Synthesis 1990; 1990(12): 1135-1137
DOI: 10.1055/s-1990-27114
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

A Facile and Convenient Synthetic Method for Fluorine-Containing Benz[c]acridines and Dihydrobenz[c]acridines from N,N-Dimethyl-1-naphthylamine

Masaru Hojo* , Ryoichi Masuda, Etsuji Okada, Takeshi Tomifuji, Naonori Imazaki
  • *Department of Industrial Chemistry, Faculty of Engineering, Kobe University, Kobe 657, Japan
Further Information

Publication History

Publication Date:
02 May 2002 (online)

Aromatic nucleophilic nitrogen-nitrogen exchange reaction of N,N-dimethyl-2, 4-bis(trifluoroacetyl)-1-naphthylamine (1) with p-substituted anilines gives the corresponding N-aryl-2,4-bis(trifluoroacetyl)-1-naphthylamines 2 in high yield. Acid-catalyzed cyclization of 2 affords selectively fluorine-containing benz[c]acridines 3 in almost quantitative yield, while the base-catalyzed cyclization gives fluorine-containing 7,12-dihydrobenz[c]acridines 4 in fair yield.

    >