Methyl 2-(Methylthio)pyrimidine-5-carboxylate → (2-(Methylsulfanyl)pyrimidin-5-yl)methanol
反応式
[CH3:1][S:2][C:3]1[N:8]=[CH:7][C:6]([C:9](OC)=[O:10])=[CH:5][N:4]=1.[H-].C([Al+]CC(C)C)C(C)C>C1COCC1>[CH3:1][S:2][C:3]1[N:8]=[CH:7][C:6]([CH2:9][OH:10])=[CH:5][N:4]=1参加物
4
反応条件
- 温度
- -78 °C
実験手順
To a solution of methyl 2-(methylsulfanyl)pyrimidine-5-carboxylate (N1) (023 g, 1.2 mmol) in 20 mL THF at −78° C. was added diisobutylaluminum hydride (3.2 mL, 1.0 M solution in toluene). The reaction mixture stirred for 40 min at −78° C., and then additional diisobutylaluminum hydride (5 eq.) was added dropwise. The reaction mixture was stirred for 2 h, and then quenched with concentrated acetic acid. The reaction mixture was warmed to room temperature and filtered to obtain a biphasic solution. The layers were separated, and the organics were dried over sodium sulfate, filtered, and concentrated to afford [2-(methylsulfanyl)pyrimidin-5-yl]methanol (N2) that gave a mass ion (ES+) of 157.1 for M+H+.
後処理
- stirringThe reaction mixture was stirred for 2 h
- customquenched with concentrated acetic acid
- temperatureThe reaction mixture was warmed to room temperature
- filtrationfiltered
- customto obtain a biphasic solution
- customThe layers were separated
- dry with materialthe organics were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-6bc0b31bddfd465fa02ef70a55890429
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09199939B2
反応ノート
読み込み中…