反应详情
EQUATION
反应方程式
REACTANTS
反应物
Sodium Bicarbonate
CHNaO3
Potassium acetate
C2H3KO2
Bis(pinacolato)diboron
C12H24B2O4
tert-Butyl 6-[(trifluoromethanesulfonyl)oxy]-3,4-dihydroisoquinoline-2(1H)-carboxylate
C15H18F3NO5S
5-Bromo-2-cyclopropylpyrimidine
C7H7BrN2
Potassium phosphate, tribasic, monohydrate
H2K3O5P
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 90 °C
PROCEDURE
实验过程
6-Trifluoromethanesulfonyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (11.51 g, 30 mmol) was dissolved in DMF (250 mL) and the yellow solution was purged by bubbling argon (g) through the solution. Potassium acetate (8.83 g, 90 mmol), bis(pinacolato)diboron (8.38 g, 33 mmol), PdCl2 dppf (1.22 g, 1.5 mmol) and dppf (0.83 g, 1.5 mmol) were added and the mixture was purged again with argon. The mixture was then heated to 90° C. for 2 h. Tripotassium phosphate monohydrate (18 g, 78 mmol) was added followed by 2-cyclopropyl-5-bromo-pyrimidine (7.76 g, 39 mmol) and stirring was continued for 5 h at 90° C. The reaction mixture was poured onto saturated sodium bicarbonate solution and extracted several times with ethyl acetate. The ethyl acetate solution was dried over magnesium sulphate, the drying agent filtered off and the filtrate was evaporated. The residue was purified by flash chromatography eluting with ethyl acetate:heptane (1:3) to give 8.1 g (76%) of the title compound as a colourless solid.
WORKUP
后处理
- customthe yellow solution was purged
- customby bubbling argon (g) through the solution
- customthe mixture was purged again with argon
- extractionextracted several times with ethyl acetate
- dry with materialThe ethyl acetate solution was dried over magnesium sulphate
- filtrationthe drying agent filtered off
- customthe filtrate was evaporated
- customThe residue was purified by flash chromatography
- washeluting with ethyl acetate:heptane (1:3)