反応 #58181

ord-564c311f8b8340389fe9e122cf634a45

反応方程式

CC(C)c1cc(O)nc(-c2cc(Cl)cc(Cl)c2)n1
2-(3,5-dichloro-phenyl)-6-isopropyl-pyrimidin-4-ol
CC(C)c1cc(O)nc(-c2cc(Cl)cc(Cl)c2)n1
Intermediate 6
CC(C)c1cc(O)nc(-c2cc(Cl)cc(Cl)c2)n1
2-(3,5-dichloro-phenyl)-6-isopropyl-pyrimidin-4-ol
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
CC(C)c1cc(OCc2ccc(F)cc2)nc(-c2cc(Cl)cc(Cl)c2)n1
title compound
CC(C)c1cc(OCc2ccc(F)cc2)nc(-c2cc(Cl)cc(Cl)c2)n1
2-(3,5-Dichlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-isopropylpyrimidine

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

The title compound was prepared from 2-(3,5-dichloro-phenyl)-6-isopropyl-pyrimidin-4-ol (which was obtained in Intermediate 6) and 4-fluorobenzyl bromide according to Method A; 1H NMR (DMSO-d6, 300 MHz) δ 1.27 (d, J=6.8 Hz, 6H), 2.90-3.10 (m, 1H), 5.54 (s, 2H), 6.88 (s, 1H), 7.24 (t, J=8.9 Hz, 2H), 7.57 (d, J=8.9, 8.5 Hz, 2H), 7.81 (s, 1H), 8.33 (s, 2H); LC retention time 4.45 min; MS: m/z (ESI) 391 (M+H).

出典

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