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Heterocyclic amide derivatives as antagonists of the P2X7 receptor
专利权人:
ACTELION PHARMACEUTICALS LTD.
发明人:
申请号:
ARP130100155
公开号:
AR089753A1
申请日:
2013.01.18
申请国别(地区):
AR
年份:
2014
代理人:
摘要:
Claim 1: a compound of the formula (1), where n represents 1 or 2; X represents - N - O - N - (OR); r u00b9 represents Hydrogen or Halogen; R u00b2 represents Hydrogen or Methyl; and r u00b3 represents: aryl alkyl c u2081 u208b u2083, which is in the Mono alkyl, optionally substituted with Hydroxy Or heterociclilo; and which is in the aryl mono -, di - or tri substituted- Where the substituents are selected independently from the group consisting of c u2081 u208b u2084 alquenilo c u2082 u208b u2084, alkyl, cycloalkyl c u2083 u208b u2086 c u2081 u208b u2084 alkoxy alkyl, Hydroxy, alkoxy c u2082 u208b u2083 c u2081 u208b u2083, Hydroxy, alkoxy alkyl c u2081 u208b u2082 c u2082 u208b u2083 Hydroxy, alkoxy c u2081 u208b u2082 alq Uilo c u2081 u208b u2082, fluoroalquilo c u2081 u208b u2083, fluoroalcoxi c u2081 u208b u2083, cyano, halogen and c u2081 u208b u2083 heteroaryl alkyl phenoxy; or,Which is in the heterociclilo mono - alkyl substituted; and which is in part heteroaryl mono -, di - or tri - substituted - Where the substituents are selected independently from the group consisting of c u2081 u208b u2084 c u2083 u208b u2086 alkoxy alkyl, cycloalkyl, c u2081 u208b u2084, fluoro C u2081 u208b u2083 Halogen or alkyl and cycloalkyl c u2083 u208b u2087;, which is replaced with mono -, - C (o) or a nh u2082 phenyl optionally mono -,Di - or tri substituted, where the substituents are selected from Halogen, which is c u2085 u208b u2087 or cycloalkyl, optionally substituted mono - or Hydroxy and oxo; which is hybridized with a phenyl optionally mono -, di - or tri substituted, where the substituents are selected from Halogen Cicloalquil c u2083 u208b u2087 alkyl c u2081 u208b u2083; or,In the part which is optionally substituted with Hydroxy alkyl mono -; and which is in the di substituted cycloalkyl optionally with Halogen and optionally substituted with Hydroxy mono -, aryl or heteroaryl, aryl or heteroaryl groups which are optionally mono -, di - or tr I - replaced with H
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