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filingDate 1995-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a7884ac76ff9ce8574ba94252a8a60a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a90f92d829e219d237537abb0864a3d
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publicationDate 1996-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0708104-A1
titleOfInvention Process and intermediate for the preparation of terazosin hydrochloride dihydrate
abstract A process for the preparation of 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-tetrahydrofuroyl)piperazine hydrochloride (terazosin hydrochloride dihydrate comprises the steps of reacting 4-amino-2-chloro-6,7-dimethoxy-quinazoline with N-(2-tetrahydrofuroyl)piperazine in an anhydrous polar organic solvent in the absence of an added acid scavenger to produce anhydrous 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-tetrahydrofuroyl)piperazine hydrochloride (Form IV) and thereafter converting the product of that step to 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-tetrahydrofuroyl)piperazine hydrochloride dihydrate.
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