1950
DOI: 10.1021/ja01167a011
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The Preparation of Heterocyclic Sulfonamides1

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Cited by 235 publications
(60 citation statements)
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“…Recently a series of more active carbonic anhydrase inhibitors of the sulfonamide group has been developed (11). One of these, the heterocyclic sulfonamide, 6063 (2-acetylamino-1,3,4-thiadiazole-5-sulfonamide), is a carbonic anhydrase inhibitor which is 50 to 400 times more effective than sulfanilamide and nontoxic in effective doses (12).…”
mentioning
confidence: 99%
“…Recently a series of more active carbonic anhydrase inhibitors of the sulfonamide group has been developed (11). One of these, the heterocyclic sulfonamide, 6063 (2-acetylamino-1,3,4-thiadiazole-5-sulfonamide), is a carbonic anhydrase inhibitor which is 50 to 400 times more effective than sulfanilamide and nontoxic in effective doses (12).…”
mentioning
confidence: 99%
“…The title compound (1) was isolated as an impurity in the chemical synthesis of the commercial diuretic known by its generic name of acetazolamide (2) (Roblin & Clapp, 1950).…”
Section: Commentmentioning
confidence: 99%
“…The synthesis of 5-amino-l,3,4-thiadiazole-2-sulfonamide (Hats) was originally described by Roblin & Clapp (1950). We have obtained Hats by a different method, following that published by Young, Wood, Eichler, Vaughan & Anderson (1956) for other 1,3,4-thiadiazolesulfonamides.…”
Section: Commentmentioning
confidence: 99%