反应详情

The title compound was prepared by a procedure similar to that described for E1 starting from 6-{[2-(5-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}-2-pyridinyl)ethyl]oxy}-2(1H)-pyrimidinone and 4-(chloromethyl)-1-methyl-1H-pyrazole hydrochloride. LC-MS (ESI): m/z 506 [M+H]+; 2.90 min (ret time).

1. custom2.90 min (ret time)