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Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-82
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-82
filingDate 1972-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9273846ffcd7efe61eec803b13dfb574
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91ada43523fc5c925c93cd09f3d8a346
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3aed5c2db25f11b829e573e5b9b69a5f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6770f465efbf637ad8475071958657be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b008784080c1ef4b1d37ed757832e84c
publicationDate 1973-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-539638-A
titleOfInvention Process for the preparation of quinazoline derivatives
abstract Cpds. of gen. formula (I): (where R = polyhaloalkyl; R1 and R2 = H, hal., hal, NO2, CF3, lower alkyl, alkoxy, alkylthio or alkylsulphonyl; R3 = C6H4R4; R4 = H, hal., lower alkyl- or alkoxy, cycloalkyl, pyridyl, furyl or thienyl; W = -O or -S) are prepd. by reacting a cpd. (II) with R-OH; or by reaction of a cpd. (III) where X = -O or imino; with a cpd. with an OCN- or SCN- group in the molecule or, when X = imino, by reaction of (III) with a cpd. (Y) YZ-C=W where Y and Z=Cl, benzyloxy, CCl3, imidazolyl-1, lower alkoxy or alkylthio.
priorityDate 1971-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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