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Chemistry of Heterocyclic Compounds

, Volume 1, Issue 2, pp 162–164 | Cite as

Phenothiazine syntheses. XVIII. 2-Aminophenothiazine derivatives

  • S. V. Zhuravlev
  • A. N. Gritsenko
Article
  • 46 Downloads

Abstract

2-(α-chloroacetylamido)-2-(β-chloropropionylamido)-2-(benzylideneamino)- and 2-(o-hydroxybenzyllideneamino)phenothiazines are synthesized and reduced by lithium aluminum hydride to 2-ethylamino-, 2-propylamino-, 2-benzylamino-, and 2-(o-hydroxybenzylamino)phenothiazine. Reduction of the methyl and ethyl esters of phenothiazinecarbamic-2 acid by lithium aluminum hydride gives 2-methylaminophenothiazine.

Keywords

Aluminum Methyl Ester Ethyl Lithium 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© The Faraday Press, Inc. 1966

Authors and Affiliations

  • S. V. Zhuravlev
    • 1
  • A. N. Gritsenko
    • 1
  1. 1.Institute of Pharmacology and Chemotherapy AMS USSRMoscow

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