反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
1-Methylindole-3-propionic acid (1.2 g, 6.0 mmole), 1-hydroxybenzotriazole hydrate (0.97 g, 7.2 mmole) and 1,3-diisopropylcarbodiimide (1.1 ml, 7.2 mmole) were combined in 100 ml of DMF and stirred at room temperature for 2 hours under a nitrogen atmosphere. To this was added dropwise 7-methylsulfonylamino-2,3-dihydro-1,4-benzodioxin-2-methanamine (1.9 g, 7.2 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and the residue partitioned between dichloromethane and water. The separated dichloromethane layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The residue was chromatographed on a silica gel column using ethyl acetate as the eluant. Fractions containing product were concentrated and washed with a minimum amount of THF to remove a by-product and to give 2.1 g (79%) of the desired product, (7-methylsulfonyl-2,3-dihydro-benzo[1,4]dioxin-2ylmethyl)-4-(1-methyl-1H-indol-3-yl)-propanamide, as a fluffy white solid.
WORKUP
后处理
- stirringthe mixture was further stirred for 24 hours
- customThe solvent was removed
- customthe residue partitioned between dichloromethane and water
- dry with materialThe separated dichloromethane layer was dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuum
- customThe residue was chromatographed on a silica gel column
- additionFractions containing product
- concentrationwere concentrated
- washwashed with a minimum amount of THF
- customto remove a by-product