(3R)-1-Methyl-3-PyrrolidinaMine hydrochloride → 4-amino-5-ethoxy-2-fluoro-N-[(3R)-1-methylpyrrolidin-3-yl]benzamide
反応式
[NH2:1][C:2]1[C:17]([O:18][CH2:19][CH3:20])=[CH:16][C:5]([C:6]([NH:8][CH:9]2[CH2:14][CH2:13][N:12]([CH3:15])[CH2:11]C2)=[O:7])=[C:4]([F:21])[CH:3]=1.Cl.Cl.CN1CC[C@@H](N)C1>>[NH2:1][C:2]1[C:17]([O:18][CH2:19][CH3:20])=[CH:16][C:5]([C:6]([NH:8][C@@H:9]2[CH2:14][CH2:13][N:12]([CH3:15])[CH2:11]2)=[O:7])=[C:4]([F:21])[CH:3]=1参加物
3
実験手順
The title compound was prepared by an analogous method to the preparation of Intermediate 169, on a 0.5 mmol scale, utilising (3R)-1-methylpyrrolidin-3-amine dihydrochloride (Intermediate 184; 129 mg, 0.75 mmol), as a white solid (95 mg, 68%).
出典と根拠
- ORDレコード
- ord-4786d7962eaa4743991a7ef4cd931654
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07709471B2
反応ノート
読み込み中…