反应 #58178

ord-230f657d8e3d4a6a8770b3ebd44fd36b

反应方程式

Oc1cc(-c2ccccc2)nc(-c2ccc(Cl)cc2)n1
2-(4-chloro-phenyl)-6-phenyl-pyrimidin-4-ol
Oc1cc(-c2ccccc2)nc(-c2ccc(Cl)cc2)n1
Intermediate 1
Oc1cc(-c2ccccc2)nc(-c2ccc(Cl)cc2)n1
2-(4-chloro-phenyl)-6-phenyl-pyrimidin-4-ol
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
Fc1ccc(COc2cc(-c3ccccc3)nc(-c3ccc(Cl)cc3)n2)cc1
title compound
Fc1ccc(COc2cc(-c3ccccc3)nc(-c3ccc(Cl)cc3)n2)cc1
2-(4-Chlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-phenylpyrimidine

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared from 2-(4-chloro-phenyl)-6-phenyl-pyrimidin-4-ol (which was obtained in Intermediate 1) and 4-fluorobenzyl bromide according to Method A; LC retention time 4.35 min; MS: m/z (ESI) 391 (M+H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07423044B2uspto-grants-2008_09