http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-485163-A1

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filingDate 1979-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1980-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-485163-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF A NEW 5H-2,3-BENZODIAZEPINE DERIVATIVE OR OF AN ACID ADDITION SALT
abstract Procedure for the preparation of a new 5H-2,3-benzodiazepine derivative of general formula (I): **(Formula)** in which: R represents a hydrogen atom, a C1-5'' alkyl group, dialkylaminoalkyl, amino, alkylamino or dialkylamino, a styryl, phenyl-C1-3-alkyl or aryl group optionally provided with 1 to 3 halogen, hydroxyl, acyloxy, methyl, trifluoromethyl, nitro, amino, methylenedioxy, C1-4 alkoxy and/or aralkoxy substituents , or a heterocyclic group containing 1 or 2 nitrogen, oxygen and/or sulfur atoms, R1 represents a hydrogen atom or a C1-4 alkyl, hydroxymethyl, formyl, carboxyl, carbalkoxy, aryl, or heterocyclic group, R2 represents a hydrogen atom or a C1-4 alkyl, dialkylaminoalkyl, alkylamino, dialkylamino or aryl group, and R3 and R4 each represent a hydrogen atom, a halogen atom or a nitro, amino, hydroxyl, acyloxy, C1-3 alkyl, C1-5 alkoxy, dialkylaminoalkoxy or aralkoxy.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2036137-A1
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Total number of triples: 30.