2,2,2-Trifluoroethanol → HCID 68108403、化合物
反応式
[F:1][C:2]([F:6])([F:5])[CH2:3][OH:4].C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:13][O:14][C:15]([C:17]1[C:22]([NH2:23])=[N:21][C:20](Cl)=[CH:19][N:18]=1)=[O:16].[NH4+].[Cl-]>>[CH3:13][O:14][C:15]([C:17]1[C:22]([NH2:23])=[N:21][C:20]([O:4][CH2:3][C:2]([F:6])([F:5])[F:1])=[CH:19][N:18]=1)=[O:16]参加物
5
実験手順
A mixture of 2,2,2-trifluoro-ethanol (6.9 ml, 96 mmol) and cesium carbonate (1.56 g, 4.8 mmol) was stirred for 20 min, 3-amino-5-chloro-pyrazine-2-carboxylic acid methyl ester [28643-16-5] (600 mg, 3.2 mmol) was added and the mixture was stirred at rt for 42 h. To complete the reaction the mixture was heated to reflux for another 3 h. Saturated aq. NH4Cl was added and the mixture was extracted with EtOAc, the combined organic layers were washed with saturated aq. sodium chloride, dried with Na2SO4 and evaporated. The residue was purified by chromatography on silica gel (cyclohexane to cyclohexane/EtOAc 3:7) to provide the title compound as colorless solid.