INVESTIGATIONS ON PREPARATION AND REACTIV ITY OF C-ANELLATED DERIVATIVES OF 1,3,4-BENZOTRIAZEPINES AND RELATED PRECURSORS N,N-COUPLED HETEROBICYCLES FROM CYCLIC HYDRAZINE DERIVATIVES .12.

Citation
O. Morgenstern et al., INVESTIGATIONS ON PREPARATION AND REACTIV ITY OF C-ANELLATED DERIVATIVES OF 1,3,4-BENZOTRIAZEPINES AND RELATED PRECURSORS N,N-COUPLED HETEROBICYCLES FROM CYCLIC HYDRAZINE DERIVATIVES .12., Die Pharmazie, 51(7), 1996, pp. 458-467
Citations number
24
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
ISSN journal
00317144
Volume
51
Issue
7
Year of publication
1996
Pages
458 - 467
Database
ISI
SICI code
0031-7144(1996)51:7<458:IOPARI>2.0.ZU;2-N
Abstract
c-Anellated 1,3,4-benzotriazepines are hitherto unknown. In order to s ynthesize derivatives of pyrazolo[1,2-c]- and phthalazino[2,3-c][1,3,4 ]benzotriazepines the intramolecular cyclization of N-(N-arylthiocarba moyl)-pyrazolidines and -1,2,3,4-tetrahydrophthalazines, respectively, is investigated. The latter are prepared by reaction of pyrazolidine and 1,2,3,4-tetrahydrophthalazine, respectively, with 2-functionalized phenylisothiocyanates. Often the formation of derivatives of 3,1-benz othiazines prevented by employment of suitable precursors is observed.