1981
DOI: 10.1135/cccc19811188
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Synthesis of arylthioacetamidoximes as potential antidepressants

Abstract: Reactions of thiophenol and 16 of its derivatives with chloroacetonitrile afforded arylthioacetonitriles IVb-XXb which were treated with hydroxylamine and gave arylthioacetamidoximes IVa-XXa. Compounds VIIa-IXa, XIIa, XVIa and XVIIIa exhibited antireserpine activity in the test of ptosis in mice and compounds IXa and XVIIa in the test of reserpine hypothermia in mice.

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Cited by 4 publications
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“…-Methyl 3-amin0-2-cyano-4-phenyIsulfinylbut-Zenoa te38 Phenyl cyanomethyl sulfoxide 37 (0.495 g, 3 mmol) was added to a stirred solution of magnesium methoxide [from magnesium (0.072 g, 3 mmol) and anhydrous methanol (12 cm-')]. Methyl cyanoacetate (0.297 g, 3 mmol) was then added and the solution was refluxed for 20 h. The solvent was evaporated and the residue was washed with diethyl ether.…”
mentioning
confidence: 99%
“…-Methyl 3-amin0-2-cyano-4-phenyIsulfinylbut-Zenoa te38 Phenyl cyanomethyl sulfoxide 37 (0.495 g, 3 mmol) was added to a stirred solution of magnesium methoxide [from magnesium (0.072 g, 3 mmol) and anhydrous methanol (12 cm-')]. Methyl cyanoacetate (0.297 g, 3 mmol) was then added and the solution was refluxed for 20 h. The solvent was evaporated and the residue was washed with diethyl ether.…”
mentioning
confidence: 99%