反応式
[CH3:1][O:2][C:3]([C:5]1[C:13]2[C:8](=[N:9][CH:10]=[C:11]([F:14])[CH:12]=2)[N:7]([S:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)(=[O:17])=[O:16])[C:6]=1[CH3:24])=[O:4].[Br:25]N1C(C)(C)C(=O)N(Br)C1=O>ClCCCl>[CH3:1][O:2][C:3]([C:5]1[C:13]2[C:8](=[N:9][CH:10]=[C:11]([F:14])[CH:12]=2)[N:7]([S:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)(=[O:17])=[O:16])[C:6]=1[CH2:24][Br:25])=[O:4]参加物
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of 1-benzenesulfonyl-5-fluoro-2-methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester (13.9 g, 39.9 mmol), 1,3-dibromo-5,5-dimethylhydantoin (12.6 g, 39.9 mmol) and 1,1-azobis(cyclohexanecarbonitrile) (1.95 g, 8.0 mmol) in 1,2-dichloroethane (150 mL) was heated under reflux for 90 minutes then stirred at ambient temperature for 16 hours. The reaction mixture was washed with saturated aqueous sodium thiosulfate solution. The organic layer was dried (Na2SO4) then filtered. The filtrate was stirred with flash silica gel, filtered and the filtrate evaporated under reduced pressure. The resultant residue was triturated with diethyl ether/pentane (1:1) to afford the title compound as a cream solid (15.9 g, 93%). 1H NMR (400 MHz, CDCl3): 8.47-8.44 (m, 2H), 8.32 (dd, J=2.8, 1.1 Hz, 1H), 8.04 (dd, J=8.5, 2.8 Hz, 1H), 7.64-7.64 (m, 1H), 7.54-7.53 (m, 2H), 5.68 (s, 2H), 4.00 (s, 3H).
後処理
- temperaturewas heated
- temperatureunder reflux for 90 minutes
- washThe reaction mixture was washed with saturated aqueous sodium thiosulfate solution
- dry with materialThe organic layer was dried (Na2SO4)
- filtrationthen filtered
- stirringThe filtrate was stirred with flash silica gel
- filtrationfiltered
- customthe filtrate evaporated under reduced pressure
- customThe resultant residue was triturated with diethyl ether/pentane (1:1)
出典と根拠
- ORDレコード
- ord-50494b488cbe4e83a33254f9337a10b1
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09440976B2
関連ノート
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