http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5555191-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-052
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
filingDate 1978-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_12cde0019ce43bab179e7fc8c346d170
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fa29223188087f431fd9f445a813c48
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publicationDate 1980-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5555191-A
titleOfInvention Dihydropyranopyrazolidine derivative and its preparation
abstract NEW MATERIAL:A 1,2-diphenyl-dihydropyrano[2,3-c]pyrazolidine derivative of formula I (X 1 , 2 are H, halogen, lower alkyl, lower alkyloxy, or hydroxyl, provided that one of X 1 and X 2 is H). n EXAMPLE: 1,2-Diphenyl-3-oxo-5-hydroxy-6,6-dimethyl-5,6-dihydropyrano[2,3-c]- pyrazolidine. n USE: Drug having antiphlogistic and blood platelet coagulation activities. n PROCESS: The compound I is prepared by reacting a compound II (X is H, halogen, lower alkyl, lower alkyloxy, or OH), e.g. 1,2-diphenyl-3,5-dioxo-(2',3'-dioxo-3'- methyl)-butyl-pyrazolidine, with a base such as NaOH, in a solvent such as water or methanol, at 0W100°C. The compound II is novel, and can be obtained by reacting a compound III with a peroxide. n COPYRIGHT: (C)1980,JPO&Japio
priorityDate 1978-10-20-04:00^^<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: 31.