反応式
[C:1](Cl)(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].ClCCl.[CH3:22][C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][C:28]=1[C:29]([NH:31][C:32]1[CH:33]=[CH:34][C:35]([C:39]([N:41]2[C:47]3[CH:48]=[CH:49][C:50]([Cl:52])=[CH:51][C:46]=3[CH:45]([OH:53])[CH2:44][CH2:43][CH2:42]2)=[O:40])=[C:36]([CH3:38])[CH:37]=1)=[O:30].N1C=CC=CC=1>O>[Cl:52][C:50]1[CH:49]=[CH:48][C:47]2[N:41]([C:39](=[O:40])[C:35]3[CH:34]=[CH:33][C:32]([NH:31][C:29](=[O:30])[C:28]4[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=4[CH3:22])=[CH:37][C:36]=3[CH3:38])[CH2:42][CH2:43][CH2:44][CH:45]([O:53][C:1](=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[C:46]=2[CH:51]=1参加物
6
実験手順
Palmitoyl chloride (1.24 ml, 4.4 mmol) was added to a dichloromethane (20 ml) solution of tolvaptan (2.00 g, 4.4 mmol) and pyridine (0.40 ml, 5.0 mmol), and the mixture was stirred at room temperature over night. Water was added to the reaction mixture and the mixture was extracted with dichloromethane. The combined organic layer was washed with water and an aqueous saturated sodium chloride solution, and dried over magnesium sulfate. After filtration and concentration, the residue was purified by silica gel chromatography (n-hexane:ethyl acetate) to thereby obtain 2.25 g (74%) of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}hexadecanoate as amorphous.
後処理
- extractionthe mixture was extracted with dichloromethane
- washThe combined organic layer was washed with water
- dry with materialan aqueous saturated sodium chloride solution, and dried over magnesium sulfate
- filtrationAfter filtration and concentration
- customthe residue was purified by silica gel chromatography (n-hexane:ethyl acetate)
出典と根拠
- ORDレコード
- ord-9567796359444165a637330ea1574e1c
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08669229B2
関連ノート
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