New Functionalized Amino Derivatives of 2-Hydroxyphenyl-1,3,5-triazines

被引：1
|
作者：
Shasheva, E. Yu. [1 ]
Vikrishchuk, N. I. [1 ]
Popov, L. D. [1 ]
Borodkin, S. A. [1 ]
机构：
[1] Southern Fed Univ, Ul Zorge 7, Rostov Na Donu 344090, Russia
来源：
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 53卷 / 10期
关键词：
INHIBITION; DOCKING;
D O I：
10.1134/S107042801710013X
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
4-(2-Hydroxyphenyl)-1,3,5-triazin-2-ylcyanamides reacted with sodium azide to give N-(tetrazol-5-yl)-1,3,5-triazin-2-amines, and their reaction with allyl bromide afforded allyl(1,3,5-triazin-2-yl)cyanamides. Acetylation of 4-(2-hydroxyphenyl)-1,3,5-triazin-2-amines involved only the amino group with formation of diacetylamino derivatives, whereas the phenolic hydroxy group remained intact. The reaction of triazinamines with 2,5-dimethoxytetrahydrofuran in the presence of P2O5 gave pyrrolyl-substituted triazines.
引用
收藏
页码：1573 / 1577
页数：5
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