Dichloromethane → (S)-2-(5-(1-methylpyrrolidin-2-yl)pyridin-3-yloxy)ethanamine
反応式
[CH3:1][N:2]1[CH2:6][CH2:5][CH2:4][C@H:3]1[C:7]1[CH:8]=[C:9]([O:13][CH2:14][CH2:15][NH:16]C(=O)OC(C)(C)C)[CH:10]=[N:11][CH:12]=1.C(Cl)Cl>FC(F)(F)C(O)=O>[CH3:1][N:2]1[CH2:6][CH2:5][CH2:4][C@H:3]1[C:7]1[CH:8]=[C:9]([O:13][CH2:14][CH2:15][NH2:16])[CH:10]=[N:11][CH:12]=1参加物
4
実験手順
Preparation 12a: (S)-tert-butyl 2-(5-(1-Methylpyrrolidin-2-yl)pyridin-3-yloxy)ethylcarbamate (preparation 11) (105 mg, 0.33 mmol) was stirred in trifluoroacetic acid (1 mL) and DCM (5 mL) for 1.5 h. The reaction mixture was evaporated, then co-evaporated with DCM (×5) and 20% ammonia in MeOH. The crude product was purified by flash chromatography (5% [20% ammonia in MeOH] in DCM) to give the title compound as a yellow oil (62 mg, 85%).
後処理
- customThe reaction mixture was evaporated
- customThe crude product was purified by flash chromatography (5% [20% ammonia in MeOH] in DCM)
出典と根拠
- ORDレコード
- ord-4a9d04f5ab4c4feea4fd7650066e6039
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08980276B2
反応ノート
読み込み中…