SYNTHESIS OF THIAZINO- AND THIAZOLOQUINAZOLINONES BY CYCLIZATION OF S-(2-PROPENYL) DERIVATIVES OF 2-THIOXO-2,3-DIHYDRO-4(1H)-QUINAZOLINONE

Authors

  • В. В. Орысык Uzhgorod State University, Uzhgorod 88000
  • Ю. Л. Зборовский Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev 02094
  • В. И. Станинец Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev 02094
  • А. А. Добош Uzhgorod State University, Uzhgorod 88000
  • С. М. Хрипак Uzhgorod State University, Uzhgorod 88000

Keywords:

thiazinoquinazolinones, thiazoloquinazolinones, cyclization, rearrangement

Abstract

Interaction of potassium salts of quinazolin-2-thiol-4-one with γ-substituted allyl halides gave thiazoloquinazolinones with linear or angular structures depending on the structure of the carbonyl radical. S-Allyl substituted quinazolin-2-thiol-4-one reacted with halogens to give iminium salts of thiazinoquinazolinone with an angular structure. The conversion of these salts to the corresponding
bases and thiazoloquinazolinones has been studied.

How to Cite
Orysyk, V. V.; Zborovskii, Yu. L.; Staninets, V. I.; Dobosh, A. A.; Khripak, S. M. Chem. Heterocycl. Compd. 2003, 39, 640. [Khim. Geterotsikl. Soedin. 2003, 739.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1025154317771

Published

2003-05-25

Issue

Section

Original Papers