
Monatshefte fur Chemie p. 187 - 198 (1981)
Update date:2022-08-04
Topics:
Zigeuner, Gustav
Schweiger, Klaus
Fuchsgruber, Alfred
The tautomers, 4-hydroxy-5,6-dihydro-6,6-dimethyl-2(1H)-pyridinethione (1) and 6,6-dimethyl-2-thioxo-4-piperidone (2) resp., and 4-hydroxy-5,6-dihydro-6,6-dimethyl-2(1H)-pyridone (9) and 6,6-dimethyl-2,4-piperidinedione (10) resp. were synthesized by hydrolysis of 4-amino-5,6-dihydro-6,6-dimethyl-2(1H)-pyridinethiones (4,5) and -ones (11,12). 1,2 and 9,10 undergo an aminolysis in amines to the corresponding 4-aminodihydro-2(1H)-pyridinethiones 4,5 and -ones 11, 12 resp. - Keywords: 6,6-Dimethyl-2,4-piperidindione; 6,6-Dimethyl-2-thioxo-4-piperidone; 4-Hydroxy-6,6-dimethyl-5,6-dihydro-2(1H)-pyridone, and -pyridinethione; Keto-enol-tautomeris m
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(1981)Doi:10.1021/jo01278a046
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(1981)