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4-Methoxybenzenesulfonyl chloride → N-(3-Acetyl-2-hydroxyphenyl)-4-methoxybenzenesulfonamide

HRID 1603924
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HRID 1603924 반응식
Br.[NH2:2][C:3]1[C:4]([OH:12])=[C:5]([C:9](=[O:11])[CH3:10])[CH:6]=[CH:7][CH:8]=1.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1>N1C=CC=CC=1>[C:9]([C:5]1[C:4]([OH:12])=[C:3]([NH:2][S:21]([C:18]2[CH:17]=[CH:16][C:15]([O:14][CH3:13])=[CH:20][CH:19]=2)(=[O:23])=[O:22])[CH:8]=[CH:7][CH:6]=1)(=[O:11])[CH3:10]
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참가 물질

4

반응물 2

HCID 74014-Methoxybenzenesulfonyl chlorideHCID 196063433'-Amino-2'-hydroxyacetophenone hydrobromide

생성물 1

HCID 19606314N-(3-Acetyl-2-hydroxyphenyl)-4-methoxybenzenesulfonamide수율 83.4%

시약·촉매·용매 1

HCID 1049Pyridine용매2회

실험 절차

A solution of 3'-amino-2'-hydroxyacetophenone hydrobromide (1.282 g, 5.52 mmol) in pyridine (25 ml) was added at 0° C. with 4-methoxybenzenesulfonyl chloride (1.18 g, 5.71 mmol) dissolved in the minimum amount of pyridine and the mixture was left at room temperature for 18 h. Afterwards it was evaporated to dryness, redissolved in dichloromethane, washed with 1M HCl, dried and the solvent was evaporated off under reduced pressure, thereby obtaining 1.479 g of the title compound (81% yield).

후처리

  1. customAfterwards it was evaporated to dryness
  2. dissolutionredissolved in dichloromethane
  3. washwashed with 1M HCl
  4. customdried
  5. customthe solvent was evaporated off under reduced pressure

출처 및 근거

ORD 기록
ord-4776d61a27c64099be849b27e61d28a8
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05990142

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