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filingDate 1979-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e98eb632d098a98636c3777181dd9ea
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publicationDate 1981-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5677261-A
titleOfInvention 1 2h isoquinolone derivative and its acid addition salt
abstract NEW MATERIAL:A compound of formula I (Y is H, Cl or OCH3; Z is 2-4C bivalent saturated aliphatic hydrocarbon group; R1 is cyano, carbamoyl, phenyl, etc.; R2 is H or lower alkyl; R3 is lower alkyl; R2 and R3 may together form a heterocyclic group with adjacent N atom), and its acid addition salt. EXAMPLE:2-(3-N,N-Dimethylaminopropyl)-4-phenyl-1(2H)-isoquinoline tartrate. USE:Drug having excellent analgesic, antireesrpinic, antihistaminic, acetylcholinolytic, gastric juice secretion suppressing, and antiulcer activites. Dose: 0.5-50mg/kg daily for adult in 1-3 doses. PROCESS:The compound of formula I is prepared e.g. by the thermal reaction of a substituted-1(2H)-isoquinolone of formula II with a substituted-aminoalkyl halide of formula III in an organic solvent in the presence of a basic catalyst.
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Total number of triples: 47.