反应详情

温度

0 °C

N-tert-butoxycarbonyl-D-valine (5.34 g, 24.6 mmols) and 5.31 g (24.6 mmols) of (RS)-α-methoxycarbonylmethylbenzylamine hydrochloride (S:R=2:1) were suspended in 100 ml of methylene chloride, and the suspension was maintained at 0° C. Triethylamine (3.78 ml, 27.1 mmols), 5.20 g (27.1 mmols) of water-soluble carbodiimide hydrochloride and 3.66 g (27.1 mmols) of HOBt were added thereto, and the mixture was stirred for 1 hour while being cooled and then overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and 150 ml of water were then added to the residue. The solution was extracted twice with 100 ml of ethyl acetate. The organic layer was washed twice with 100 ml of a 5% citric acid aqueous solution, with 100 ml of a saturated aqueous solution of sodium chloride, twice with a 5% sodium hydrogencarbonate aqueous solution and with 100 ml of a saturated aqueous solution of sodium chloride. The organic layer was dried over anhydrous magnesium sulfate, and magnesium sulfate was then removed by filtration. The filtrate was concentrated under reduced pressure to obtain 9.27 g (24.5 mmols) of N-tert-butoxycarbonyl-D-valine (RS)-α-methoxycarbonylmethylbenzylamide as a solid.

1. temperaturewhile being cooled
2. customovernight
3. customat room temperature
4. concentrationThe reaction mixture was concentrated under reduced pressure, and 150 ml of water
5. additionwere then added to the residue
6. extractionThe solution was extracted twice with 100 ml of ethyl acetate
7. washThe organic layer was washed twice with 100 ml of a 5% citric acid aqueous solution, with 100 ml of a saturated aqueous solution of sodium chloride, twice with a 5% sodium hydrogencarbonate aqueous solution and with 100 ml of a saturated aqueous solution of sodium chloride
8. dry with materialThe organic layer was dried over anhydrous magnesium sulfate, and magnesium sulfate
9. customwas then removed by filtration
10. concentrationThe filtrate was concentrated under reduced pressure