http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2109738-C1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e404b57297e1d7ddf9ef360d5b19dc7
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D279-02
filingDate 1993-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6e2a69ad527d48b1a2f8dfd4da9313c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f75f44ceed29c122d77feeed6173c214
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef968dacf884bb3c96523a2b788f0c90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_589f8ba94fae6d8d68df06d80e57bd85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_888b54b8d2fdaaa56ba3a2016b9b6eca
publicationDate 1998-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2109738-C1
titleOfInvention Method of synthesis of 3-alkoxycarbonyl-4-hydroxy-2-methyl-2h- -1,2-benzothiazine-1,1-dioxides
abstract FIELD: chemistry of heterocyclic compounds. SUBSTANCE: product: 3-alkoxycarbonyl- -4-hydroxy-2-methyl-2H-1,2-benzothiazine-1,1-dioxides. Yield is 73%. Reagent 1: saccharin. Reagent 2: monochloroacetic acid ester. Reaction conditions: in medium of dimethylformamide, at increased temperature, in the presence of potassium carbonate, at equimolar ratio of reagents. Obtained reaction mixture is treated with sodium alcoholate and then with methylating agent. Synthesized compound is used for synthesis of intermediate nonsteroid compounds for synthesis of antiinflammatory agents. EFFECT: improved method of synthesis, high yield of product. 2 cl
priorityDate 1993-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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