反应详情

A stirred solution of 8 g of 2-amino-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine in 40 ml of N,N-dimethylformamide was treated with a solution of 6.41 g of N-chlorosuccinimide in 40 ml of N,N-dimethylformamide and then stirred at room temperature for 8 hours. Evaporation of the volatiles afforded an oil which was decanted into 100 ml of water, basified with 30 ml of 10% aqueous sodium hydroxide and extracted with dichloromethane (2×100 ml). The extract was washed with water (2×100 ml), dried over anhydrous sodium sulfate and concentrated. Thin layer chromatography of the resultant oil indicated a multicomponent mixture. Purification of the mixture was accomplished by successive HPLC separations (Water's Associates Prep LC/System 500, silica gel, elution with methanol). Concentration of the appropriate fractions afforded a residue which was dissolved in diethyl ether, filtered free of insolubles and concentrated. The resultant oil crystallized upon standing to yield 1.05 g of 2-amino-5-chloro-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine, mp 59°-61° C.

1. customEvaporation of the volatiles
2. customafforded an oil which
3. customwas decanted into 100 ml of water
4. extractionextracted with dichloromethane (2×100 ml)
5. washThe extract was washed with water (2×100 ml)
6. dry with materialdried over anhydrous sodium sulfate
7. concentrationconcentrated
8. customPurification of the mixture
9. washwas accomplished by successive HPLC separations (Water's Associates Prep LC/System 500, silica gel, elution with methanol)
10. customConcentration of the appropriate fractions afforded a residue which
11. filtrationfiltered free of insolubles
12. concentrationconcentrated
13. customThe resultant oil crystallized