Ammonium formate → 9-(1-Acetyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-6-yl)-3-(2-methyl-pyrimidin-5-yl)-nonanoic acid ethyl ester
反応式
[CH2:1]([O:3][C:4](=[O:32])[CH2:5][CH:6]([C:25]1[CH:26]=[N:27][C:28]([CH3:31])=[N:29][CH:30]=1)[CH:7]=[CH:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]1[N:18]=[C:17]2[N:19]([C:22](=[O:24])[CH3:23])[CH2:20][CH2:21][C:16]2=[CH:15][CH:14]=1)[CH3:2].C([O-])=O.[NH4+]>CCO.[Pd]>[CH2:1]([O:3][C:4](=[O:32])[CH2:5][CH:6]([C:25]1[CH:26]=[N:27][C:28]([CH3:31])=[N:29][CH:30]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]1[N:18]=[C:17]2[N:19]([C:22](=[O:24])[CH3:23])[CH2:20][CH2:21][C:16]2=[CH:15][CH:14]=1)[CH3:2]参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 23-10 (0.150 g, 0.34 mmol), ammonium formate (0.192 g, 3.09 mmol), and 10% Pd/C (0.150 g) in EtOH (25 rnL) was refluxed for 15 minutes. Filtration through celite and evaporative removal of the solvent followed by purification by PCTLC (0–10% MeOH-CHCl3) afforded 0.050 g of 23-11.
後処理
- filtrationFiltration through celite
- customremoval of the solvent
- customfollowed by purification by PCTLC (0–10% MeOH-CHCl3)
出典と根拠
- ORDレコード
- ord-ac1a33a739b2463388f1beefdab9ded5
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07153862B2
反応ノート
読み込み中…