反応式
I[C:2]1[CH:7]=[N:6][CH:5]=[C:4]([I:8])[N:3]=1.[Na].[CH2:10]([OH:12])[CH3:11]>>[I:8][C:4]1[CH:5]=[N:6][CH:7]=[C:2]([O:12][CH2:10][CH3:11])[N:3]=1参加物
4
実験手順
2,6-Diiodopyrazine (12 g, 36.14 mmol) was added to a solution of sodium (0.83 g, 36.10 mmol) in ethanol (75 ml). The solution was refluxed for 1 h, the solvent removed under vacuum, water (40 ml) added and extracted into dichloromethane (4×200 ml). The solvent was removed under vacuum and the residue chromatographed through silica-gel using dichloromethane as eluant to give 2-iodo-6-ethoxy pyrazine (6.5 g). m.p. 36°-37° C.; δ (60 MHz, CDCl3) 1.30 (3H, t, J=7 Hz, Me); 4.35 (2H, q, J=7 Hz, CH2Me); 8.07 (1H, s, pyrazine-H): 8.35 (1H, s, pyrazine-H).
後処理
- temperatureThe solution was refluxed for 1 h
- customthe solvent removed under vacuum, water (40 ml)
- additionadded
- extractionextracted into dichloromethane (4×200 ml)
- customThe solvent was removed under vacuum
- customthe residue chromatographed through silica-gel
出典と根拠
- ORDレコード
- ord-9fb4e3fea5744389be333f882c290680
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05260293
関連ノート
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