反応式
[NH2:1][C:2]1[S:6][C:5]2[CH2:7][CH2:8][CH2:9][CH2:10][C:4]=2[C:3]=1[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12].N1C=CC=CC=1.[Cl:24][C:25]1[CH:26]=[C:27]([S:32](Cl)(=[O:34])=[O:33])[CH:28]=[CH:29][C:30]=1[Cl:31].O>C(Cl)Cl>[Cl:24][C:25]1[CH:26]=[C:27]([S:32]([NH:1][C:2]2[S:6][C:5]3[CH2:7][CH2:8][CH2:9][CH2:10][C:4]=3[C:3]=2[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])(=[O:33])=[O:34])[CH:28]=[CH:29][C:30]=1[Cl:31]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
tert-Butyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate (12.26 g, 48.4 mmol) was dissolved in DCM (150 ml), and pyridine (6.0 ml, 74 mmol) was added thereto. A solution of 3,4-dichlorobenzenesulfonyl chloride (8.4 ml, 54 mmol) was then added, and the mixture was heated for 17 h under reflux and then cooled to room temperature. Water was added (100 ml), and stirring was carried out overnight at room temperature. The phases were then separated (pH organic phase≈2), washed with saturated NaHCO3 solution, dried (sodium sulfate) and concentrated in vacuo.
後処理
- temperaturethe mixture was heated for 17 h
- temperatureunder reflux
- customThe phases were then separated (pH organic phase≈2),
- washwashed with saturated NaHCO3 solution
- dry with materialdried (sodium sulfate)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-9b9e7296bb0049d68a884740daff09a0
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08119633B2
関連ノート
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