反应详情
EQUATION
反应方程式
REACTANTS
反应物
N,N-Dimethylformamide
C3H7NO
Diisopropylethylamine
C8H19N
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
(R)-(+)-3-Aminoquinuclidine dihydrochloride
C7H16Cl2N2
6-Nitro-1-benzofuran-2-carboxylic acid
C9H5NO5
PRODUCTS
生成物
PROCEDURE
实验过程
1040 mg (5.02 mmol) of 6-nitrobenzofuran-2-carboxylic acid, 1000 mg (5.02 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 2290 mg (6.03 mmol) of HATU, 2250 mg (18.08 mmol) of N,N-diisopropylethylamine and 9 ml of DMF are reacted according to the general procedure (variant B). DMF is removed under reduced pressure. The product is taken up in 100 ml of 1N aqueous sodium hydroxide solution and extracted three times with in each case 50 ml of ethyl acetate. The combined organic phases are washed eight times with 1N aqueous sodium hydroxide solution and once with saturated sodium chloride solution and then dried over magnesium sulfate, and the solvent is removed under reduced pressure using a rotary evaporator. 1.34 g (79% of theory) of the title compound are obtained.
WORKUP
后处理
- customDMF is removed under reduced pressure
- extractionextracted three times with in each case 50 ml of ethyl acetate
- washThe combined organic phases are washed eight times with 1N aqueous sodium hydroxide solution
- dry with materialonce with saturated sodium chloride solution and then dried over magnesium sulfate
- customthe solvent is removed under reduced pressure
- customa rotary evaporator