prostanoid receptors were cultured at 37.degree. C. in a 5%
CO.sub.2 incubator, in 96-well poly-L-lysine coated plates at a
density of 50,000 cells/well. Culture media was Minimal essential
media (MEM), supplemented with 10% foetal bovine serum, 100 U/ml
penicillin, 100 ng/ml streptomycin, 2.5 .mu.g/ml fungizone, 2 mM
glutamine. Cells were cultured to confluency (3-4 days) prior to
use.
[1386] Culture media was removed, and confluent cells washed three
times in MEM. 175 .mu.l assay buffer (MEM containing no
supplements+1 mM IBMX) was incubated with the cells for 60 min.
Cells were then stimulated by the addition of 25 .mu.l of PGE.sub.2
or agonists prepared in assay buffer. In antagonist studies, cells
were pre-incubated with compounds for 30 minutes prior to
PGE.sub.2-mediated stimulation
[1387] Plates were incubated for 15 min at 37.degree. C., before
termination of the reaction by the addition of 25 .mu.l 1M HCl. The
plate was then frozen at -20.degree. C. overnight before
determination of cAMP concentration.
[1388] Stimulated cAMP levels were determined by radioligand
displacement binding. In brief, plates were thawed rapidly in a
waterbath, and the samples neutralised by the addition of 25 .mu.l
1M NaOH. 30 .mu.l was transferred to Millipore plates pre-coated
with 0.5% Polyethylenimine (PEI). Samples were diluted by addition
of 90 .mu.l cAMP determination buffer (50 mM Tris, 5 mM EDTA, pH
7.0). A cAMP standard curve (10.sup.-11M to 10.sup.-5M) was
constructed. 15 .mu.l of 2 nM (final concentration) [.sup.3H] cAMP,
and 15 .mu.l of 3'5'-cAMP protein kinase (8 .mu.g/well final
concentration) prepared in cAMP determination buffer containing
0.1% BSA, were added to each well.
[1389] Plates were incubated on ice for 2 hours, before bound and
free radiolabel were separated by vacuum filtration harvesting
using the Millipore vacuum manifold, using ice cold water as the
termination buffer.
[1390] The sealing mat was removed from the Millipore plates, and
the filters allowed to dry overnight. 50 .mu.l Microscint 0
(Packard Bioscience) was added to each well, and the plate counted
using the Micro-Beta Trilux topcount .sup.3H program.
[1391] cAMP accumulation was determined from the standard curve,
and values calculated in pmoles cAMP/well. Antagonists affinities
(pA.sub.2 values) were determined assuming a elope of unity and the
Gaddam-Schild equation, where pA.sub.2=log [concentration
ratio-1]-log [antagonist]. Agonist potencies were determined from
log EC.sub.50 values, denoting the concentration of agonist
required to produce 50% of the agonist response.
[1392] Binding and functional results are presented as pK.sub.i and
pEC.sub.50/pA.sub.2 values in table 2 below.
TABLE-US-00006 TABLE 2 pKi (M) pEC.sub.50 EP.sub.2 pA.sub.2
Compound EP.sub.2 EP.sub.4 EP.sub.3 (M) EP.sub.4 (M) activity 2
>5 >5 -- >5 >5 EP.sub.2 agonist/EP.sub.4 antagonist 4
>5 >5 -- >5 >5 EP.sub.2 agonist/EP.sub.4 antagonist 10
>6 -- -- >6 EP.sub.2 agonist 12 >6 -- -- >6 EP.sub.2
agonist 14 >6 -- -- >5 EP.sub.2 agonist 16 >5 -- -- >5
EP.sub.2 agonist 17 >6 -- -- >6 EP.sub.2 agonist 18 >6 --
-- >6 EP.sub.2 agonist 19 >6 -- -- >5 EP.sub.2 agonist 20
>6 -- -- >5 EP.sub.2 agonist 21 >6 -- -- >6 EP.sub.2
agonist 22 >5 -- -- 23 >5 -- -- 24 >6 -- -- 25 >5 -- --
26 >7 >7 -- >7 >6 EP.sub.2 agonist/EP.sub.4 antagonist
27 >7 -- -- >7 EP.sub.2 agonist 28 >6 -- -- 29 >6 -- --
30 >5 -- -- >6 EP.sub.2 Agonist 31 >6 >6 -- >6
EP.sub.2 agonist 32 >6 >5 -- 33 >5 -- -- 34 >6 >6 --
>6 EP.sub.2 agonist 35 >5 -- -- 36 >6 -- -- >7 EP.sub.2
