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Methylamine → N-(3-fluoro-4-methylsulfamoylphenyl)acetamide

HRID 407287
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반응식

HRID 407287 반응식
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11](Cl)(=[O:13])=[O:12])=[C:7]([F:15])[CH:6]=1)(=[O:3])[CH3:2].[CH3:16][NH2:17]>ClCCl.C1COCC1>[F:15][C:7]1[CH:6]=[C:5]([NH:4][C:1](=[O:3])[CH3:2])[CH:10]=[CH:9][C:8]=1[S:11](=[O:13])(=[O:12])[NH:17][CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6329MethylamineHCID 167710844-Acetamido-2-fluorobenzene-1-sulfonyl chloride

생성물 1

HCID 34029456N-(3-fluoro-4-methylsulfamoylphenyl)acetamide수율 79%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매

실험 절차

The above prepared 4-acetylamino-2-fluorobenzenesulfonyl chloride (2 g, 7.9 mmol) was dissolved in dichloromethane and methylamine (9.9 mL of a 2M solution in THF, 19.9 mmol) was added. The reaction was stirred at room temperature for 2 hrs. The solvent was then evaporated under reduced pressure and the resulting solid was suspended in 50 mL of water. The solid was isolated by filtration and dried to yield 1.55 g (79%) of N-(3-fluoro-4-methylsulfamoylphenyl)acetamide which was used in the subsequent step without further purification.

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후처리

  1. customThe solvent was then evaporated under reduced pressure
  2. customThe solid was isolated by filtration
  3. customdried

출처 및 근거

ORD 기록
ord-184cd5ef139e4bb098f833d77484554a
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754233B2

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