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Hydrochloric Acid → (E)-4-[2-[2-[[(p-Methoxyphenyl)sulfonyl]amino]phenyl]ethenyl]pyridine Hydrochloride

HRID 1741017
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인쇄 미리보기

반응식

HRID 1741017 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2/[CH:19]=[CH:20]/[C:21]2[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=2)(=[O:11])=[O:10])=[CH:5][CH:4]=1.[ClH:27]>CO>[ClH:27].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([S:9]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2/[CH:19]=[CH:20]/[C:21]2[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=2)(=[O:11])=[O:10])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 6366736Hmn 154

생성물 1

HCID 21834473(E)-4-[2-[2-[[(p-Methoxyphenyl)sulfonyl]amino]phenyl]ethenyl]pyridine Hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

One (1.00) compound obtained in Example 3A was dissolved in 100 ml of methanol followed by addition of hydrogen chloride gas-saturated ethereal solution of 5 times as much by volume under ice-cooling. The solvent was then evaporated off to provide 1.07 g of the title compound as yellow powders. m.p. 258-261° C. (decomp.)

후처리

  • temperaturecooling
  • customThe solvent was then evaporated off
  • 출처 및 근거

    ORD 기록
    ord-f98c8cbec7424563b3f797c846a5c24e
    출처 데이터셋
    uspto-grants-1999_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05972976

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