反应详情
EQUATION
反应方程式
REACTANTS
反应物
4-Methylmorpholine
C5H11NO
2 次
1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-
C10H17NO4
2 次
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
2 次
6-Bromoisoquinolin-1-amine
C9H7BrN2
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a mixture of 6-Bromo-isoquinolin-1-ylamine (0.80 g), Boc-L-proline (0.803 g), and 4-methylmorpholine (0.83 mL) in DMF (10 mL) was added HATU (1.39 g). Reaction mixture was stirred for 6 hours. Additional Boc-L-proline (0.803 g), 4-methylmorpholine (0.83 mL) and HATU (1.39 g) were added and reaction stirred overnight at ambient temperature and then concentrated. The residue was dissolved in ethyl acetate and washed with 10:1 H2O/saturated sodium bicarbonate solution, 5% lithium chloride solution, brine and dried (MgSO4), concentrated and purified by flash column chromatography (silica gel, 20 to 70% ethyl acetate/hexanes) to give 2-(6-Bromo-isoquinolin-1-yl carbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (1.74 g): LCMS-ESI+: calc'd for C19H23BrN3O3: 421.31 (M+H+). Found: 419.8, 421.8 (M+H+).
WORKUP
后处理
- customReaction mixture
- customreaction
- stirringstirred overnight at ambient temperature
- concentrationconcentrated
- dissolutionThe residue was dissolved in ethyl acetate
- washwashed with 10:1 H2O/saturated sodium bicarbonate solution, 5% lithium chloride solution, brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- custompurified by flash column chromatography (silica gel, 20 to 70% ethyl acetate/hexanes)