1,1'-Thiocarbonyldi-2(1H)-pyridone → 2,3-Dichloro-6-isothiocyanatopyridine
反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH2:9])=[N:6][C:7]=1[Cl:8].[C:10](N1C=CC=CC1=O)(N1C=CC=CC1=O)=[S:11]>ClCCl.C(OCC)(=O)C.CCCCCC>[Cl:8][C:7]1[C:2]([Cl:1])=[CH:3][CH:4]=[C:5]([N:9]=[C:10]=[S:11])[N:6]=1参加物
5
反応条件
- 温度
- 40 °C
実験手順
To 5,6-dichloropyridin-2-amine (0.47 g, 2.88 mmol) in dichloromethane (25 mL) was added 1,1′-thiocarbonyldipyridin-2(1 H)-one (0.68 g, 2.94 mmol). The reaction was stirred at 40° C. for 3 hours, then cooled to room temperature. The crude material was purified by chromatography (Biotage: 25-100% ethyl acetate/hexane) 2,3-dichloro-6-isothiocyanatopyridine (0.48 g, 2.34 mmol, 81% yield) as a white powder. 1H NMR (500 MHz, DMSO-D6) δ ppm 8.26 (d, J=8.55 Hz, 1 H), 7.47 (d, J=8.24 Hz, 1 H). MS (LC/MS) R.T.=2.83; [M+H]+=204.8.
後処理
- temperaturecooled to room temperature
出典と根拠
- ORDレコード
- ord-82566d13a2a149e88352ff9a8cf229d2
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07863291B2
反応ノート
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