http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009529045-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-94
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-94
filingDate 2007-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2009-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2009529045-A
titleOfInvention Process for synthesizing 7-alkynyl-4-aminoquinazolines and related intermediates
abstract A method of synthesizing 7-alkynyl-4-aminoquinazoline from 7-haloquinazoline is disclosed. As a specific synthesis of 1, from 7-chloro-6-nitro-3H-quinazolin-4-one to 4- [N-3-chloro-4-fluorophenyl]]-7- [3-methyl-3 -(4-Methyl-1-piperazinyl) -1-butynyl] -6- [N-inethylacrylamide] quinazoline is prepared. Intermediates useful in synthesizing 7-alkynyl-4-aminoquinazolines and methods for making the intermediates are also disclosed. 7-alkynyl-4-aminoquinazoline prepared by the method of the present invention is useful as a pharmaceutically active compound.
priorityDate 2006-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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