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filingDate 1977-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed6735dc426c6717ec8b04c2e9ee95a0
publicationDate 1980-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-202074-B2
titleOfInvention Method of producing 2-/4-/2-furoyl/piperazin-1-yl/-amino-6,7-dimethoxy-quinazoline
abstract Novel compounds of the general formula II <IMAGE> in which X represents a chlorine, bromine or iodine atom, and n denotes an integer from 1 to 3, are obtained by reacting a 6,7-dimethoxyquinazoline with a halogen-substituted furan. The compounds obtained can then be reacted at a temperature from 0 DEG to 150 DEG C with hydrogen in the presence of a catalytic amount of a dehalogenating catalyst and in the presence of a solvent which is inert to the reaction. The compound 2-[4-(2-furoyl)piperazin-1-yl]-4-amino-6,7-dimethoxy-quinazoline which can be prepared according to the invention is in general useful on account of its ability to lower the blood pressure in mammals having high blood pressure.
priorityDate 1976-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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