Skip to content
BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Mannich Reaction with 5,5-Dimethyl-3-phenylamino-2-cyclohexen-1-one

  • W. S. Hamama , M. Hammouda and E. M. Afsah

Abstract

Mannich reaction of the title compound 1 with morpholine, piperidine or piperazine gave the keto-bases 2-4, respectively. Whereas, such reaction with primary amines afforded the quinazolinones 5 and 6. Compound 1 reacts with isonicotinic acid hydrazide and formalin to give 7. Schmidt reaction of 4 and 5a gave 8 and 9, respectively. Reduction of the latter afforded the 9H-pyrimido[5,4-ḇ]azepine ring system 10. The reaction of 1 with formalin was investigated.

Received: 1986-8-18
Revised: 1987-10-26
Published Online: 2014-6-2
Published in Print: 1988-4-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Downloaded on 28.4.2024 from https://www.degruyter.com/document/doi/10.1515/znb-1988-0417/html
Scroll to top button