反应详情

A solution of 2-methyl-4-{[3-methyl-1-(2-methyl-5-phenylfuran-3-yl)butyl]amino}benzoic acid (228 mg), ethyl 3-(methylamino)propanoate (94 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (138 mg), hydroxybenzotriazole monohydrate (110 mg) and triethylamine (100 μL) in N,N-dimethylformamide (10 mL) was stirred at room temperature for 4 hr. Ethyl acetate was added, the mixture was washed with saturated aqueous sodium hydrogen carbonate solution and water, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure. To the residue were added ethanol (2 mL), tetrahydrofuran (2 mL) and 1N lithium hydroxide (1.2 mL), and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure, and water (10 mL) was added. The mixture was neutralized with 1N hydrochloric acid under ice-cooling, and stirred for 1 hr. The resulting precipitate was collected by filtration and dried to give the title compound (271 mg, 97%).

1. washthe mixture was washed with saturated aqueous sodium hydrogen carbonate solution and water
2. dry with materialthe organic layer was dried over magnesium sulfate
3. customThe solvent was evaporated under reduced pressure
4. dry with materialthe organic layer was dried over magnesium sulfate
5. customThe solvent was evaporated under reduced pressure
6. additionTo the residue were added ethanol (2 mL), tetrahydrofuran (2 mL) and 1N lithium hydroxide (1.2 mL)
7. customThe solvent was evaporated under reduced pressure, and water (10 mL)
8. additionwas added
9. temperaturecooling
10. stirringstirred for 1 hr
11. filtrationThe resulting precipitate was collected by filtration
12. customdried