反応式
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([F:11])([F:10])[F:9])=[N:6][CH:7]=1.Cl[C:13]1[CH:18]=[N:17][CH:16]=[CH:15][N:14]=1>C1(C)C=CC=CC=1>[N:14]1[CH:15]=[CH:16][N:17]=[CH:18][C:13]=1[NH:1][C:2]1[CH:7]=[N:6][C:5]([C:8]([F:11])([F:9])[F:10])=[CH:4][CH:3]=1参加物
4
反応条件
- 温度
- 95 °C
実験手順
To a solution of 5-amino-2-trifluoromethylpyridine (0.81 g) in 3 Ml toluene was added chloropyrazine (0.45 Ml, 1.0 equiv) via syringe. The homogeneous solution was heated to 95° C., then cooled to room temperature and concentrated in vacuo. Purification by silica gel chromatography (40% EtOAc in hexanes) afforded the title compound: 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 7.5 (s, 1H) 7.6 (s, 1H) 8.0 (s, 1H) 8.2 (s, 1H) 8.4 (s, 2H) 8.8 (s, 1H); (M+H)+241.1.
後処理
- temperaturecooled to room temperature
- concentrationconcentrated in vacuo
- customPurification by silica gel chromatography (40% EtOAc in hexanes)
出典と根拠
- ORDレコード
- ord-05ccb44a87384efd87e49f2df85e767d
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08835451B2
関連ノート
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