http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5495561-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1374dd16777534b65ad4422333245af8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-333
filingDate 1978-01-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc73a53703b5cdb6582ae13ea7614f2c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd10080b788f1e6d38ebda3ca8544e0e
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publicationDate 1979-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5495561-A
titleOfInvention Acylated pyrrole derivative and its preparation
abstract NEW MATERIAL:Acylated pyrrole derivatives of formula I (R 1 is lower alkyl; R 2 is H or lower alkyl; R 3 is H or 2 - 10C acyl; Ar is 5 or 6 membered monoaromatic ring). n EXAMPLE: 2-]3-Benzoyl-2,5-dimethylpyrrole-1]-1-propanol. n USE: Analgesics, antiflammatory agents, antithrombotic agents, and antiarteriosclerosis. n PREPARATION: The condensation reaction of a pyrrole derivative of formula II (R 31 is H or 2 - 10C acyl) with an acylating agent selected from the groups consisting of aromatic carboxylic acids, acid halides and anhydrides is effected in the presence of an acidic catalyst as sulfuric or Lewis acid, when necessary, followed by hydrolysis to prepare an acylated pyrrole of formula I. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1978-01-10-04:00^^<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: 20.