3-Methoxypropanoyl chloride → 5-(4-ethylphenyl)-1-(3-methoxypropanoyl)-N-phenylpiperidine-3-carboxamide
反応式
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[CH2:14][NH:13][CH2:12][CH:11]([C:15]([NH:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[O:16])[CH2:10]2)=[CH:5][CH:4]=1)[CH3:2].[CH3:24][O:25][CH2:26][CH2:27][C:28](Cl)=[O:29]>>[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[CH2:14][N:13]([C:28](=[O:29])[CH2:27][CH2:26][O:25][CH3:24])[CH2:12][CH:11]([C:15]([NH:17][C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)=[O:16])[CH2:10]2)=[CH:7][CH:8]=1)[CH3:2]参加物
3
実験手順
62 mg (0.18 mmol) of 5-(4-ethylphenyl)-N-phenylpiperidine-3-carboxamide (Example 17A) and 33 mg (0.27 mmol, 1.5 eq.) of methoxypropionyl chloride were reacted according to General Method 2. Yield: 65 mg (91% of theory)
出典と根拠
- ORDレコード
- ord-65a47e3107dd445ab8d4b987a9a12574
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987248B2
反応ノート
読み込み中…