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

HRID 1428769
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인쇄 미리보기

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HRID 1428769 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH2:9])=[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:7]=[CH:6][C:5]([CH2:8][NH:9][S:13]([CH2:11][CH3:12])(=[O:15])=[O:14])=[C:4]([F:10])[CH:3]=1
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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

반응 조건

온도
0 °C

실험 절차

(4-Bromo-2-fluorophenyl)methanamine (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. Drying over magnesium sulfate and evaporation of the ethyl acetate and purified by column chromatography gave N-(4-bromo-2-fluorobenzyl)-ethanesulfonamide in pure form (1.06 g, 79%).

후처리

  1. customThen, the mixture was quenched with 1N HCl
  2. extractionextracted with ethyl acetate
  3. dry with materialDrying over magnesium sulfate and evaporation of the ethyl acetate
  4. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-4ad33e7a18a64304ac8b533d122f3afb
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08937092B2

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