Thianaphtheno [3, 2-c] pyridine and Certain Derivatives

DB Capps, CS Hamilton

Index: Capps; Hamilton Journal of the American Chemical Society, 1953 , vol. 75, p. 697

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Citation Number: 3

Abstract

2-Thianaphthenyl sodium was treated with ethylene oxide, giving 2-thianaphthene-ethanol. The alcohol was converted to its chloro analog and the latter to the iodo compound, which gave 2-thianaphthene-ethylamine by Gabriel's phthalimide reaction. 2-Thianaphthene- ethylamine was benzoylated and acetylated yielding amides which were converted to the corresponding dihydroisoquinoline-like compounds by the Bischler-Napieralski reaction. ...

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