反应 #1095861
ord-916e6a2e10f4452bbeb81b31fa1b44cc
反应方程式
4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine
3,5-dimethylpiperidine
→
4-(3,5-dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine
收率 84.7%
反应条件
详细条件
See reaction.notes.procedure_details.
实验过程
0.2 g of 4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine and 0.32 g of 3,5-dimethylpiperidine (cis/trans=about 3/1) were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.23 g of 4-(3,5-dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine (hereinafter, referred to as Compound (11)). Compound (11) had the cis/trans diastereomer originated two methyls on the piperidine ring. The ratio of the cis/trans diastereomer was about 3.8/1.