Restricted Rotation in Aryl Amines. XXII. N-Benzenesulfonyl-N-carboxymethyl-3-amino-2, 4, 6-trimethylpyridine and its N-Oxide
R Adams, JE Dunbar
Index: Adams; Dunbar Journal of the American Chemical Society, 1958 , vol. 80, p. 3649
Full Text: HTML
Citation Number: 1
Abstract
N, N-dibenzenesulfonyl-3-amino-2, 4, 6-trimethylpyridine (V). When two moles of benzenesulfonyl chloride was used V was obtained in 79% yield. Compound V was in turn converted to N-benzene-sulfonyl-3-amino-2, 4, 6-trimethylpyridine (VI) by boiling with sodium ethoxide in ethanol sofution. Conversion of VI to N-benzenesulfonyl-N- carbomethoxymethyl-3-amino-2, 4, 6-trimethylpyridine was accomplished by treatment ...
Related Articles:
Preparation of quinol imide acetates. VI. Scope and limitations
[Adams; Werbel Journal of the American Chemical Society, 1958 , vol. 80, p. 5799,5802]