反応 #43379

ord-85ce16b4205a42c8bd3450e8ff110de5

反応方程式

O=C(O)c1ccc(Br)s1
5-bromo-thiophene-2-carboxylic acid
O=S(Cl)Cl
thionyl chloride
CC(C)(C)OC(=O)C(C)(C)N.Cl
tert.-butyl 2-amino-isobutyrate hydrochloride
O
water
CC(C)(C)OC(=O)C(C)(C)NC(=O)c1ccc(Br)s1
tert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The mixture is then evaporated down i
  2. 2
    その他evaporated down completely
  3. 3
    workup.ADDITIONThe residue is added dropwise to 10 ml dichloromethane
  4. 4
    workup.STIRRINGstirred for 16 h
  5. 5
    抽出extracted with dichloromethane
  6. 6
    乾燥the combined organic phases are dried over magnesium sulphate
  7. 7
    その他evaporated down i

実験手順

2.63 g (12.3 mmol) 5-bromo-thiophene-2-carboxylic acid are refluxed in 15 ml dichloromethane together with 7.0 ml of thionyl chloride for 2 h with stirring. The mixture is then evaporated down i. vac. and the residue is twice taken up in toluene and evaporated down completely i. vac. The residue is added dropwise to 10 ml dichloromethane with stirring at ambient temperature in a mixture of 2.41 g (12.3 mmol) tert.-butyl 2-amino-isobutyrate hydrochloride in 20 ml dichloromethane with 5.14 ml (36.9 mmol) TEA and stirred for 16 h. The mixture is poured into water and extracted with dichloromethane, the combined organic phases are dried over magnesium sulphate and evaporated down i. vac.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07732466B2uspto-grants-2010_06