http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61263977-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00
filingDate 1985-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67485af2bd9ff1c8a61c88c817a23721
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_912122ba492a64a83c3b5c0b1a01ed5f
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publicationDate 1986-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61263977-A
titleOfInvention Dihydroimidazo(1,2-a)pyrimidine derivative
abstract NEW MATERIAL:The compound of formula I [R is H, 1W5C alkyl, heteroaryl, phenyl, etc.; R 1 is cyano, alkoxycarbonyl, etc.; R 2 is 1W4C alkyl, hydroxymethyl, acetoxymethyl, etc.; R 3 is 1W4C alkyl, formyl, nitro, etc.; R 4 or group of formula II (Rc and Rd are 1W4C alkyl, etc.; m is 1W3); n is 0W3]. n EXAMPLE: Methyl 3-diethylaminomethylaminomethyl-7-methyl-5-(3-nitrophenyl)- 5,8-dihydroimidazo[1,2-a]pyrimidine-6-carboxylate hydrochloride. n USE: A medicine. A remedy for coronary or cerebral circulatory disease. It has calcium antagonistic action, hypotensive action, coronary and cerebral vasodilating action and cardiotonic action, etc., and has low toxicity. n PREPARATION: For example, the compound of formula I can be produced by carrying out the electrophilic substitution reaction of the compound of formula III with an electrophilic reagent, thereby introducing the substituent group of formula IV to the imidazole ring. n COPYRIGHT: (C)1986,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006124354-A3
priorityDate 1985-05-16-04:00^^<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: 23.