Mendeleev Commun., 2022 Volume 32, Issue 2, Pages 265–267
(Mi mendc635)
This article is cited in
4 papers
Communications
New type of recyclization in 3,4-dihydroisoquinolines in the synthesis of β-(o-indazolylaryl)ethylamines and their 7-azaindazolyl analogues
A. A. Zubenko a ,
A. S. Morkovnik b ,
L. N. Divaeva b ,
V. S. Sochnev b ,
O. P. Demidov c ,
A. I. Klimenko a ,
L. N. Fetisov a ,
A. N. Bodryakov a ,
M. A. Bodryakova a ,
G. S. Borodkin b a North-Caucasian Zonal Research Veterinary Institute, Novocherkassk, Russian Federation
b Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
c North-Caucasus Federal University, Stavropol, Russian Federation
Abstract:
1-(2-Hydrazinoaryl)-3,4-dihydroisoquinolines and their hydrazinopyridyl analogues undergo recyclization affording novel (7-aza)indazolyl-β-arylethylamines. The products are expected to possess neurotropic activities.
Keywords:
1-(2-hydrazinoaryl)-3,4-dihydroisoquinolines, Isoquinolines, b-phenylethylamines, recyclization, indazoles, 7-azaindazoles.
Language: English
DOI:
10.1016/j.mencom.2022.03.038
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