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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 88539500, 화합물 → HCID 16102886, 화합물

HRID 1404565
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인쇄 미리보기

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HRID 1404565 반응식
[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
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참가 물질

4

반응물 2

HCID 88539500HCID 88539500, 화합물HCID 178418332HCID 178418332, 화합물2회

생성물 1

HCID 16102886HCID 16102886, 화합물수율 82.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-48 °C

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-024abc198e904f38b00e0c9ba9dd0ec0
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08912221B2

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