反应详情
EQUATION
反应方程式
REACTANTS
反应物
Citric Acid
C6H8O7
Diisopropylethylamine
C8H19N
2-(4-Methyl-piperidin-1-yl)-pyrimidine-5-carboxylic acid
C11H15N3O2
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
2-(Trifluoromethyl)-1H-indole-5-methanamine
C10H9F3N2
2 次
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a stirred solution of HATU (34.4 mg, 0.090 mmol) in 1 ml DMF was added (2-(4-methyl-1-piperidinyl)-5-pyrimidinecarboxylic acid) (Matrix Scientific, 20 mg, 0.090 mmol) in 0.5 ml DMF, followed by DIPEA (0.016 ml, 0.090 mmol) and finally {[2-(trifluoromethyl)-1H-indol-5-yl]methyl}amine (Intermediate 4, 22.66 mg, 0.090 mmol) in 1 ml DMF. Stirring was continued for 16 hours. 1M citric acid solution (10 ml) was added and the mixture was then extracted with ethyl acetate (20 ml). The organic extract was then washed with 1M citric acid solution (10 ml), brine (10 ml), dried (MgSO4), filtered and evaporated to dryness. The resulting residues where then purified on the MDAP to dryness to give the title compound (19 mg);
WORKUP
后处理
- extractionthe mixture was then extracted with ethyl acetate (20 ml)
- extractionThe organic extract
- washwas then washed with 1M citric acid solution (10 ml), brine (10 ml)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated to dryness
- customThe resulting residues where then purified on the MDAP to dryness