Ureas in Organic Synthesis. XII. Syntesis of 2-Amino-5-chlorobenzhydrylureas and their heterocyclization

Bibliographic Details
Parent link:Russian Journal of Organic Chemistry.— , 1997
Vol. 33, № 4.— 1997.— P. 457-459
Main Author: Bakibaev A. A. Abdigali Abdimanapovich
Other Authors: Shtrykova В. В., Vostretsov S. N.
Summary:A synthetic method was developed for hard-to-get biologically active 2-amino-5-chlorobenzhydrylureasbased on reaction of the corresponding benzhydrols with urea in sulfuric acid. The 2-amino-5-chlorobenzhydrylureas were shown to easily undergo on heating cyclization to 1-R-1,2,3,4-tetrahydro-4-phenyl-chloroquinazolin-2-ones.
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Published: 1997
Subjects:
Format: Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=596553
Description
Summary:A synthetic method was developed for hard-to-get biologically active 2-amino-5-chlorobenzhydrylureasbased on reaction of the corresponding benzhydrols with urea in sulfuric acid. The 2-amino-5-chlorobenzhydrylureas were shown to easily undergo on heating cyclization to 1-R-1,2,3,4-tetrahydro-4-phenyl-chloroquinazolin-2-ones.
В фонде НТБ ТПУ отсутствует