agonist 37 >6 -- -- >6 EP.sub.2 agonist 38 >5 -- -- 39
>7 -- -- >7 EP.sub.2 agonist 40 >6 -- -- >7 EP.sub.2
agonist 41 >6 -- -- >6 EP.sub.2 agonist 42 >6 -- -- >7
EP.sub.2 agonist 43 >5 -- -- 44 >6 -- -- >7 EP.sub.2
agonist 45 >6 -- -- >7 EP.sub.2 agonist 46 >5 -- -- 47
>6 -- -- 48 >5 -- -- 49 >6 -- -- >7 EP.sub.2 agonist 50
>5 -- -- 51 >6 -- -- >7 EP.sub.2 agonist 52 >6 -- --
>7 EP.sub.2 agonist 53 >5 -- -- 54 >6 -- -- >6 EP.sub.2
agonist 57 >5 -- -- >6 EP.sub.2 Agonist 59 >5 -- -- 61
>7 >6 -- >7 >6 EP.sub.2 agonist/EP.sub.4 agonist 62
>6 -- -- >7 EP.sub.2 agonist 63 >5 -- -- 66 >7 >6 --
>7 >6 EP.sub.2 agonist/EP.sub.4 agonist 68 >7 >6 --
>7 >6 EP.sub.2 agonist/EP.sub.4 antagonist 69 >7 >6 --
EP.sub.2 agonist/EP.sub.4 antagonist 70 >7 >6 -- EP.sub.2
agonist/EP.sub.4 antagonist 71 >7 -- -- EP.sub.2 agonist 72
>6 >5 -- >6 >6 EP.sub.2 agonist/EP.sub.4 antagonist 73
>5 -- -- 74 >5 -- -- >5 EP.sub.2 agonist 75 >7 -- -- 81
>7 -- -- >7 EP.sub.2 Agonist 82 >7 -- -- >7 EP.sub.2
Agonist 85 >7 -- -- >7 EP.sub.2 Agonist 86 >7 -- >7
EP.sub.2 Agonist 87 >7 -- -- >7 EP.sub.2 Agonist 89 >7 --
-- >7 EP.sub.2 Agonist 90 >7 -- -- >7 EP.sub.2 Agonist 92
>6 -- -- >7 EP.sub.2 Agonist 93 >7 -- -- >7 EP.sub.2
Agonist 94 >7 -- -- >7 EP.sub.2 Agonist 95 >7 -- -- >7
EP.sub.2 Agonist 96 >6 -- -- 97 >6 -- -- >6 EP.sub.2
Agonist 98 >6 -- -- >6 EP.sub.2 Agonist 100 >7 >5 --
>7 EP.sub.2 Agonist 101 >7 -- -- >7 EP.sub.2 Agonist 102
>7 -- -- 103 >7 >6 -- 104 >7 -- -- 105 >6 -- -- 107
>7 -- -- >7 EP.sub.2 Agonist 108 >7 -- -- >7 EP.sub.2
Agonist 110 >7 -- -- >7 EP.sub.2 Agonist 111 >7 -- --
>7 EP.sub.2 Agonist 112 >7 -- -- >7 EP.sub.2 Agonist 113
>7 -- -- >7 EP.sub.2 Agonist 115 >7 -- -- >7 EP.sub.2
Agonist 116 >7 -- -- >7 EP.sub.2 Agonist 117 >6 -- --
>5 EP.sub.2 Agonist 118 >6 -- -- >7 EP.sub.2 Agonist 120
>5 -- -- >6 EP.sub.2 Agonist 121 >6 -- -- >6 EP.sub.2
Agonist 122 >7 >6 -- 123 >6 -- -- 125 >7 >5 -- >7
>5 EP.sub.2 Agonist/EP.sub.4 Antagonist 126 >7 >6 -- >7
>6 EP.sub.2 Agonist/EP.sub.4 Antagonist 127 >7 -- -- >7
EP.sub.2 Agonist 128 >6 -- -- >7 EP.sub.2 Agonist 129 >7
>6 -- >7 >6 EP.sub.2 Agonist/EP.sub.4 Antagonist 130 >7
>6 -- >7 >6 EP.sub.2 Agonist/EP.sub.4 Antagonist 132 >7
-- -- >7 EP.sub.2 Agonist 133 >7 >6 -- >7 >7
EP.sub.2 Agonist/EP.sub.4 Agonist 134 >7 -- -- >7 EP.sub.2
Agonist 135 >6 -- -- >6 EP.sub.2 Agonist 137 >7 >6 --
>7 EP.sub.2 Agonist 138 >7 >7 -- >7 >6 EP.sub.2
Agonist/EP.sub.4 Agonist 140 >7 -- -- >7 EP.sub.2 Agonist 142
>7 -- -- >7 EP.sub.2 Agonist 143 >7 -- -- >7 EP.sub.2
Agonist 144 >7 >6 -- >7 >6 EP.sub.2 Agonist 146 >7
-- -- >7 EP.sub.2 Agonist 147 >7 -- -- >7 EP.sub.2 Agonist
148 >7 -- -- >7 EP.sub.2 Agonist 150 >6 -- -- >6
EP.sub.2 Agonist 151 >7 -- -- >7 EP.sub.2 Agonist 153 >7
-- -- >7 EP.sub.2 Agonist 154 >7 -- -- >7 EP.sub.2 Agonist
155 >7 -- -- >7 EP.sub.2 Agonist 156 >7 -- -- >7
EP.sub.2 Agonist 157 >7 -- -- >7 EP.sub.2 Agonist 158 >7
>6 -- >7 EP.sub.2 Agonist 159 >7 -- -- >7 EP.sub.2
Agonist 160 >7 -- -- >7 EP.sub.2 Agonist 162 >7 -- --
>7 EP.sub.2 Agonist 163 >7 -- -- >7 EP.sub.2 Agonist 164
>6 -- -- >7 EP.sub.2 Agonist 165 >7 -- -- >7 EP.sub.2
Agonist 167 >7 >6 -- >7 EP.sub.2 Agonist 168 >7 -- --
>7 EP.sub.2 Agonist 169 >7 -- -- >7 EP.sub.2 Agonist 170
>7 >6 -- >7 EP.sub.2 Agonist 171 >7 -- -- >7
EP.sub.2 Agonist 173 >6 -- -- >7 EP.sub.2 Agonist 174 >7
>6 -- 175 >7 >7 -- 176 >7 -- -- 177 >6 -- -- >6
EP.sub.2 Agonist 178 >7 >7 -- >7 >6 EP.sub.2
Agonist/EP.sub.4 Agonist -- denotes no appreciable affinity up to
10 .mu.M.
* * * * *