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filingDate 1978-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1978-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-469111-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF NEW 2,5-DIHYDRO-1,2-THIAZINO (5,6-B) INDOL-3-CARBOXAMIDE-1,1-DIOXIDES.
abstract Compounds of the formula < IMAGE > WHEREIN R1 is hydrogen, methyl or ethyl R2 is methyl or ethyl Y is hydrogen, fluorine, chlorine, bromine, methoxy, methyl, ethyl or trifluoromethyl and Ar is 2-thiazolyl which may have one or two methyl or ethyl substituents attached thereto 5,6-dihydro-4H-cyclopentathiazol-2-yl 4,5,6,7-tetrahydro-2-benzothiazolyl 2-benzothiazolyl 3-isothiazolyl which may have a methyl substituent attached thereto 2-pyridyl which may have a methyl or hydroxyl substituent attached thereto 3-pyridyl 4-pyridyl 4-pyrimidinyl pyrazinyl 2-benzimidazolyl 2-oxazolyl which may have a methyl substituent attached thereto 2-benzoxazolyl or phenyl which may have a fluoro, chloro, bromo, methyl, ethyl, trifluoromethyl or methoxy substituent attached thereto and non-toxic, pharmacologically acceptable salts thereof formed with inorganic or organic bases. The compounds as well as their salts are useful as antiphlogistics and blood platelet aggregation inhibitors.
priorityDate 1977-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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