反应 #42791

ord-128a683dc56a4a128028ba8b3f713edc

反应方程式

CC#CCOc1ncnc(Cl)c1F
4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine
CC1CCCCN1
2-methylpyperidine
CC#CCOc1ncnc(N2CCCCC2C)c1F
4-(2-butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine
收率 71.1%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    温度under reflux condition
  3. 3
    浓缩concentrated

实验过程

Into 3 ml of ethanol was resolved 0.3 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.45 g of 2-methylpyperidine was added therein, and the mixture was stirred for 5 hours under reflux condition. The reaction mixture was cooled to near room temperature and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.28 g of 4-(2-butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine (hereinafter, referred to as Compound (1)).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07732448B2uspto-grants-2010_06