US 5,705,515 A · Substituted sulfonamides as selective .beta.-3 agonists for the treatment of diabetes and obesity

Abstract

Substituted sulfonamides are selective .beta..sub.3 adrenergic receptor agonists with very little .beta..sub.1 and .beta..sub.2 adrenergic receptor activity and as such the compounds are capable of increasing lipolysis and energy expenditure in cells. The compounds thus have potent activity in the treatment of Type II diabetes and obesity. The compounds can also be used to lower triglyceride levels and cholesterol levels or raise high density lipoprotein levels or to decrease gut motility. In addition, the compounds can be used to reduced neurogenic inflammation or as antidepressant agents. The compounds are prepared by coupling an aminoalkylphenyl-sulfonamide with an appropriately substituted epoxide. Compositions and methods for the use of the compounds in the treatment of diabetes and obesity and for lowering triglyceride levels and cholesterol levels or raising high density lipoprotein levels or for increasing gut motility are also disclosed.

A compound having the formula I:

##STR62## where n is 0 to 5;
m is 0 or 1;
r is 0 to 3;
A is
(1) a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen, excluding pyridyl,
(2) a benzene ring fused to a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen, or
(3) a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen fused to a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen;
R.sup.1 is
(1) hydroxy,
(2) oxo,
(3) halogen,
(4) cyano,
(5) NR.sup.8 R.sup.8,
(6) SR.sup.8,
(7) trifluoromethyl,
(8) C.sub.1 -C.sub.10 alkyl,
(9) OR.sup.8,
(10) S(O).sub.t R.sup.9, where t is 1 or 2,
(11) OCOR.sup.9,
(12) NR.sup.8 COR.sup.9,
(13) COR.sup.9,
(14) NR.sup.8 SO.sub.2 R.sup.9,
(15) NR.sup.8 CO.sub.2 R.sup.8, or
(16) C.sub.1 -C.sub.10 alkyl substituted by hydroxy, halogen, cyano, NR.sup.8 R.sup.8, SR.sup.8, trifluoromethyl, OR.sup.8, C.sub.3 -C.sub.8 cycloalkyl, phenyl, NR.sup.8 COR.sup.9, COR.sup.9, S(O).sub.t R.sup.9, where t is 1 or 2, OCOR.sup.9, NR.sup.8 SO.sub.2 R.sup.9 or NR.sup.8 CO.sub.2 R.sup.8 ;
R.sup.2 and R.sup.3 are independently
(1) hydrogen,
(2) C.sub.1 -C.sub.10 alkyl or
(3) C.sub.1 -C.sub.10 alkyl with 1 to 5 substituents selected from hydroxy, C.sub.1 -C.sub.10 alkoxy, and halogen;
X is
(1) --CH.sub.2 --,
(2) --CH.sub.2 --CH.sub.2 --,
(3) --CH.dbd.CH-- or
(4) --CH.sub.2 O--;
R.sup.4 and R.sup.5 are independently
(1)hydrogen,
(2) C.sub.1 -C.sub.10 alkyl,
(3) halogen,
(4) NHR.sup.8,
(5) OR.sup.8
(6) S(O).sub.t R.sup.9, where t is 1 or 2, or
(7) NHSO.sub.2 R.sup.9 ;
R.sup.6 is
(1) hydrogen or
(2) C.sub.1 -C.sub.10 alkyl;
R.sup.7 is Z-(R.sup.1a).sub.n ;
R.sup.1a is
(1) R.sup.1,
(2) C.sub.3 -C.sub.8 cycloalkyl,
(3) phenyl optionally substituted with up to 4 groups independently selected from R.sup.8, NR.sup.8 R.sup.8, OR.sup.8, S(O).sub.t R.sup.8 where t is 0 to 2 and halogen, or
(4) 5 or 6-membered heterocycle with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen, optionally substituted with up to four groups independently selected from oxo, R.sup.8, NR.sup.8 R.sup.8, OR.sup.8, S(O).sub.t R.sup.8 where t is 0 to 2, and halogen;
Z is
(1) phenyl,
(2) naphthyl,
(3) a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen,
(4) a benzene ring fused to a C.sub.5 -C.sub.10 carbocyclic ring,
(5) a benzene ring fused to a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen,
(6) a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen fused to a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen, or
(7) a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen fused to a C.sub.5 -C.sub.10 carbocyclic ring;
R.sup.8 is
(1) hydrogen,
(2) C.sub.1 -C.sub.10 alkyl,
(3) C.sub.3 -C.sub.8 cycloalkyl,
(4) Z optionally having 1 to 5 substituents selected from halogen, nitro, oxo, NR.sup.10 R.sup.10, C.sub.1 -C.sub.10 alkyl, C.sub.1 -C.sub.10 alkoxy, C.sub.1 -C.sub.10 alkylthio, and C.sub.1 -C.sub.10 alkyl having 1 to 5 substituents selected from hydroxy, halogen, CO.sub.2 H, CO.sub.2 --C.sub.1 -C.sub.10 alkyl, SO.sub.2 --C.sub.1 -C.sub.10 alkyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.1 -C.sub.10 alkoxy, and Z optionally substituted by from 1 to 3 of halogen, C.sub.1 -C.sub.10 alkyl or C.sub.1 -C.sub.10 alkoxy, or
(5) C.sub.1 -C.sub.10 alkyl having 1 to 5 substituents selected from hydroxy, halogen, CO.sub.2 H, CO.sub.2 --C.sub.1 -C.sub.10 alkyl, SO.sub.2 --C.sub.1 -C.sub.10 alkyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.1 -C.sub.10 alkoxy, C.sub.1 -C.sub.10 alkyl, and Z optionally substituted by from 1 to 5 of halogen, trifluoromethyl, trifluoromethoxy, C.sub.1 -C.sub.10 alkyl or C.sub.1 -C.sub.10 alkoxy;
R.sup.9 is
(1) R.sup.8 or
(2) NR.sup.8 R.sup.8 ;
R.sup.10 is
(1) C.sub.1 -C.sub.10 alkyl, or
(2) two R.sup.10 groups together with the N to which they are attached formed a 5 or 6-membered ring optionally substituted with C.sub.1 -C.sub.10 alkyl;
or
a pharmaceutically acceptable salt thereof.

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Substituted sulfonamides as selective .beta.-3 agonists for the treatment of diabetes and obesity

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Substituted sulfonamides as selective .beta.-3 agonists for the treatment of diabetes and obesity

Life of this patent

Abstract

Claims13