反应详情

The title compound was prepared by a procedure similar to that described for E1 starting from 4-{[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]oxy}-2(1H)-pyrimidinone and 4-(chloromethyl)pyridine hydrochloride. LC-MS (ESI): m/z 502 [M+H]+; 4.27 min (ret time).

1. custom4.27 min (ret time)