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p-Bromobenzenesulfonyl chloride → 4-bromo-N-(2-pyridin-2-ylethyl)benzenesulfonamide

HRID 2103623
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HRID 2103623 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[N:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH2:18][CH2:19][NH2:20].C(N(CC)CC)C.C(=O)(O)[O-].[Na+]>ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:20][CH2:19][CH2:18][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][N:12]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 7396p-Bromobenzenesulfonyl chlorideHCID 8471TriethylamineHCID 759192-PyridineethanamineHCID 516892Sodium Bicarbonate

생성물 1

HCID 35270444-bromo-N-(2-pyridin-2-ylethyl)benzenesulfonamide수율 97.9%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매
2회

실험 절차

Add a solution of 4-bromo-benzenesulfonyl chloride (1.278 g, 5.0 mmol) in 10 mL dichloromethane at r.t. to a solution of 2-pyridin-2-yl-ethylamine (611 mg, 5.0 mmol) and triethylamine (708 μL, 5.0 mmol) in 5 mL dichloromethane over a period of 20 min via syringe pump and stir for 12 h. Add 20 mL saturated aqueous sodium bicarbonate solution and extract the aqueous phase with dichloromethane. Wash the combined organic extracts with brine, dry over sodium sulfate, filtrate and concentrate under reduced pressure to obtain 4-bromo-N-(2-pyridin-2-yl-ethyl)-benzenesulfonamide (1.67 g) as a pale yellow oil which slowly crystallizes upon storage at ambient temperature. Further purification is not necessary. MS (m/e): 342 (M+H).

후처리

  1. extractionextract the aqueous phase with dichloromethane
  2. washWash the combined organic extracts with brine
  3. dry with materialdry over sodium sulfate, filtrate
  4. concentrationconcentrate under reduced pressure

출처 및 근거

ORD 기록
ord-b2b1625b0c904ba4bb4cd2594d858549
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07576108B2

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