Ammonium Chloride → HCID 58734277、化合物
反応式
C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[Cl:11][C:12]1[C:13]([CH:19]([S:28]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][N:32]=2)(=[O:30])=[O:29])[C:20]2[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:21]=2[F:27])=[CH:14][C:15]([NH2:18])=[N:16][CH:17]=1.[CH3:38][S:39](Cl)(=[O:41])=[O:40].[Cl-].[NH4+]>ClCCl.O1CCCC1>[Cl:11][C:12]1[C:13]([CH:19]([S:28]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][N:32]=2)(=[O:29])=[O:30])[C:20]2[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:21]=2[F:27])=[CH:14][C:15]([NH:18][S:39]([CH3:38])(=[O:41])=[O:40])=[N:16][CH:17]=1参加物
実験手順
Under an argon atmosphere, a tetrahydrofuran solution (1M, 0.705 ml, 0.71 mmol) of sodium bis(trimethylsilyl)amide was added to a tetrahydrofuran (4 ml) solution of [5-chloro-4-[(5-chloropyridin-2-ylsulfonyl)(2,5-difluorophenyl)methyl]pyridin-2-yl]amine (92 mg, 0.21 mmol) at 0° C. The resulting mixture was stirred for 30 minutes. To the reaction mixture was added methanesulfonyl chloride (0.055 ml, 0.71 mmol). At the same temperature, the resulting mixture was stirred for 2 hours. The temperature of the reaction mixture was then raised to room temperature. To the reaction mixture was added a saturated aqueous solution of ammonium chloride. The product thus obtained was extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue thus obtained was subjected to flash silica gel column chromatography. The fraction obtained from the dichloromethane:ethyl acetate=19:1 eluate was concentrated under reduced pressure. The residue thus obtained was washed with an ethanol/hexane mixed solvent and then, collected by filtration to give the title compound (27 mg, 0.053 mmol, 25%) as a white solid.
後処理
- stirringAt the same temperature, the resulting mixture was stirred for 2 hours
- customThe product thus obtained
- extractionwas extracted with diethyl ether
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure
- customThe residue thus obtained
- concentrationethyl acetate=19:1 eluate was concentrated under reduced pressure
- customThe residue thus obtained
- washwas washed with an ethanol/hexane mixed solvent
- filtrationcollected by filtration
出典と根拠
- ORDレコード
- ord-53572354657544aba6fbef20db6d74e3
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07932271B2
反応ノート
読み込み中…