HRID1372202

反应详情

EQUATION

反应方程式

HRID 1372202 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
25 °C

PROCEDURE

实验过程

A solution of intermediate 6, ethyl 3-(benzyloxy)-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylate (0.300 g, 0.91 mmol) in ethanol (10 ml) was treated with 3 ml (3.0 mmol) of 1 N sodium hydroxide and stirred at 25° C. for 30 min. The solution was then acidified with 1 N hydrochloric acid, extracted with ethyl acetate, washed with brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave 0.264 g (96% yield) of the title acid as white crystals; mp 171° C. (ethyl acetate). 1HNMR 400 MHz (CDCl3) δ (ppm): 4.03 (2H, t, J=5.3 Hz, CH2), 4.12 (2H, t, J=5.3 Hz, CH2), 4.73 (2H, s, OCH2), 5.53 (2H, s, OCH2), 7.35–7.42 (3H, m, aromatics), 7.53 (2H, m, aromatics). Anal. Calcd for C15H14N2O5: C, 59.60; H, 4.67; N, 9.27. Found: C, 59.35; H, 4.69; N, 9.10.

WORKUP

后处理

  1. extractionextracted with ethyl acetate
  2. washwashed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customEvaporation of the solvent
  5. customgave 0.264 g (96% yield) of the title acid as white crystals