Реакция #3019

Уравнение реакции

2,6-dimethoxy-4-methylaniline hydrochloride

N-Boc-glycine

BOP

dimethylformamide

→

N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine

Выход 96.0%

Растворители

ethyl acetate

triethylamine

diisopropyl ether

Условия реакции

Обработка

1. 1
   workup.WAITThe reaction mixture is left at room temperature for 15 hours
2. 2
   Промывкаthe organic phase is successively washed with 3×200 ml of water, with a 1N aqueous sodium hydroxide solution
3. 3
   СушкаThe organic phase is dried over anhydrous sodium sulphate
4. 4
   ДругоеEvaporation of the solvent
5. 5
   Другоеleaves a semi-crystalline residue which

Методика

6.6 g of N-Boc-glycine and 15.6 g of BOP are successively added to 100 ml of dimethylformamide and then, at 0° C., 14 ml of triethylamine are added dropwise. The mixture is left for 20 minutes at 0° C. and 6.7 g of 2,6-dimethoxy-4-methylaniline hydrochloride are then added portionwise. The reaction mixture is left at room temperature for 15 hours. 400 ml of ethyl acetate are added to the reaction mixture and the organic phase is successively washed with 3×200 ml of water, with a 1N aqueous sodium hydroxide solution and then with water. The organic phase is dried over anhydrous sodium sulphate. Evaporation of the solvent leaves a semi-crystalline residue which is solidified in diisopropyl ether to provide N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine, in the form of white crystals; M.p.=146° C.; Yield: 96%.

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