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5-Chloro-2,4-difluorobenzenesulphonyl chloride → 5-chloro-N-(2,4-dimethoxybenzyl)-2,4-difluoro-N-(pyrimidin-2-yl)benzenesulfonamide

HRID 509120
ノート
印刷プレビュー

反応式

HRID 509120 の反応式
[CH3:1][O:2][C:3]1[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:4]=1[CH2:5][NH:6][C:7]1[N:12]=[CH:11][CH:10]=[CH:9][N:8]=1.C[Si](C)(C)N[Si](C)(C)C.[Li].[Cl:29][C:30]1[CH:31]=[C:32]([S:38](Cl)(=[O:40])=[O:39])[C:33]([F:37])=[CH:34][C:35]=1[F:36]>O1CCCC1>[Cl:29][C:30]1[C:35]([F:36])=[CH:34][C:33]([F:37])=[C:32]([S:38]([N:6]([CH2:5][C:4]2[CH:13]=[CH:14][C:15]([O:17][CH3:18])=[CH:16][C:3]=2[O:2][CH3:1])[C:7]2[N:8]=[CH:9][CH:10]=[CH:11][N:12]=2)(=[O:40])=[O:39])[CH:31]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 27735275-Chloro-2,4-difluorobenzenesulphonyl chlorideHCID 55026262N-[(2,4-dimethoxyphenyl)methyl]pyrimidin-2-amineHCID 57426343Lithium bis(trimethylsilyl)amide

生成物 1

HCID 580422645-chloro-N-(2,4-dimethoxybenzyl)-2,4-difluoro-N-(pyrimidin-2-yl)benzenesulfonamide収率 19%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒
2 回

反応条件

温度
0 °C

実験手順

A solution of (2,4-dimethoxybenzyl)-pyrimidin-2-yl-amine (Preparation 38, 736 mg, 3 mmol) in anhydrous tetrahydrofuran (20 mL) was cooled to −78° C. before the addition of lithium(hexamethyldisilazane) (1M solution in tetrahydrofuran, 3.30 mL, 3.30 mmol). The reaction was allowed to warm to 0° C. for 30 minutes before cooling again to −78° C. The resulting solution was added to a solution of 3-chloro-4,6-difluorobenzenesulfonyl chloride (890 mg, 3.6 mmol) in tetrahydrofuran (10 mL) at −78° C. After 30 minutes at this temperature the reaction was warmed to room temperature and stirred for 24 hours. The reaction was quenched by the addition of saturated aqueous ammonium chloride solution and extracted into ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified using silica gel column chromatography (50-100% dichloromethane in heptane gradient elution) to afford the title compound as a white solid (260 mg, 19%).

後処理

  1. temperaturebefore cooling again to −78° C
  2. temperatureAfter 30 minutes at this temperature the reaction was warmed to room temperature
  3. customThe reaction was quenched by the addition of saturated aqueous ammonium chloride solution
  4. extractionextracted into ethyl acetate
  5. washThe organic layer was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified
  9. washsilica gel column chromatography (50-100% dichloromethane in heptane gradient elution)

出典と根拠

ORDレコード
ord-8bc57f50556741e795a7db7e50eb3ea3
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09096558B2

反応ノート

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