Hydrochloric Acid → 5-Aminomethyl-2-(2-pyrrolidin-1-yl-ethoxy)-phenol
反応式
CO[N:3]=[CH:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][N:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([OH:19])[CH:6]=1.Cl>C(O)C.[Pd]>[NH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][N:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([OH:19])[CH:6]=1参加物
5
実験手順
An amount of 3-Hydroxy-4-(2-pyrrolidin-1-yl-ethoxy)-benzaldehyde O-methyl-oxime (50 mg, 0.18 mmol) is dissolved in ethanol (10 mL). Then hydrogen chloride (0.130 mL) is added, followed by 10% Pd/C (5.0 mg). After hydrogenation at 35 psi for 3 h, the solution is filtered through Celite and evaporated to dryness. The residue is recrystallized from ethyl acetate to give 45 mg of crude product as a white solid. MS (ESI) m/z 283.1 (M+1)
後処理
- filtrationthe solution is filtered through Celite
- customevaporated to dryness
- customThe residue is recrystallized from ethyl acetate
出典と根拠
- ORDレコード
- ord-70fc5c51403d4a6980e4cbed23949ed9
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07713994B2
反応ノート
読み込み中…