http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2177003-C2

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filingDate 1996-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9fe7691b0697084601799c569c124378
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b3447f49a29449fc2f0c2154019becb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb21afe5a3c529586f1cdc5da35e7237
publicationDate 2001-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2177003-C2
titleOfInvention Method of synthesis of aminophenylsulfonylureas (variants), intermediate compounds
abstract FIELD: organic chemistry, chemical technology. SUBSTANCE: invention relates to a novel method of synthesis (its variants) of aminophenylsulfonylureas of the formula (I) eliciting properties as regulating agents of plant growth or herbicides and to intermediate compounds used for their synthesis. Method of synthesis of aminophenylsulfonylureas of the formula (I) where radical values are given in the invention claim involves treatment of compound of the formula (II) or its salt with halogenating agent to yield the corresponding carboxylic acid halogenide that is rearranged to yield the compound of the formula (III) . Then compound of the formula (III) is subjected for ammonolysis by the group SO 2 CL 2 to yield the compound of the formula (IV) followed by reduction of the group NO 2 in this compound to yield the compound of the formula (V) that is subjected for interaction with the corresponding carbamate or its salt of the formula (VI) where Ar means unsubstituted or substituted phenyl and M means hydrogen atom, C 1 -C 4 -alkyl or metal cation. Alternative method involves ammonolysis reaction of compound of the formula (III) by the group SO 2 CL 2 and the synthesized compound of the formula (IV) is subjected for interaction with the corresponding carbamate or its salt of the formula (VI) and synthesized compound of the formula (VII) is reduced. The another alternative method involves interaction of compound of the formula (III) with cyanate or heterocyclic amine of the formula (VIII) given in the invention claim to yield the compound of the formula (VII) that is reduced. Intermediate compounds corresponding to formulas (III), (IV), (V), (VI) and (VII) are the novel ones. Invention proposes also a method to synthesize the compound of the formula (I). EFFECT: improved method of synthesis, increased yield and good purity of compounds. 14 cl, 11 ex
priorityDate 1995-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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