反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydrochloric Acid
ClH
N,N-Dimethylformamide
C3H7NO
Benzoic acid, 4-amino-3-fluoro-
C7H6FNO2
Diisopropylethylamine
C8H19N
1-[1-(4-chlorophenyl)cyclopropyl]methanamine
C10H12ClN
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
PRODUCTS
生成物
PROCEDURE
实验过程
To a mixture of 4-amino-3-fluorobenzoic acid (180.0 mg, 1.160 mmol) and N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (HATU, 0.44 g, 1.2 mmol) in N,N-dimethylformamide (2 mL, 20 mmol) at 0° C. were added N,N-diisopropylethylamine (0.61 mL, 3.5 mmol) and C-[1-(4-chloro-phenyl)-cyclopropyl]-methylamine; hydrochloride (303.7 mg, 1.392 mmol). The reaction mixture was slowly warmed to rt. The reaction mixture was quenched with an equal volume of saturated aqueous sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic layers were washed successively with water, aqueous lithium chloride, and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on the Isco (120 g cartridge, chloroform to 12% methanol in chloroform).
WORKUP
后处理
- customThe reaction mixture was quenched with an equal volume of saturated aqueous sodium bicarbonate
- extractionextracted with ethyl acetate (3×)
- washThe combined organic layers were washed successively with water, aqueous lithium chloride, and brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified on the Isco (120 g cartridge, chloroform to 12% methanol in chloroform)