HRID226986

反应详情

EQUATION

反应方程式

HRID 226986 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

25.6 mL of potassium hexamethyldisilazane (12.91 mmol, 0.5 M in tolene) was added to 2.5 g (10.76 mmol) of 7-Methyl-4-oxo-1,4-dihydro-[1,8]naphthyridine-3-carboxylic acid ethyl ester dissolved in 22 mL of tetrahydrofuran and was stirred at room temperature for 15 minutes. 3.24 g (12.91 mmol) of 2-Bromo-6-bromomethyl-pyridine was added and stirred at room temperature for 2.5 h. Water and ethyl acetate were added and the layers separated. The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over magnesium sulfate, filtered and dried in vacuo. The crude product was purified on silica gel eluting with 50/50 ethyl acetate/hexane to yield 0.620 g of 1-(6-Bromo-pyridin-2-ylmethyl)-7-methyl-4-oxo-1,4-dihydro-[1,8]naphthyridine-3-carboxylic acid ethyl ester as a brown solid.

WORKUP

后处理

  1. stirringstirred at room temperature for 2.5 h
  2. customthe layers separated
  3. extractionThe aqueous layer was extracted with ethyl acetate (3×50 mL)
  4. dry with materialThe combined organic layers were dried over magnesium sulfate
  5. filtrationfiltered
  6. customdried in vacuo
  7. customThe crude product was purified on silica gel eluting with 50/50 ethyl acetate/hexane