Sodium Bicarbonate → N-(4-dipropylaminomethylphenyl)-4-{[(1H-imidazol-2-ylmethyl)-(5-methylpyrazine-2-ylmethyl)-amino]-methyl}-benzamide
反応式
C(N(CCC)[C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:27])[C:13]2[CH:18]=[CH:17][C:16]([CH2:19][NH:20][CH2:21][C:22]3[NH:23][CH:24]=[CH:25][N:26]=3)=[CH:15][CH:14]=2)=[CH:7][CH:6]=1)CC.[CH3:31][C:32]1[N:33]=[CH:34][C:35]([CH:38]=O)=[N:36][CH:37]=1.[C:40]([BH3-])#[N:41].[Na+].C(=O)(O)[O-].[Na+]>CO.C(O)(=O)C>[CH2:6]([N:41]([CH2:40][C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12](=[O:27])[C:13]2[CH:14]=[CH:15][C:16]([CH2:19][N:20]([CH2:21][C:22]3[NH:26][CH:25]=[CH:24][N:23]=3)[CH2:38][C:35]3[CH:34]=[N:33][C:32]([CH3:31])=[CH:37][N:36]=3)=[CH:17][CH:18]=2)=[CH:9][CH:10]=1)[CH2:7][CH2:8][CH3:9])[CH2:5][CH3:10]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
The compound (82.2 mg) obtained in Example 47-3 was dissolved in methanol (5.0 ml) and added with the compound (35.9 mg) obtained in Example 73-1, followed by the addition of sodium cyanoborohydride (36.9 mg). Then, the reaction solution was adjusted to about pH 5 with acetic acid, followed by stirring at room temperature for 16 hours. The reaction solution was added with a saturated aqueous sodium bicarbonate solution and then extracted with chloroform. The organic layer was washed with saturated saline solution and then dried with anhydrous sodium sulfate. Subsequently, the solvent was distilled off. The resulting crude product was purified through silica gel column chromatography (chloroform/methanol) and treated with hydrochloric acid, thereby obtaining hydrochloride (84.0 mg) of the subject compound as a pale-yellow solid.
後処理
- extractionextracted with chloroform
- washThe organic layer was washed with saturated saline solution
- dry with materialdried with anhydrous sodium sulfate
- distillationSubsequently, the solvent was distilled off
- customThe resulting crude product was purified through silica gel column chromatography (chloroform/methanol)
- additiontreated with hydrochloric acid
出典と根拠
- ORDレコード
- ord-44f99cb136fb471086d9e792bf8b32e8
- 出典データセット
- uspto-grants-2010_11
- 特許番号
- US07833991B2
反応ノート
読み込み中…