1-(8-Amino-quinolin-7-yl)-propan-1-ol → 1-(8-Amino-quinolin-7-yl)-propan-1-one
反応式
[NH2:1][C:2]1[C:3]([CH:12]([OH:15])[CH2:13][CH3:14])=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2>O=[Mn]=O.C(Cl)Cl>[NH2:1][C:2]1[C:3]([C:12](=[O:15])[CH2:13][CH3:14])=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2参加物
4
実験手順
In a similar fashion using route 27 general procedure 68, 1-(8-amino-quinolin-7-yl)-propan-1-ol 408 (1.0 g, 4.95 mmol), MnO2 powder (4.3 g, 49.5 mmol) and DCM (10 ml) gave the title compound (800 mg, 80%) which was used in the next step without further purification.
出典と根拠
- ORDレコード
- ord-eb960c037c2942f39a8178ea2e689ace
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09102688B2
反応ノート
読み込み中…