82436-33-7Relevant academic research and scientific papers
Smiles rearrangement of 2-(1-methyl-1H-tetrazol-5-ylthio)acetamides and their sulfonyl derivatives
Ishii,Hatanaka,Ueda
, p. 3331 - 3334 (2007/10/02)
The Smiles rearrangement of 2-(1-methyl-1H-tetrazol-5-ylthio)acetamides and their sulfonyl derivatives occurred under basic conditions to yield 5-amino-1-methyl-1H-tetrazole derivatives in excellent yields.
Antiulcer agents. II. Synthesis and gastric acid antisecretory activity of N-[3-{3-(piperidinomethyl)phenoxy}propyl]-4-(1-methyl-1H-tetrazol-5- ylthio)butanamide and related compound
Ueda,Ishii,Sinozaki,Seiki,Hatanaka
, p. 1430 - 1435 (2007/10/02)
N-[3-{3-(Piperidinomethyl)phenoxy}propyl]butamides having a 1-methyl-1H-tetrazol-5-ylthio moiety as a pharmacophore and related compounds were prepared and tested for their antisecretory activity against histamine-induced gastric acid secretion in conscious rats with gastric fistulas. Most of the compounds showed antisecretory activity. Among them, N-[3-{3-(piperidinomethyl)phenoxy}propyl]-4-(1-methyl-1H-tetrazol-5- ylthio)butanamide (5f) was found to possess the most potent activity, and a possibility of isosteric replacement of the methoxycarbonyl group with 1-methyl-1H-tetrazol-5-yl group was indicated. The structure-activity relationships are also discussed.
