反应详情
EQUATION
反应方程式
REACTANTS
反应物
Triethylamine
C6H15N
Cyanoacetic acid
C3H3NO2
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
N4-(9-azaspiro[5.5]undecan-3-yl)-5-chloro-N2-(2,3-dimethylindazol-6-yl)pyrimidine-2,4-diamine
C23H30ClN7
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of 5-chloro-N2-(2,3-dimethyl-2H-indazol-6-yl)-N4-(3-azaspiro[5.5]undecan-9-yl)pyrimidine-2,4-diamine (485.3 mg, 1.10 mmol) and 2-cyanoacetic acid (137.0 mg, 1.61 mmol) in a mixture of DCM (40 mL) and DMF (10 mL) were added HATU (520.8 mg, 1.37 mmol) and Et3N (0.36 g, 3.55 mmol). After addition, the reaction mixture was stirred at rt for 6 h, then quenched with H2O (30 mL) and extracted with DCM (100 mL×3). The combined organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4, concentrated in vacuo. The residue was purified by silica gel column chromatography (MeOH/DCM (v/v)=1/50) to give the title compound as a beige solid (171.0 mg, 30.6%).
WORKUP
后处理
- additionAfter addition
- customquenched with H2O (30 mL)
- extractionextracted with DCM (100 mL×3)
- washThe combined organic phases were washed with brine (100 mL)
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel column chromatography (MeOH/DCM (v/v)=1/50)