反応式
[CH2:1]([SH:6])[CH2:2][CH2:3][CH2:4][CH3:5].[H-].[Na+].Cl[C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([C:16]#[N:17])[N:11]=1>O1CCCC1>[C:16]([C:12]1[CH:13]=[CH:14][CH:15]=[C:10]([S:6][CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[N:11]=1)#[N:17]参加物
5
実験手順
Pentyl mercaptan (0.83 g, 7.9 mmol) was dissolved in tetrahydrofuran (100 ml) and added dropwise to sodium hydride (60% oil, 0.35 g, 8.7 mmol). The reaction mixture was stirred at room temperature for 1 hr. A solution of 2-chloro-6-cyanopyridine (1.00 g, 7.2 mmol) in tetrahydrofuran (10 ml) was added to the mixture, and the mixture was stirred at room temperature for 18 hrs. The reaction mixture was concentrated under reduced pressure, diluted with water and extracted with ethyl acetate. The extract was washed with saturated brine and dried. The solvent was evaporated under reduced pressure to give the titled compound (1.48 g, ca. 100%) as an oil.
後処理
- stirringthe mixture was stirred at room temperature for 18 hrs
- concentrationThe reaction mixture was concentrated under reduced pressure
- additiondiluted with water
- extractionextracted with ethyl acetate
- washThe extract was washed with saturated brine
- customdried
- customThe solvent was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-499329ddf1794e0f8a13f03ba9b2dce8
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07767665B2
関連ノート
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