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
A solution of 5-(2-morpholinoethylaminosulphonyl)oxindole (364 mg, 1.1 mmol), (prepared as described for the starting material in Example 48), in DMF (3.5 ml) was added dropwise to a suspension of sodium hydride (90 mg, 2.2 mmol, prewashed with hexane) in DMF (1.5 ml). The mixture was stirred for 30 minutes at ambient temperature and 4-chloro-6,7dimethoxyquinazoline (84 mg, 0.37 mmol), (prepared as described for the starting material in Example 1), was added as a solid followed by DMSO (2 ml). The mixture was stirred for 45 minutes at 60° C., allowed to cool and partitioned between methylene chloride and saturated aqueous ammonium chloride solution. The organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5 followed by 92/8). The purified solid was triturated with ether, collected by filtration; washed with ether and dried under vacuum. The solid was dissolved in methylene chloride/methanol and 2M ethereal hydrogen chloride (1 ml) was added. The volatiles were removed bv evaporation, the solid residue triturated with ether, collected by filtration, washed with ether and dried under vacuum to give 6,7-dimethoxy-4-(5-(2-morpholinoethylaminosulphonyl)oxindol-3-yl)quinazoline hydrochloride (106 mg, 50%).
WORKUP
后处理
- additionwas added as a solid
- stirringThe mixture was stirred for 45 minutes at 60° C.
- temperatureto cool
- custompartitioned between methylene chloride and saturated aqueous ammonium chloride solution
- customThe organic layer was separated
- washwashed with brine
- dry with materialdried (MgSO4)
- customthe solvent removed by evaporation
- customThe residue was purified by column chromatography
- washeluting with methylene chloride/methanol (95/5 followed by 92/8)
- customThe purified solid was triturated with ether
- filtrationcollected by filtration
- washwashed with ether
- customdried under vacuum
- dissolutionThe solid was dissolved in methylene chloride/methanol
- addition2M ethereal hydrogen chloride (1 ml) was added
- customThe volatiles were removed
- custombv evaporation
- customthe solid residue triturated with ether
- filtrationcollected by filtration
- washwashed with ether
- customdried under vacuum