Synthesis of 10-substituted 5H-pyrido[3′,4′ :4,5]pyrrolo[2,3-g]isoquinolines
- 1 January 1979
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 1,p. 142-145
- https://doi.org/10.1039/p19790000142
Abstract
The preparation of 6-amino-5-methyl isoquinolin-1 (2H)-one is described. Starting from this key intermediate, several derivatives of 5H-pyrido[3′,4′ :4,5]pyrrolo[2,3-g]isoquinoline substituted with various alkyl amino-groups at their 10-position have been synthesized.This publication has 2 references indexed in Scilit:
- 6,11-Dimethyl-5H-pyrido[3′,4′:4,5]pyrrolo[2,3-g]isoquinoline: a new aza-analogue of ellipticineJournal of the Chemical Society, Perkin Transactions 1, 1979
- N-1 substitution of 4-arylamino-3-nitropyridines by a heterocyclic ring-opening reactionJournal of the Chemical Society, Perkin Transactions 1, 1979