Publication NumberUS 7638519
Assignees
  • Myogen, Inc.
StatusIssued Patent
Application Number11/018383
AvailabilityUnknown
Filing Date2004-12-21
Publication Date2009-12-29

Abstract

The present invention provides certain compounds, pharmaceutical formulations thereof, and methods for the treatment of conditions mediated by 5-HT2 receptors. These compounds provide for modulation of the signals mediated by 5-HT2 receptors, specifically those receptors in the cardiovascular system. Thus, these compounds may be used alone or in conjunction with other drugs to treat cardiovascular diseases such as, but not limited to, muscle atrophy, cardiac hypertrophy, heart failure, and primary pulmonary hypertension.

Claims

  • 1. A compound having the Formula I: and pharmaceutically acceptable salts thereof, wherein: R1 is NR8R9, wherein R8and R9 are each H; R2 is C1-6-alkyl, or C1-6-cycloalkyl; R3 is phenyl, pyridine, pyrimidine, thiophene, furan, oxazole, isoxazole, thiazole, isothiazole, imidazole, pyrazole and pyrrole, and any of R3 may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6-alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C0-6-alkyl-NH, (C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH—C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2—C1-6-alkyl, CONH—C0-6-alkyl, NHCO—C1-6-alkyl and COO—C0-6-alkyl; X and Y are null; R4 and R5 taken together form a thiophene, which may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C0-6-alkyl-NH, C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH—C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2-C1-6-alkyl, CONH—C0-6-alkyl, NHCO—C1-6-alkyl and COO—C0-6-alkyl; R6 and R7 are null, H, or are independently but not simultaneously phenyl, pyridine, pyrimidine, thiophene, furan, oxazole, isoxazole, thiazole, isothiazole, imidazole and pyrazole, and any of R6 or R7 may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6-alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C0-6-alkyl-NH, (C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH-C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2—C1-6-alkyl, CONH—C0-6-alkyl, NHCO-C1-6-alkyl and COO-C0-6-alkyl; alkyl may be straight or branched chain; further comprising all isomers, positional isomers, diastereomers, enantiomers and salts thereof; and excluding 3-methyl-2-phenyl-5,6,7,8-tetrahydro-benzo[4,5]thieno [2,3-b]pyridin-4-ylamine.
  • 2. The compound of claim 1, wherein R3 is phenyl, pyridine, thiophene or furan and any of R3 may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6-alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C0-6-alkyl-NH, (C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH—C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2—C1-6-alkyl, CONH-C0-6-alkyl, NHCO—C1-6-alkyl and COO—C0-6-alkyl.
  • 3. The compound of claim 1, wherein R6 and R7 are H.
  • 4. A pharmaceutical composition comprising at least one compound of the formula below or a physiologically acceptable salt thereof in an amount effective to relieve said condition together with at least one physiologically acceptable carrier or exipient: and pharmaceutically acceptable salts thereof, wherein: R1 is NR8R9, wherein R8 and R9 are each H; R2 is C1-6-alkyl or C1-6-cycloalkyl; R3 is phenyl, pyridine, pyrimidine, thiophene, furan, oxazole, isoxazole, thiazole, isothiazole, imidazole, pyrazole and pyrrole, and any of R3 may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6-alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C0-6-alkyl-NH, (C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH—C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2-C1-6-alkyl, CONH—C0-6-alkyl, NHCO—C1-6-alkyl and COO—C0-6-alkyl; X and Y are null; R4 and R5 taken together form a thiophene ring, which may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6-alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C0-6-alkyl-NH, (C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH—C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2—C1-6-alkyl, CONH—C0-6-alkyl, NHCO-C1-6-alkyl and COO—C0-6-alkyl; R6 and R7 are null, H, or are independently but not simultaneously phenyl, pyridine, pyrimidine, thiophene, furan, oxazole, isoxazole, thiazole, isothiazole, imidazole and pyrazole, and any of R6 or R7 may be optionally substituted by one or more of halogen, NO2, CN, CF3, C1-6-alkyl, C0-6-alkyl-S, C0-6-alkyl-O, C06-alkyl-NH, (C1-6-alkyl)2-N, C1-6-alkyl-SO, C1-6-alkyl-SO2, SO2NH—C0-6-alkyl, SO2N(C1-6-alkyl)2, NHSO2—C1-6-alkyl, CONH—C0-6-alkyl, NHCO—C1-6-alkyl and COO—C0-6-alkyl; alkyl may be straight or branched chain; further comprising all isomers, positional isomers, diastereomers and enantiomers.