HRID486506

反应详情

EQUATION

反应方程式

HRID 486506 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a suspension of 1.75 g of ethyl 3-(2-butyl-1,4-dihydro-4-oxo-6-quinazolinyl)-2-propenoate in 25 ml of dry tetrahydrofuran at room temperature is rapidly added 6.70 g of a 1.0M solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran. After stirring for 20 minutes at room temperature 3.899 g of 5-(4'-(bromomethyl)-[1,1'-biphenyl]-2-yl]-1-(triphenylmethyl)-1H-tetrazole is rapidly added in one portion and the reaction mixture heated at reflux for 48 hours. After cooling to room temperature, the reaction mixture is diluted with ethyl acetate and the organic layer washed with 5% HCl, water and brine. The organic layer is dried with MgSO4 and concentrated in vacuo to a residue which is purified by column chromatography on silicagel by eluting with 1:4 ethyl acetate-hexanes to give 1.732 g of the desired product as a solid. FAB MASS SPEC 799 (M+Na)

WORKUP

后处理

  1. additionis rapidly added in one portion
  2. temperaturethe reaction mixture heated
  3. temperatureat reflux for 48 hours
  4. washthe organic layer washed with 5% HCl, water and brine
  5. dry with materialThe organic layer is dried with MgSO4
  6. concentrationconcentrated in vacuo to a residue which
  7. customis purified by column chromatography on silicagel
  8. washby eluting with 1:4 ethyl acetate-hexanes