Ammonia → (2-(2-Methylpyrimidin-5-yl)tetrahydrofuran-2-yl)methanamine
反応式
[CH3:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2([C:13]#[N:14])[CH2:12][CH2:11][CH2:10][O:9]2)=[CH:4][N:3]=1.N>CO.[Ni]>[CH3:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2([CH2:13][NH2:14])[CH2:12][CH2:11][CH2:10][O:9]2)=[CH:4][N:3]=1参加物
5
実験手順
2-(2-Methylpyrimidin-5-yl)tetrahydrofuran-2-carbonitrile (18 mg, 0.095 mmol) was dissolved in MeOH(5 ml) and 7M NH3 in MeOH (1 ml). Argon was bubbled through the solution. Raney Nickel (6 mg, 0.1 mmol) was added and the flask was fitted with a H2-balloon and stirred at room temperature for 1½ hour. Reaction was filtred through a plug of celite and concentrated in vacuo. Used for next step without further purification. LC-MS (m/z) 194.0 (MH+), tR (minutes, Method D)=0.17.
後処理
- customArgon was bubbled through the solution
- customthe flask was fitted with a H2-balloon
- customReaction
- concentrationconcentrated in vacuo
- customUsed for next step without further purification
出典と根拠
- ORDレコード
- ord-6221c7e565f74f5e8f6930fb652ed982
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09102591B2
反応ノート
読み込み中…