HRID1392238

反应详情

EQUATION

反应方程式

HRID 1392238 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of [4-(4-[1,2,3]Triazol-1-yl-butyl)-phenyl]-carbamic acid tert-butyl ester (0.297 g, 0.94 mmol) in N,N-dimethyl formamide (5 ml) sodium hydride (0.050 g, 2.1 mmol) was added and the mixture stirred for 30 min at r.t. To this mixture a solution of 2-(4-chloromethyl-oxazol-2-yl)-5-trifluoromethoxy-1H-indole 0.3 g, 0.94 mmol) in N,N-dimethyl formamide (5 ml) was added and stirring continued for 16 h. The mixture was then poured on water (25 ml) and extracted with ethyl acetate (3×25 ml). The combined organic extracts was washed with water, brine and dried over sodium sulfate. After concentration in vacuo the crude product was purified on silica gel (iso-hexanes/ethyl acetate 1:2) to yield [4-(4-[1,2,3]Triazol-1-yl-butyl)-phenyl]-[2-(5-trifluoromethoxy-1H-indol-2-yl)-oxazol-4-ylmethyl]-carbamic acid tert-butyl ester as light yellow solid.

WORKUP

后处理

  1. stirringstirring
  2. waitcontinued for 16 h
  3. additionThe mixture was then poured on water (25 ml)
  4. extractionextracted with ethyl acetate (3×25 ml)
  5. washThe combined organic extracts was washed with water, brine
  6. dry with materialdried over sodium sulfate
  7. concentrationAfter concentration in vacuo the crude product
  8. customwas purified on silica gel (iso-hexanes/ethyl acetate 1:2)