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Triethylamine → 5-bromo-2-methoxy-N-methylbenzenesulfonamide

HRID 531438
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HRID 531438 반응식
Cl.CN.[CH2:4]([N:6](CC)CC)C.[Br:11][C:12]1[CH:13]=[CH:14][C:15]([O:22][CH3:23])=[C:16]([S:18](Cl)(=[O:20])=[O:19])[CH:17]=1>C(Cl)Cl>[Br:11][C:12]1[CH:13]=[CH:14][C:15]([O:22][CH3:23])=[C:16]([S:18]([NH:6][CH3:4])(=[O:20])=[O:19])[CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 5200205-Bromo-2-methoxybenzene-1-sulfonyl chlorideHCID 6364545Methylamine hydrochloride

생성물 1

HCID 84680955-bromo-2-methoxy-N-methylbenzenesulfonamide수율 81.63%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a stirred ice cold mixture of methylamine hydrochloride (231.1 mg, 3.5 mmol), triethylamine (1.26 mL, 8.755 mmol) in DCM was added a solution of 5-bromo-2-methoxybenzene-1-sulfonyl chloride (500 mg, 1.751 mmol) in DCM at 0° C. This was stirred at RT for three hours. This mixture was then poured on to ice cold water and extracted with DCM, dried over sodium sulfate and concentrated to get 400 mg (81.63% yield) of titled compound.

후처리

  1. additionThis mixture was then poured on to ice cold water
  2. extractionextracted with DCM
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a6df682d67b54c1591f8da11e2e9de8e
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353107B2

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