反应 #58176

ord-8a7e17ed8cb048fe99283bf591303c75

反应方程式

Oc1cc(-c2ccccc2)nc(-c2ccncc2)n1
6-phenyl-2-pyridin-4-yl-pyrimidin-4-ol
Oc1cc(-c2ccccc2)nc(-c2ccncc2)n1
Intermediate 3
Oc1cc(-c2ccccc2)nc(-c2ccncc2)n1
6-phenyl-2-pyridin-4-yl-pyrimidin-4-ol
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
Fc1ccc(COc2cc(-c3ccccc3)nc(-c3ccncc3)n2)cc1
title compound
Fc1ccc(COc2cc(-c3ccccc3)nc(-c3ccncc3)n2)cc1
4-[(4-Fluorobenzyl)oxy]-6-phenyl-2-pyridin-4-ylpyrimidine

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared from 6-phenyl-2-pyridin-4-yl-pyrimidin-4-ol (which was obtained in Intermediate 3) and 4-fluorobenzyl bromide according to Method A; 1H NMR (DMSO-d6, 300 MHz) δ 5.72 (s, 2H), 7.50-7.70 (m, 6H), 7.93 (d, J=15.0 Hz, 2H), 8.30-8.37 (m, 2H), 8.37-8.41 (m, 2H), 8.80-8.90 (m, 2H); LC retention time 3.02 min; MS: m/z (ESI) 358 (M+H).

来源

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