Sodium Hydroxide → 2-{1-[4-(dipropylamino)butyl]-4-piperidinyl}-N,N-bis(1H-imidazol-2-ylmethyl)acetamide
反応式
Cl.Cl.Cl.[NH:4]1[CH:8]=[CH:7][N:6]=[C:5]1[CH2:9][N:10]([CH2:20][C:21]1[NH:22][CH:23]=[CH:24][N:25]=1)[C:11](=[O:19])[CH2:12][CH:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1.[CH2:26]([N:29]([CH2:35][CH2:36][CH3:37])[CH2:30][CH2:31][CH2:32][CH:33]=O)[CH2:27][CH3:28].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>C(O)(=O)C>[CH2:35]([N:29]([CH2:26][CH2:27][CH3:28])[CH2:30][CH2:31][CH2:32][CH2:33][N:16]1[CH2:17][CH2:18][CH:13]([CH2:12][C:11]([N:10]([CH2:20][C:21]2[NH:22][CH:23]=[CH:24][N:25]=2)[CH2:9][C:5]2[NH:4][CH:8]=[CH:7][N:6]=2)=[O:19])[CH2:14][CH2:15]1)[CH2:36][CH3:37]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
The compound 45 and 4-(dipropylamino)butanal (55.6 mg) were added and a 10% acetic acid-anhydrous dimethyl formamide solution (3 mL) was stirred under an argon atmosphere for 5 minutes. To the reaction solution, sodium triacetoxyborohydride (103 mg) was added, followed by stirring at room temperature for 15 hours. To the reaction solution, an aqueous 2N sodium hydroxide solution (10 mL) was added and the aqueous layer was extracted three times with ethyl acetate. The organic layer was collected, washed with saturated brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography to obtain the title compound (86.4 mg) having the following physical properties.
後処理
- extractionthe aqueous layer was extracted three times with ethyl acetate
- customThe organic layer was collected
- washwashed with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- distillationthe solvent was distilled off
- customThe residue was purified by silica gel column chromatography
出典と根拠
- ORDレコード
- ord-2f2489421e5740369ee5e11b4fb07974
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822459B2
反応ノート
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