Synthesis 1993; 1993(6): 568-570
DOI: 10.1055/s-1993-25905
short 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.

Synthesis of 3-Aminopyrrolo[2,1-a]isoquinoline, 3-Aminopyrrolo[2,1-a]phthalazine, and 7-Aminopyrrolo[1,2-b]pyridazine Derivatives

Alexander F. Khlebnikov* , Elena I. Kostik, Raphael R. Kostikov
  • *Department of Chemistry, St. Petersburg State University, Universitetskaya nab. 7/9, 199034 St. Petersburg, Russia
Further Information

Publication History

Publication Date:
17 September 2002 (online)

A simple route to 3-aminopyrrolo[2,1-a]isoquinoline, 3-aminopyrrolo[2,1-a]phthalazine, and 7-aminopyrrolo[1, 2-b]pyridazine derivatives 8a, 8b and 11, respectively, is described, based on displacement of a chlorine atom in the appropriate precursors with benzylamine. The chloro-substituted precursors were prepared by using a tandem dichlorocarbene/cycloimmonium ylide approach.

    >