IP Library › Granted Patent US 7,456,204

Granted Patent B2

US 7,456,204 · App. 10/560,771 · Granted Nov 25, 2008

Cyclohexylglycine derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes

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Quick Facts

Patent No.: US 7,456,204
App. No.: 10/560,771
Granted: Nov 25, 2008
Kind: B2

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Abstract

The present invention is directed to novel cyclohexylglycine derivatives which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.

Claims (68)

1. A compound of structural formula I:

wherein:

each n is independently 0, 1, 2, or 3;

W is selected from the group consisting of CH 2 , CHF, and CF 2 ;

X is selected from the group consisting of S, S(O), S(O) 2 , CH 2 , CHF, and CF 2 ;

Y and Z are each independently selected from the group consisting of O, S, N, and NR 7 , with the proviso that at least one of Y and Z is N;

R 1 is hydrogen or cyano;

R 2 is selected from the group consisting of

hydrogen,

halogen,

cyano,

hydroxy,

C 1-6 alkyl, wherein alkyl is unsubstituted or substituted with one to five halogens,

C 1-6 alkoxy, wherein alkoxy is unsubstituted or substituted with one to five halogens,

(CH 2 ) n —COOH,

(CH 2 ) n —COOC 1-6 alkyl,

(CH 2 ) n —CONR 3 R 4 ,

(CH 2 ) n —NR 3 R 4 ,

(CH 2 ) n —NR 6 SO 2 R 5 ,

(CH 2 ) n —NR 6 CONR 3 R 4 ,

(CH 2 ) n —NR 6 COR 6 ,

(CH 2 ) n —NR 6 CO 2 R 5 ,

(CH 2 ) n -aryl, wherein aryl is unsubstituted or substituted with one to five substituents independently selected from halogen, hydroxy, CO 2 H, C 1-6 alkyloxycarbonyl, C 1-6 alkyl, C 3-6 cycloalkyl, and C 1-6 alkoxy, wherein alkyl and alkoxy are unsubstituted or substituted with one to five halogens,

wherein any methylene (CH 2 ) carbon atom in R 2 is independently unsubstituted or substituted with one to two groups independently selected from halogen, hydroxy, and

C 1-4 alkyl unsubstituted or substituted with one to five halogens;

R 3 and R 4 are independently selected from the group consisting of

hydrogen,

(CH 2 ) n -phenyl,

(CH 2 ) n —C 3-6 cycloalkyl, and

C 1-6 alkyl,

wherein alkyl is unsubstituted or substituted with one to five halogens and wherein phenyl and cycloalkyl are unsubstituted or substituted with one to five substituents independently selected from halogen, hydroxy, C 1-6 alkyl, and C 1-6 alkoxy, wherein alkyl and alkoxy are unsubstituted or substituted with one to five halogens; or

R 3 and R 4 together with the nitrogen atom to which they are attached form a heterocyclic ring selected from azetidine, pyrrolidine, piperidine, piperazine, and morpholine wherein said heterocyclic ring is unsubstituted or substituted with one to three substituents independently selected from halogen, hydroxy, C 1-6 alkyl, and

C 1-6 alkoxy, wherein alkyl and alkoxy are unsubstituted or substituted with one to five halogens;

each R 5 is independently selected from the group consisting of (CH 2 ) n -phenyl, (CH 2 ) n —C 3-6 cycloalkyl, and C 1-6 alkyl, wherein alkyl is unsubstituted or substituted with one to five halogens and wherein phenyl and cycloalkyl are unsubstituted or substituted with one to five substituents independently selected from halogen, hydroxy, C 1-6 alkyl, and C 1-6 alkoxy, wherein alkyl and alkoxy are unsubstituted or substituted with one to five halogens, and wherein any methylene (CH 2 ) carbon atom in R 5 is unsubstituted or substituted with one to two groups independently selected from halogen, hydroxy, and C 1-4 alkyl unsubstituted or substituted with one to five halogens;

each R 6 is hydrogen or R 5 ; and

R 7 is selected from the group consisting of

hydrogen,

(CH 2 ) n -phenyl,

(CH 2 ) n —C 3-6 cycloalkyl, and

C 1-6 alkyl,

2. The compound of claim 1 wherein the carbon atom marked with an * has the stereochemical configuration as depicted in formula IIa:

3. The compound of claim 1 of structural formula IIb:

4. The compound of claim 3 wherein X is CH 2 , CHF, or CF 2 and R 1 is hydrogen.

5. The compound of claim 3 wherein the carbon atom marked with an * has the stereochemical configured as depicted in formula IIc:

and wherein X is CH 2 , CHF, or CF 2 and R 1 is hydrogen.

6. The compound of claim 1 of structural formula Id:

7. The compound of claim 6 wherein X is CH 2 , CHF, or CF 2 and R 1 is hydrogen.

8. The compound of claim 6 wherein the carbon atom marked with an * has the stereochemical configuration as depicted in formula IIe: