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Water → N-(5-bromopyridin-3-yl)benzenesulfonamide

HRID 537728
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인쇄 미리보기

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HRID 537728 반응식
[NH2:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Br:8])[CH:7]=1.[C:9]1([S:15](Cl)(=[O:17])=[O:16])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.O>N1C=CC=CC=1>[Br:8][C:6]1[CH:7]=[C:2]([NH:1][S:15]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)(=[O:17])=[O:16])[CH:3]=[N:4][CH:5]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 7369Benzenesulfonyl chlorideHCID 8176813-Amino-5-bromopyridine

생성물 1

HCID 57843412N-(5-bromopyridin-3-yl)benzenesulfonamide수율 100%

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
20 °C

실험 절차

To a solution of 3-amino-5-bromopyridine (0.500 g, 2.89 mmol) in pyridine (2 mL) was added benzenesulfonyl chloride (0.404 mL, 3.18 mmol) dropwise. The reaction mixture was stirred at room temperature (20° C.) for 16 h. After this time, water (5 mL) was added to the reaction mixture. The resulting crystalline solid was collected by filtration, washed with water and dried in the vacuum oven to afford the title compound (0.898 g, 2.89 mmol, quantitative). No further purification was required.

후처리

  1. filtrationThe resulting crystalline solid was collected by filtration
  2. washwashed with water
  3. customdried in the vacuum oven

출처 및 근거

ORD 기록
ord-2630d4cf971a4fcf80fd558e8ddc669c
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865699B2

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