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HCID 88539500、化合物 → HCID 16102886、化合物

HRID 1404565
ノート
印刷プレビュー

反応式

HRID 1404565 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5](/[CH:8]=[N:9]/[S@:10]([C:12]([CH3:15])([CH3:14])[CH3:13])=[O:11])=[C:4]([F:16])[CH:3]=1.[CH3:17][Mg]Cl>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH:9][S@:10]([C:12]([CH3:13])([CH3:15])[CH3:14])=[O:11])[CH3:17])=[C:4]([F:16])[CH:3]=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

4

反応物 2

HCID 88539500HCID 88539500、化合物HCID 178418332HCID 178418332、化合物2 回

生成物 1

HCID 16102886HCID 16102886、化合物収率 82.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-48 °C

実験手順

To a solution of (S)-2-methyl-propane-2-sulfinic acid 1-(4-bromo-2-fluoro-phenyl)-meth-(E)-ylideneamide (4.5 g, 14.7 mmol) in DCM (80 ml) was added methylmagnesium chloride (7.35 ml, 22.0 mmol, 3M solution in ether) dropwise at −48° C. After 1 h additional methylmagnesium chloride (2.45 ml, 7.35 mmol, 3M solution in ether) was added dropwise and the reaction mixture was stirred at −48° C. for 6 h. The reaction was then quenched by addition of sat. NH4Cl solution and the mixture was extracted three times with DCM. The combined organic layers were dried with Na2SO4 and evaporated. The remaining white solid was purified by chromatography (silica gel; heptane/EtOAc 2:1-1:1) to obtain the title compound as white solid (3.89 g, 82%).

後処理

  1. customThe reaction was then quenched by addition of sat. NH4Cl solution
  2. extractionthe mixture was extracted three times with DCM
  3. dry with materialThe combined organic layers were dried with Na2SO4
  4. customevaporated
  5. customThe remaining white solid was purified by chromatography (silica gel; heptane/EtOAc 2:1-1:1)

出典と根拠

ORDレコード
ord-024abc198e904f38b00e0c9ba9dd0ec0
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912221B2

反応ノート

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