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filingDate 1968-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4da7ae2baf2551f6d2e14c24e1771de5
publicationDate 1971-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-503737-A
titleOfInvention Process for the preparation of new derivatives of benzenesulfonamide
abstract (A) Cpds. of the general formula (I) R' = (1-4C)alkyl, (3-4C) alkenyl or (5-7C) cycloalkyl R2 = H, Me or Et X = H, F, Cl, Br, Me, MeS, MeO or CH3CO (B) Acid addn. salts of I. Oral and parenteral hypoglycaemics. Dose 100-500 mg/d. N-(2-methylaminoethyl)-p-methoxybenzene-sulphonamide (24.4 g.) was stirred with BrCN (10.6 g.) and 2N-NaOH (100 ml) at 20-30 deg., filtered, and recryst. from MeOH, giving the imidazoline, m.p. 104-7 deg.
priorityDate 1968-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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