تفاعل #318111
ord-98c61b32b2014508951e69474095d4ab
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1استخلاصthe resulting mixture was extracted with ethyl acetate
- 2غسيلThe extract was washed with water, 1 mol/L aqueous sodium hydroxide solution, water and brine successively
- 3تجفيفdried over anhydrous sodium sulfate
- 4أخرىThe solvent was removed under reduced pressure
- 5workup.ADDITIONTo the residue was added 4 mol/L hydrochloric acid (1,4-dioxane solution, 25 mL)
- 6workup.STIRRINGthe mixture was stirred at room temperature for 4 hours
- 7workup.ADDITIONTo the reaction mixture was added diethyl ether (50 mL)
- 8ترشيحthe insoluble material was collected by filtration
- 9غسيلThe collected solid was washed with diethyl ether
- 10أخرىdried under reduced pressure
الإجراء التجريبي
To a solution of 2-(tert-butoxycarbonylamino)-2-methylpropionate (4.06 g) in N,N-dimethylformamide (40 mL) were added 1-(benzyloxycarbonyl)piperazine (6.6 g), 1-hydroxybenzotriazole (3.24 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (7.67 g) and triethylamine (11.2 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water, 1 mol/L aqueous sodium hydroxide solution, water and brine successively, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. To the residue was added 4 mol/L hydrochloric acid (1,4-dioxane solution, 25 mL), and the mixture was stirred at room temperature for 4 hours. To the reaction mixture was added diethyl ether (50 mL), and the insoluble material was collected by filtration. The collected solid was washed with diethyl ether and dried under reduced pressure to give the title compound (4.65 g).