http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-084606-A1

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filingDate 2011-12-27^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5da5dea38a5b59e4f438b848a75314c5
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publicationDate 2013-05-29^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-084606-A1
titleOfInvention BIARIL-AMIDA DERIVATIVES
abstract Process for obtaining the disclosed compound Claim 1: Compounds of the formula (1) in which: R 1 is alkyl, cycloalkyl, cycloalkylalkyl, alkoxyalkyl, cycloalkoxyalkyl, haloalkyl, haloalkoxyalkyl, halocycloalkyl, halocycloalkylalkyl, halocycloalkoxaryl, aryl, substituted aryl, aryl, substituted aryl substituted heteroaryl, said aryl and heteroaryl are substituted with one to three substituents independently selected from alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkoxyalkyl, cycloalkoxy, cycloalkoxyalkyl, alkylcycloalkylalkyl, halocycloalkyl, halocycloalkylalkyl, halogen, haloalkyl, hydroxy, hydroxyalkyl , alkoxy, alkoxyalkyl, haloalkoxy, hydroxyalkoxy, alkoxyalkoxy, alkoxyalkoxyalkyl, hydroxyhaloalkyl, amino and substituted amino, said substituted amino is substituted by one or two substituents independently selected from alkyl, cycloalkyl, alq uylcycloalkyl, cycloalkylalkyl, alkylcycloalkylalkyl, hydroxyalkyl and alkoxyalkyl; R2 is hydrogen, alkyl or cycloalkyl; R3 is hydrogen, alkyl or cycloalkyl; R4 is hydrogen, alkyl or cycloalkyl; R5 is hydrogen, alkyl or cycloalkyl; or R4 and R5 together with the carbon atom to which they are attached form a cycloalkyl; R6 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; R7 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; R8 is alkyl, cycloalkyl, cycloalkylalkyl, alkoxy, alkoxyalkyl, cycloalkoxy, cycloalkoxyalkyl, haloalkyl, haloalkoxy, haloalkoxyalkyl, halocycloalkyl, halocycloalkylalkyl, halocycloalkoxy, halocicloalcoxialquilo, alkoxycarbonyl, cycloalkoxycarbonyl, haloalkoxycarbonyl, halocicloalcoxicarbonilo, aryl, substituted aryl, heteroaryl or substituted heteroaryl, said aryl and heteroaryl are substituted with one to three substituents independently selected from alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkoxyalkyl, cycloalkoxy, cycloalkoxyalkyl, alkylcycloalkylalkyl, halocycloalkyl, halocycloalkylalkyl, halogen, haloalkyl, alkoxy, alkoxyalkyl, haloalkoxy, alkoxyalkoxy, alkoxyalkoxyalkyl, amino and substituted amino, said substituted amino is substituted by one or two substituents independently selected from alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl or, alkylcycloalkylalkyl, hydroxyalkyl and alkoxyalkyl; R9 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; R10 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; R11 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; R12 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; R13 is hydrogen, alkyl, alkoxy, cycloalkyl, halogen or cyano; A is CR13 or N; or its pharmaceutically acceptable salts. Claim 20: The use of a compound according to any one of claims 1 to 14 for the manufacture of a medicament for the treatment or prophylaxis of glomerulonephritis, the purple nephropathy of Henoch-Schönlein, the growing nephropathy associated with ANCA, the Lupus nephritis and IgA nephritis. Claim 22: A method of treatment or prophylaxis of glomerulonephritis, Henoch-Schönlein purple nephropathy, the increasing nephropathy associated with ANCA, lupus nephritis and IgA nephritis, said method consists of administering an effective amount of a compound according to any one of claims 1 to 14.
priorityDate 2010-12-27^^<http://www.w3.org/2001/XMLSchema#date>
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