A NOVEL SYNTHESIS OF 1,8-ALKANОРYRIDO[З,4-<i>d</i>]PYRIDAZINE: NEW RING SYSTEM

Авторы

  • A. Z. A. Elassar Department of Chemistry, Faculty of Science, University of Kuwait, P. O. Box 5969-Safat-13060
  • Y. M. Elkholy Department of Chemistry, Faculty of Science, Helwan University, Ain Helwan, Cairo

Ключевые слова:

8-alkanopyrido[3,4-d]pyridаzinеs, cycloalkenopyridazines, cycloalkenopyridines

Аннотация

Cycloalkylidenemalononitrdes couple with various diazonium salts to yield the corresponding cycloalkeno[c]pyridazines, which react with trichloro-acetonitrile to give the 1,8-alkanopyrido[3,4-d]pyridazines. The reaction of cycloalkenopyridazines with DMF dimethylacetal gives enamine derivatives, which can be converted to 1,8-alkanopyrido[3,4-d]pyridaziries via treating with hydrazine hydrate оr aromatic amines. Substituted cycloalkenopyridines react with diazoaminobenzene to afford the corresponding 1,8-aikanоpyridopyri-dazines.

How to Cite
Elassar, A. Z. A.; Elkholy, Y. M. Chem. Heterocycl. Compd. 2002, 38, 1521. [Khim. Geterotsikl. Soedin. 2002, 1722.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1022657914710

Загрузки

Опубликован

2002-12-25

Выпуск

№ 12 (2002)

Раздел

Оригинальные статьи