反应 #1726703

ord-37143c90f5964c4bb78a2c7b3c36423d

反应方程式

O=C([O-])O.[Na+]
sodium bicarbonate
Cl.N#CC(N)c1ccccc1
α-aminophenylacetonitrile hydrochloride
O=C(N=C=S)OCC1c2ccccc2-c2ccccc21
Fmoc-isothiocyanate
CCN(C(C)C)C(C)C
ethyldiisopropylamine
Nc1sc(NC(=O)OCC2c3ccccc3-c3ccccc32)nc1-c1ccccc1
5-amino-2-(Fmoc-amino)-4-phenylthiazole
收率 48.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted three times into ethyl acetate
  2. 2
    洗涤The combined organic phases were washed with water and brine
  3. 3
    干燥dried over sodium sulfate
  4. 4
    浓缩concentrated in vacuo

实验过程

A suspension of α-aminophenylacetonitrile hydrochloride (3.19 g, 18.9 mmol) and Fmoc-isothiocyanate (5.31 g, 18.9 mmol) in DCM was treated with ethyldiisopropylamine (3.62 ml, 20.8 mmol) at 0° C. for 1 hr and then at ambient temperature for 3 hr. The mixture was poured into saturated aqueous sodium bicarbonate and extracted three times into ethyl acetate. The combined organic phases were washed with water and brine, and dried over sodium sulfate and concentrated in vacuo. Flash chromatography on silica gel (ethyl acetate/hexanes) yielded 5-amino-2-(Fmoc-amino)-4-phenylthiazole (3.75 g, 48%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08110568B2uspto-grants-2012_02