反应 #1095865

ord-f3b780e9ae414faa8dc4726136e57c52

反应方程式

C1CCNCC1
piperidine
CN(C)C=O
N,N-dimethylformamide
CC#CCOc1cc(Cl)ncn1
4-chloro-6-(2-butynyloxy)pyrimidine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC#CCOc1cc(N2CCCCC2)ncn1
4-(2-butynyloxy)-6-piperidinopyrimidine
收率 77.1%

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    温度The reaction mixture was cooled to near room temperature
  3. 3
    洗涤the mixture was washed with a saturated sodium chloride aqueous solution three times
  4. 4
    干燥The organic layers were dried over anhydrous magnesium sulfate
  5. 5
    浓缩concentrated

实验过程

Into 2 ml of N,N-dimethylformamide was resolved 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate and 85 mg of piperidine was added therein, and the mixture was stirred for 5 hours at 80° C. The reaction mixture was cooled to near room temperature, ethyl acetate was added therein, and the mixture was washed with a saturated sodium chloride aqueous solution three times. The organic layers were dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 178 mg of 4-(2-butynyloxy)-6-piperidinopyrimidine (hereinafter, referred to as Compound (16)).

来源

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