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4-Toluenesulfonyl chloride → N-{5-[(4-methoxybenzyl)oxy]pyridin-2-yl}-4-methylbenzenesulfonamide

HRID 2095832
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인쇄 미리보기

반응식

HRID 2095832 반응식
[CH3:1][O:2][C:3]1[CH:17]=[CH:16][C:6]([CH2:7][O:8][C:9]2[CH:10]=[CH:11][C:12]([NH2:15])=[N:13][CH:14]=2)=[CH:5][CH:4]=1.[CH3:18][C:19]1[CH:24]=[CH:23][C:22]([S:25](Cl)(=[O:27])=[O:26])=[CH:21][CH:20]=1>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][O:8][C:9]2[CH:10]=[CH:11][C:12]([NH:15][S:25]([C:22]3[CH:23]=[CH:24][C:19]([CH3:18])=[CH:20][CH:21]=3)(=[O:27])=[O:26])=[N:13][CH:14]=2)=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 73974-Toluenesulfonyl chlorideHCID 284910055-((4-Methoxybenzyl)oxy)pyridin-2-amine

생성물 1

HCID 66968540N-{5-[(4-methoxybenzyl)oxy]pyridin-2-yl}-4-methylbenzenesulfonamide수율 93%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 5-[(4-methoxybenzyl)oxy]pyridin-2-amine (24 g, 104 mmol) in pyridine (210 mL) was added 4-methylbenzenesulfonyl chloride (20.9 g, 110 mmol) at 0° C., and the mixture was stirred at room temperature for 4 hr. The reaction mixture was concentrated, the residue was washed with saturated aqueous sodium hydrogen carbonate solution and ethyl acetate to give the title compound (37 g, 93%) as a pale-red solid.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. washthe residue was washed with saturated aqueous sodium hydrogen carbonate solution and ethyl acetate

출처 및 근거

ORD 기록
ord-c7aaf62766c943bb8e585406c76afb44
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08445509B2

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