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Triethylamine → 5-Chloro-N-[2-(dimethylamino)ethyl]-2-thiophenesulfonamide

HRID 558521
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HRID 558521 반응식
[CH3:1][N:2]([CH3:6])[CH2:3][CH2:4][NH2:5].[Cl:7][C:8]1[S:12][C:11]([S:13](Cl)(=[O:15])=[O:14])=[CH:10][CH:9]=1.C(N(CC)CC)C>C1COCC1>[CH3:1][N:2]([CH3:6])[CH2:3][CH2:4][NH:5][S:13]([C:11]1[S:12][C:8]([Cl:7])=[CH:9][CH:10]=1)(=[O:15])=[O:14]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 66053N,N-DimethylethylenediamineHCID 27339255-Chlorothiophene-2-sulfonyl chloride

생성물 1

HCID 50132195-Chloro-N-[2-(dimethylamino)ethyl]-2-thiophenesulfonamide수율 99.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 2-dimethylamino-ethylamine (1.61 g, 13.8 mmol) in THF (20 mL) was added at 0° C. (ice water bath) commercially available 5-chloro-thiophene-2-sulfonyl chloride (1.0 g, 4.61 mmol) and triethylamine (0.71 mL, 5.07 mmol). The reaction mixture was stirred at room temperature for 16 h and evaporated. The crude product was further purified by flash chromatography (ethyl acetate/MeOH) to yield the title compound (1.23 g, 99%) as a light yellow oil. MS (ISP) 269.0 [(M+H)+].

후처리

  1. customevaporated
  2. customThe crude product was further purified by flash chromatography (ethyl acetate/MeOH)

출처 및 근거

ORD 기록
ord-7f7fc52525af442f8531155e09defdea
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063048B2

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