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filingDate 1978-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_371207fa12678d769dfb1472d3f84cf5
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publicationDate 1983-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1060115-A3
titleOfInvention Process for preparing derivatives of thienotriazolodiazepine or their acid addition salts
abstract 1456162 Thienodiazepines F HOFFMANNLA ROCHE & CO AG 7 Feb 1974 [8 Feb 1973] 05396/76 Divided out of 1456161 Heading C2C Compounds of the general formula (R 1 = halogen, NO 2 , NH 2 , alkanoyl; R 2 = pyridyl or thienyl optionally substituted adjacent to linking position, phenyl, o-trifluoromethylphenyl, o - halophenyl, o,o<SP>1</SP> - dihalophenyl, o - nitrophenyl; R 3 = H, OH, alkoxycarbonyl, alkanoyloxy; R 4 = H, alkyl, alkanoyl, hydroxyalkyl, mercaptoalkyl, alkoxycarbonyl, aminocarbonyl, haloalkyl, alkoxyalkyl, alkylthioalkyl, aralkoxyalkyl, cyanoalkyl, alkoxycarbonylalkyl, alkoxycarbonylaminoalkyl, alkylcarbonyloxyalkyl, aminocarbonyloxyalkyl, dialkylaminocarbonyloxyalkyl, CN, alkyl NR 5 R 6 , COO alkyl NR 5 R 6 , CONH alkyl NR 5 R 6 ; R 5,6 = H, alkyl, hydroxyalkyl or NR 5 R 6 = monocyclic saturated 5-6 membered ring optionally containing an oxygen or further nitrogen atom ; n = 0, 1) are prepared by standard methods, e.g. condensing the corresponding 5- aryl - 1,3 - dihydro - 2H - thieno[2,3-e] - 1,4- diazepine-2-thione with R 4 CONHNH 2 .
priorityDate 1973-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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