反应 #58177

ord-427b996b8384497b91c8121c533f3034

反应方程式

Oc1nc(-c2ccccc2)nc2c1CCC2
2-phenyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ol
Oc1nc(-c2ccccc2)nc2c1CCC2
Intermediate 5
Oc1nc(-c2ccccc2)nc2c1CCC2
2-phenyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ol
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
Fc1ccc(COc2nc(-c3ccccc3)nc3c2CCC3)cc1
title compound
Fc1ccc(COc2nc(-c3ccccc3)nc3c2CCC3)cc1
4-[(4-Fluorobenzyl)oxy]-2-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared from 2-phenyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ol (which was obtained in Intermediate 5) and 4-fluorobenzyl bromide according to Method A; LC retention time 3.26 min; MS: m/z (ESI) 321 (M+H).

来源

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