反応 #1726703

ord-37143c90f5964c4bb78a2c7b3c36423d

反応方程式

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
収率 48.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted three times into ethyl acetate
  2. 2
    洗浄The combined organic phases were washed with water and brine
  3. 3
    乾燥dried over sodium sulfate
  4. 4
    濃縮concentrated in vacuo

実験手順

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%).

出典

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