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Ethanesulfonyl chloride → N-(4-bromo-2-fluorobenzyl)ethanesulfonamide

HRID 1842986
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HRID 1842986 반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH2:7])=[C:4]([F:10])[CH:3]=1.[CH2:11]([S:13](Cl)(=[O:15])=[O:14])[CH3:12]>N1C=CC=CC=1>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH:7][S:13]([CH2:11][CH3:12])(=[O:15])=[O:14])=[C:4]([F:10])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11667Ethanesulfonyl chlorideHCID 3770848(4-Bromo-2-fluorophenyl)methanamine

생성물 1

HCID 70816043N-(4-bromo-2-fluorobenzyl)ethanesulfonamide

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
0 °C

실험 절차

4-Bromo-2-fluorobenzylamine (924 mg, 4.53 mmol) was dissolved in pyridine and ethane sulfonyl chloride (0.82 mL, 8.60 mmol) was added to the solution at 0° C. The mixture was stirred for 1 h at 0° C. Then, the mixture was quenched with 1N HCl and extracted with ethyl acetate (EtOAc). Drying (MgSO4) and evaporation of the ethyl acetate followed and the residue was purified by CC (eluent EtOAc/n-hexane) to yield N-(4-bromo-2-fluorobenzyl)ethanesulfonamide in pure form (1.06 g, 79%).

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후처리

  1. customThen, the mixture was quenched with 1N HCl
  2. extractionextracted with ethyl acetate (EtOAc)
  3. customDrying
  4. custom(MgSO4) and evaporation of the ethyl acetate
  5. customthe residue was purified by CC (eluent EtOAc/n-hexane)

출처 및 근거

ORD 기록
ord-ca39859f1b1f47f09ed664ed68c9e331
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946204B2

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