http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1577696-A3

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08
filingDate 1986-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef6baec70f045257c7de2589949c1f78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2bec11f620eee7d0b0cc4feae54a2092
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37cd6587424130492981741b310e7fdb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_59503222a20abe8502caf15093ecc8e0
publicationDate 1990-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1577696-A3
titleOfInvention Method of obtaining derivatives of 3(2h) pyridazinon
abstract NEW MATERIAL:A pyridazinone derivative expressed by formula I [R1 is H, methyl, 3-6C alkenyl, 5-6C cycloalkyl, benzyl, phenyl, etc.; R2 is Cl or Br; Y1 and Y2 are H, 1-5C alkyl, 2-8C alkenyl, halogen, OR5 (R5 is H, 1-8C akyl, etc.), etc.; Y3 is 1-5C alkyl, 2-8C alkenyl, halogen, OR5, etc.] and salt thereof. EXAMPLE:4-Chloro-5-(3-methoxybenzylamino)-2-cyclopentyl-3(2H)pyridazin one. USE:With antagonism to chemical transmitters causing contraction of bronchial smooth muscles, etc., and useful as an antiallergic agent. PREPARATION:A compound expressed by formula II (Z is Cl or Br) is reacted with a benzylamine derivative expressed by formula III, as necessary, in the presence of a dehydrohalogenating agent in an inert solvent to afford the aimed compound expressed by formula I.
priorityDate 1985-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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