Literature DB >> 18007485

Unexpected hydrazinolysis behaviour of 1-chloro-4-methyl-5H-pyridazino[4,5-b]indole and a convenient synthesis of new [1,2,4]-triazolo[4',3':1,6]pyridazino[4,5-b]indoles.

Hussein El-Kashef1, Abdelrahman A H Farghaly, Norbert Haider, Andrea Wobus.   

Abstract

Reaction of the title compound with hydrazine in the presence of air gives the 1-unsubstituted parent system via oxidative dehydrazination of the 1-hydrazino intermediate. The latter can be obtained in high yield by carrying out the hydrazinolysis step under inert gas, and it is smoothly converted into [1,2,4]-triazolo[4',3':1,6]pyridazino[4,5- b]indoles.

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Year:  2004        PMID: 18007485      PMCID: PMC6147308          DOI: 10.3390/91000849

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  2 in total

1.  Streptonigrin. 1. Structure-activity relationships among simple bicyclic analogues. Rate dependence of DNA degradation on quinone reduction potential.

Authors:  I A Shaikh; F Johnson; A P Grollman
Journal:  J Med Chem       Date:  1986-08       Impact factor: 7.446

2.  Degradation of propildazine in water.

Authors:  P Ventura; F Parravicini; L Simonotti; R Colombo; G Pifferi
Journal:  J Pharm Sci       Date:  1981-03       Impact factor: 3.534

  2 in total
  1 in total

1.  Construction of Unusual Indole-Based Heterocycles from Tetrahydro-1H-pyridazino[3,4-b]indoles.

Authors:  Cecilia Ciccolini; Lucia De Crescentini; Fabio Mantellini; Giacomo Mari; Stefania Santeusanio; Gianfranco Favi
Journal:  Molecules       Date:  2020-09-09       Impact factor: 4.411

  1 in total

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