Substituted bicylic thiophene derivatives, compositions containing such compounds and methods of use
View Patent ↗The present invention addresses substituted thiophene derivatives, as well as compositions containing such compounds and methods of treatment. The compounds in the present invention are glucagon antagonists. The compounds block the action of glucagon at its receptor and thereby decrease the levels of plasma glucose providing a treatment of diabetes.
1. A compound represented by formula I:
or a pharmaceutically acceptable salt or solvate thereof wherein:
X is NR 4 ;
R 1 is selected from the group consisting of: H, C 1-10 alkyl, C 3-7 cycloalkyl and Aryl, said alkyl, cycloalkyl and Aryl being optionally substituted with 1-4 substituents independently selected from R 13 ;
R 2 is selected from the group consisting of: R 1 as defined above, —C(O) 2 R 7 and —CONR 7 R 8 ;
m is 0;
n is 3;
R 3 is selected from the group consisting of: C 1-10 alkyl, C 3-7 cycloalkyl and Aryl, said alkyl, cycloalkyl and Aryl being optionally substituted with 1-4 substituents selected from R 13 , such that when R 3 represents C 1-10 alkyl substituted with one R 13 group, and R 13 represents halo, R 1 , R 2 , R 5 and R 6 do not represent C 1-3 alkyl;
R 4 is selected from the group consisting of: C 3-10 alkyl, C 3-7 cycloalkyl, Aryl, HAR, Hetcy, C(O)C 5-10 alkyl, C(O)C 3-7 cycloalkyl, C(O)-Aryl, C(O)-HAR, C(O)-Hetcy, CONR 9 R 10 , CO 2 R 9 and SO 2 R 9 , the alkyl, cycloalkyl, Aryl, HAR and Hetcy groups and portions being optionally substituted with 1-4 substituents selected from R 13 ;
one of R 5 and R 6 is selected from the group consisting of NR 11 R 12 , NR 11 COR 12 , NR 11 CO 2 R 12 and NR 11 S(O) 2 R 12 , and the other represents R 1 , HAR, Hetcy or OR 11 , said HAR and Hetcy being optionally substituted with 1-4 substituents selected from R 13 ,
R 7 , R 10 and R 11 are selected from the group consisting of: R 1 as defined above, HAR and Hetcy, said HAR and Hetcy being optionally substituted with 1-4 substituents selected from R 13 ;
R 8 , R 9 and R 12 are selected from the group consisting of: C 1-10 alkyl, C 3-7 cycloalkyl, Aryl, HAR and Hetcy, said alkyl, cycloalkyl, Aryl, HAR and Hetcy being optionally substituted with 1-4 substituents selected from R 13 ;
or alternatively, R 7 , R 8 , R 9 and R 10 are as defined above, and R 11 and R 12 are taken together with the atoms to which they are attached along with any intervening atoms and represent a 5-8 membered ring optionally containing 1-2 heteroatoms selected from O, S and N, and optionally substituted with 1-4 substituents selected from R 13 ;
each R 13 is selected from the group consisting of: halo, NR 14 R 15 , C 1-4 alkyl, C 3-7 cycloalkyl, Aryl, HAR, Hetcy, CF 3 , OCF 3 , OR 15 , NO 2 , S(O) x R 14 , SR 14 , S(O) x NR 14 R 15 , O(CR 16 R 17 ) y NR 14 R 15 , C(O)R 14 , CO 2 R 15 , CO 2 (CR 16 R 17 )yCONR 14 R 15 , OC(O)R 14 , CN, C(O)NR 14 R 15 , NR 15 C(O)R 14 , NR 15 C(O)OR 14 , NR 15 C(O)NR 16 R 14 and CR 15 (N—OR 14 ), wherein x is 1 or 2, and y is an integer from 1-4,
said alkyl, cycloalkyl, Aryl, HAR and Hetcy being optionally substituted with 1-4 substituents selected from R 18 ;
R 14 , R 15 , R 16 and R 17 are independently selected from the group consisting of: H, C 1-10 alkyl, C 3-7 cycloalkyl, Aryl and Ar—C 1-10 alkyl;
and each R 18 is independently selected from the group consisting of: halogen, CN, C 1-4 alkyl, OH, CF 3 , Aryl, Aryloxy, CO 2 H and CO 2 C 1-4 alkyl, said Aryl and the Aryl portion of Aryloxy being optionally substituted with up to 4 halo groups, and up to 2 C 1-4 alkyl, OH, CF 3 or CN groups.
2. A compound in accordance with claim 1 wherein R 1 is selected from the group consisting of: H, C 1-10 alkyl, C 3-6 cycloalkyl and phenyl, said alkyl and phenyl being optionally substituted with 1-3 substituents selected from R 13 .
3. A compound in accordance with claim 1 wherein R 2 is H.
4. A compound in accordance with claim 1 wherein R 3 is C 3-10 alkyl optionally substituted with 1-4 substituents selected from R 13 , such that when R 3 is substituted with one R 13 group, and R 13 represents halo, R 1 , R 2 , R 1 and R 6 do not represent C 1-3 alkyl.
5. A compound in accordance with claim 4 wherein R 3 represents C 3-5 alkyl, optionally substituted with 1-4 R 13 groups.
6. A compound in accordance with claim 1 wherein R 4 is selected from the group consisting of: C 5 s 10 alkyl, C 3-6 cycloalkyl, phenyl, HAR, Hetcy, C(O)C 5-10 alkyl, C(O)C 3-6 cycloalkyl and CO 2 9 , the alkyl, cycloalkyl and, Aryl groups and portions, phenyl, HAR and Hetcy being optionally substituted with 1-4 substituents selected from R 13 , and R 9 representing C 1-10 alkyl, C 3-7 cycloalkyl, Aryl, HAR or Hetcy, said alkyl, cycloalkyl, Aryl groups and portions, HAR and Hetcy being optionally substituted with 1-4 R 13 groups.
7. A compound in accordance with claim 1 wherein R 13 is selected from the group consisting of: halo, C 1-4 alkyl, C 3-7 cycloalkyl, Aryl, HAR, Hetcy, and OR 15 wherein R 15 is H,
said alkyl, cycloalkyl, Aryl, HAR and Hetcy being optionally substituted with 1-4 substituents selected from R 18 and
R 18 is halo, C 1-4 alkyl, Aryl or CO 2 C 1-4 alkyl.
8. A compound in accordance with claim 1 selected from the group consisting of: tert-butyl 3-cyano-2-[(2-ethylbutanoyl)amino]-5,6-dihydrothieno[2,3-b]pyridine-7(4H) carboxylate; N-(3-cyano-7-isobutyl-4,5,6,7-tetrahydrothieno[2,3-b]pyridin-2-yl)-2-ethylbutanamide; and N-(3-cyano-7-isopropyl-4,5,6,7-tetrahydrothieno[2,3-b]pyridin-2-yl)-2-ethylbutanamide.
9. A pharmaceutical composition which is comprised of a compound in accordance with claim 1 in combination with a pharmaceutically acceptable carrier.
10. A method of treating type 2 diabetes mellitus in a mammalian patient in need of such treatment, comprising administering to said patient a compound in accordance with claim 1 in an amount that is effective to treat type 2 diabetes mellitus.