Methanol → 4-Cyclopropylpyridin-3-amine
反応式
[Cl-].[NH4+].[CH:3]1([C:6]2[CH:11]=[CH:10][N:9]=[CH:8][C:7]=2[N+:12]([O-])=O)[CH2:5][CH2:4]1.CO>C1COCC1.C(Cl)(Cl)Cl.[Zn]>[CH:3]1([C:6]2[CH:11]=[CH:10][N:9]=[CH:8][C:7]=2[NH2:12])[CH2:5][CH2:4]1参加物
7
実験手順
Zinc powder (223.2 mg, 3.41 mmol) and ammonium chloride solution (365 mg, 6.8 mmol) were added to a stirred solution of 4-cyclopropyl-3-nitropyridine (70 mg, 0.426 mmol) in dry THF (2 mL) at 0° C. and the resulting mixture was stirred at room temperature for 1 hour. The reaction was monitored by TLC (10% methanol in CHCl3). The organic layer was concentrated and washed with pentane to afford 450 mg of the product (100% yield).
後処理
- concentrationThe organic layer was concentrated
- washwashed with pentane
出典と根拠
- ORDレコード
- ord-05a9a7d74b5040ec97a2758b1b7038b9
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08946260B2
反応ノート
読み込み中…