反应详情

The title compound was prepared by a procedure similar to that described for E1 starting from 4-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]oxy}-2(1H)-pyrimidinone and 4-(chloromethyl)-1-methyl-1H-pyrazole hydrochloride. LC-MS (ESI): m/z 491 [M+H]+; 3.49 min (ret time).

1. custom3.49 min (ret time)