Synthesis of Antimalarial Agents from 2,3-Dihydro-1,6-diazaphenalene Derivatives.

Abstract

The investigation to date has centered on construction of the 9H-1,6-diazaphenalene system and the more important 9-methoxy derivatives. By use of the oxime and Semmler Wolff approach outlined in our original proposal, the 1,6-diazaphenalone has been prepared, as well as the 5-amino quinoline derivative. In addition, work toward the 9-methoxy analogs has progressed quite well. Moreover, a two-step synthesis of dihydro-2,5-dihydroxy-1,6-diazaphenalene-1,6-dioxide has been developed. The Semmler Wolff product and the mono N-Oxide derivative of 26 have both been converted to 2,5-dichloro-1,6-diazaphenalene. Five systems will be converted to the diazaphenalene target compounds by standard methods during the second year.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 1979
Accession Number
ADA064248

Entities

People

  • James M Cook

Organizations

  • University of Wisconsin Milwaukee Department of Chemistry and Biochemistry

Tags

DTIC Thesaurus Topics

  • Alcohols
  • Amides
  • Amines
  • Anhydrides
  • Chemical Synthesis
  • Chemistry
  • Column Chromatography
  • Mass Spectra
  • Mass Spectroscopy
  • Organic Chemistry
  • Organic Compounds
  • Spectra
  • Spectroscopy

Fields of Study

  • Chemistry

Readers

  • Analytical Chemistry
  • Parasitology and Pharmacology of Malaria.