http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0230898-A1

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filingDate 2001-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a38dd058c8dcf38ad038ff6c83594f1a
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publicationDate 2002-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0230898-A1
titleOfInvention N-(4-aryloxypiperidin-1-ylalkyl) cinnamic amides as ccr33 receptor antagonists
abstract Compounds of formula (I) in free or salt form, where Ar1 is phenyl substituted by one or more substituents selected from halogen, cyano, nitro, and C¿1?-C8-alkyl optionally substituted by cyano or halogen, Ar?2¿ is phenyl optionally which is unsubstituted or substituted by one or more substituents selected from halogen, cyano, hydroxy, nitro, C¿1?-C8-alkyl, C1-C8-haloalkyl, C1-C8-alkoxy or C1-C8-alkoxycarbonyl, R?1 is C¿1-C8-alkyl substituted by hydroxy, C1-C8-alkoxy, acyloxy, -N(R2)R3, halogen, carboxy, C¿1?-C8-alkoxycarbonyl, phenyl- C1-C8-alkoxycarbonyl, -CON(R?4)R5¿ or by a monovalent cyclic organic group, R?2 and R3 ¿ are each independently hydrogen or C¿1?-C8-alkyl, or R?2¿ is hydrogen and R3 is acyl or SO¿2?R?6, or R2 and R3¿ together with the nitrogen atom to which they are attached denote a 5- or 6-membered heterocyclic group, R?4 and R5¿ are each independently hydrogen, C¿1?-C8-alkyl optionally substituted by hydroxy or phenyl, or phenyl optionally substituted by C1-C8-alkyl, halogen, cyano or C1-C8-alkoxy, or R?4 and R5¿ together with the nitrogen atom to which they are attached denote a 5- or 6-membered heterocyclic group, R6 is C1-C8-alkyl, C1-C8-haloalkyl, or phenyl optionally substituted by C1-C8-alkyl, and n is 1, 2, 3 or 4. The compounds are useful as pharmaceuticals.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100360521-C
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03007939-A1
priorityDate 2000-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 554.