HRID844894

反应详情

EQUATION

反应方程式

HRID 844894 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylaianine (1.0 mmol, 460 mg), 2-[(N,N-diethyl)aminolethyl chloride hydrochloride (8.05 mmol, 1.43 g) and potassium carbonate (8.05 mmol, 1.11 g) in ethyl acetate (5 mL) and water (5 mL) was stirred at room termperature overnight. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×40 mL). The combined extracts were washed with brine (50 mL) and dried over anhydrous sodium sulfate. Filtration of the drying agent and concentration of the filtrate gave the crude product which was purified by silica gel chromatography using a Biotage (40m) column to obtain 426 mg (76% yield) of N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine 2-[(N,N-diethyl)amino]ethyl ester as an amorphous white solid. ES-HRMS m/e calcd for C29H34F2N4O5 (M+H) 557.2570, found 557.2575.

WORKUP

后处理

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with ethyl acetate (2×40 mL)
  3. washThe combined extracts were washed with brine (50 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationFiltration of the drying agent and concentration of the filtrate
  6. customgave the crude product which
  7. customwas purified by silica gel chromatography