http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4454326-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7b4beef0c137d9094e6918ee382be22f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-36
filingDate 1982-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2838fb7d166184155d0f3f48ac511ca4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4ce87dfcd38a316dbeb687732e65085
publicationDate 1984-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4454326-A
titleOfInvention 5-Aroyl 6-chloro or 6-bromo 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-di-carboxylates
abstract 5-Substituted-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids of the formula ##STR1## wherein: X is hydrogen, lower alkyl, chloro or bromo; Ar is a moiety selected from the group consisting of ##STR2## in which: Y is oxygen or sulfur; n R is hydrogen, methyl, chloro, or bromo, the R substitution being at the 3, 4 or 5 position of the ring; n R 1 is hydrogen, lower alkyl, lower alkoxyl, lower alkoxycarbonyl, lower alkylcarbonyl, fluoro, chloro or bromo, the R 1 substitution being at any available position in the ring; n R 2 is hydrogen or lower alkyl; n are prepared by β-decarboxylation of the corresponding dialkyl-1,1-dicarboxylates. Certain substituted pyrroles are useful as intermediates for preparing the compounds of formula I.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5804214-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5962013-A
priorityDate 1981-06-11-04:00^^<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: 788.