http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1056904-A3

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C04B35-80
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04
filingDate 1980-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9556494086e5bce4bc807cf3d9a6946
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_585afffcbaa011ac88a550a5a772fcaf
publicationDate 1983-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1056904-A3
titleOfInvention Process for preparing derivatives of 1,4-diazepine
abstract A method for producing 1,4-diazepine derivatives with the general formula dvd R,. Xf is chlorine, bromine or C ;, is C2 j: al-where R is kil; 2 - hydrogen, chlorine, bromine, methyl, C „C cycloalkyl, tetrahydropyranyl, methylamine, ethyl: amine or diethylamine; R is fluorine or chlorine radical, characterized in that, in order to increase, yield and expand the assortment of the target product, the compound of the general formula where these values are f Hal is halogen, is reacted with hydroxylamine hydrochloride in the presence of potassium iodide and N, fi flHH3onpo-: with pilethylamine in organic S solvent at the boiling point (L nor the reaction mixture and the compound obtained with the general formula v RiHf W rt-M-Tj CH-lk co and o have the indicated values. where they are reacted with thionyl chloride or iodide 2- rum-1-methyl-4: ib pyridyl and 1,5-diazabicyclo 4,3,0 non-5-ene at a temperature .komnatnoy in an organic solvent.
priorityDate 1979-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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