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2-Phenylbenzene-1-sulfonyl chloride → N-(4-Chloro-3-methyl-5-isoxazolyl)-2-biphenylsulfonamide

HRID 1167015
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반응식

HRID 1167015 반응식
[NH2:1][C:2]1[O:6][N:5]=[C:4]([CH3:7])[C:3]=1[Cl:8].[C:9]1([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:10]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:12]=[CH:13][CH:14]=1>>[Cl:8][C:3]1[C:4]([CH3:7])=[N:5][O:6][C:2]=1[NH:1][S:15]([C:10]1[C:9]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 27566802-Phenylbenzene-1-sulfonyl chlorideHCID 105828224-Chloro-3-methyl-1,2-oxazol-5-amine

생성물 1

HCID 15453178N-(4-Chloro-3-methyl-5-isoxazolyl)-2-biphenylsulfonamide수율 74%

실험 절차

N-(4-Chloro-3-methyl-5-isoxazolyl)-2-biphenylsulfonamide was prepared in the same manner as described in Example 202 from 5-amino-4-chloro-3-methylisoxazole and 2-biphenylsulfonyl chloride in 74% yield. Purification was achieved by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 132-134° C.

후처리

  1. customPurification
  2. customwas achieved by recrystallization from ethyl acetate/hexanes
  3. customto give a crystalline solid, m.p. 132-134° C.
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

출처 및 근거

ORD 기록
ord-f70cac315e094391bf3e50e91fbea569
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06613804B2

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