HCID 69003268、化合物 → N-[4-(3-Amino-4-methylamino-phenoxy)-pyridin-2-yl]-2-(2-hydroxymethyl-pyrrolidin-1-yl)-acetamide
反応式
[OH:1][CH2:2][CH:3]1[CH2:7][CH2:6][CH2:5][N:4]1[CH2:8][C:9]([NH:11][C:12]1[CH:17]=[C:16]([O:18][C:19]2[CH:24]=[CH:23][C:22]([NH:25][CH3:26])=[C:21]([N+:27]([O-])=O)[CH:20]=2)[CH:15]=[CH:14][N:13]=1)=[O:10]>CO.[Pd]>[NH2:27][C:21]1[CH:20]=[C:19]([CH:24]=[CH:23][C:22]=1[NH:25][CH3:26])[O:18][C:16]1[CH:15]=[CH:14][N:13]=[C:12]([NH:11][C:9](=[O:10])[CH2:8][N:4]2[CH2:5][CH2:6][CH2:7][CH:3]2[CH2:2][OH:1])[CH:17]=1参加物
4
実験手順
2-(2-Hydroxymethyl-pyrrolidin-1-yl)-N-[4-(4-methylamino-3-nitro-phenoxy)-pyridin-2-yl]-acetamide was hydrogenated in methanol in the presence of Pd C for 4 hours. The catalyst was removed via filtration through Celite and filtrate was concentrated to give N-[4-(3-Amino-4-methylamino-phenoxy)-pyridin-2-yl]-2-(2-hydroxymethyl-pyrrolidin-1-yl)-acetamide. MS: MH+=372.4.
後処理
- customThe catalyst was removed via filtration through Celite and filtrate
- concentrationwas concentrated
出典と根拠
- ORDレコード
- ord-b17dfceed05a4588918be690fe79d9fc
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08415382B2
反応ノート
読み込み中…