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2-Fluoro-benzoic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide → 3-benzenesulfonylmethyl-5-(2-fluoro-phenyl)-1H-[1,2,4]triazole

HRID 277105
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인쇄 미리보기

반응식

HRID 277105 반응식
[NH2:1][C:2](=[N:13][NH:14][C:15](=O)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[F:22])[CH2:3][S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:6])=[O:5]>C(O)C>[C:7]1([S:4]([CH2:3][C:2]2[N:1]=[C:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[F:22])[NH:14][N:13]=2)(=[O:6])=[O:5])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 867578502-Fluoro-benzoic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide

생성물 1

HCID 1785273973-benzenesulfonylmethyl-5-(2-fluoro-phenyl)-1H-[1,2,4]triazole수율 86%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

14 g (0.042 mol) 2-fluoro-benzoic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide were heated at 210° C. for 20 minutes. The molten mass was then cooled, dissolved in 40 ml hot ethanol and stirred overnight at room temperature. The precipitated crystals were filtered off and dried to yield 11.4 g (86%) 3-benzenesulfonylmethyl-5-(2-fluoro-phenyl)-1H-[1,2,4]triazole as beige solid, MS m/e (%): 317 (M+, 2), 253(68), 176(100), 122(61).

후처리

  • temperatureThe molten mass was then cooled
  • filtrationThe precipitated crystals were filtered off
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-25b06decc91e405c987ea5616c2a91d3
    출처 데이터셋
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06355653B1

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