反应 #1095873

ord-fdf92ab7964b4e9a82d13494eee4ee19

反应方程式

CC#CCOc1cc(Cl)ncn1
4-chloro-6-(2-butynyloxy)pyrimidine
FC(F)(F)C1CCCNC1
3-trifluoromethylpiperidine
CC#CCOc1cc(N2CCCC(C(F)(F)F)C2)ncn1
4-(2-butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine
收率 61.4%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

0.3 g of 4-chloro-6-(2-butynyloxy)pyrimidine and 0.25 g of 3-trifluoromethylpiperidine were mixed and left for 10 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.30 g of 4-(2-butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine (hereinafter, referred to as Compound (24)).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07973028B2uspto-grants-2011_07