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N,N'-Dimethylethylenediamine → HCID 67609006, 화합물

HRID 1467976
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HRID 1467976 반응식
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2([F:13])[F:12].[CH3:14][S:15]([O-:17])=[O:16].[Na+].CNCCNC>CS(C)=O>[F:12][C:5]1([F:13])[C:4]2[C:8](=[CH:9][CH:10]=[C:2]([S:15]([CH3:14])(=[O:17])=[O:16])[CH:3]=2)[NH:7][C:6]1=[O:11]
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참가 물질

5

반응물 3

HCID 8070N,N'-DimethylethylenediamineHCID 2733271Sodium methanesulfinateHCID 226077815-bromo-3,3-difluoro-2,3-dihydro-1H-indol-2-one

생성물 1

HCID 67609006HCID 67609006, 화합물수율 58.7%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
120 °C

실험 절차

To a stirred solution of 5-bromo-3,3-difluoroindolin-2-one (5.0 g, 20 mmol) in DMSO (50 mL), sodium methanesulfinate (3.0 g, 30 mmol), copper(I) trifluoromethane-sulfonate benzene complex (1.52 g, 3.022 mmol) and N,N′-dimethylethylenediamine (0.33 mL, 3.022 mmol) were added and stirred at 120° C. for 14 h. The reaction was quenched with water and the mixture was extracted with ethyl acetate. The organic layer was concentrated in vacuo and resulting residue was purified by flash column chromatography to give the title product (2.9 g, 58.2%); MS: 247.9 (M+1).

후처리

  1. customThe reaction was quenched with water
  2. extractionthe mixture was extracted with ethyl acetate
  3. concentrationThe organic layer was concentrated in vacuo
  4. customresulting residue
  5. customwas purified by flash column chromatography

출처 및 근거

ORD 기록
ord-4dfb267ff81c4319a9c35b4b3add4a02
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09000175B2

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