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5-(benzyloxy)-1-biphenyl-3-yl-2-methylpyridin-4(1H)-one → 1-biphenyl-3-yl-5-hydroxy-2-methylpyridin-4(1H)-one

HRID 1056899
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반응식

HRID 1056899 반응식
C([O:8][C:9]1[C:10](=[O:28])[CH:11]=[C:12]([CH3:27])[N:13]([C:15]2[CH:16]=[C:17]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:18]=[CH:19][CH:20]=2)[CH:14]=1)C1C=CC=CC=1>Cl>[C:17]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:18]=[CH:19][CH:20]=[C:15]([N:13]2[CH:14]=[C:9]([OH:8])[C:10](=[O:28])[CH:11]=[C:12]2[CH3:27])[CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 674193565-(benzyloxy)-1-biphenyl-3-yl-2-methylpyridin-4(1H)-one

생성물 1

HCID 674185551-biphenyl-3-yl-5-hydroxy-2-methylpyridin-4(1H)-one

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

반응 조건

온도
140 °C

실험 절차

6.0 g (1.3 mmol) 5-(benzyloxy)-1-biphenyl-3-yl-2-methyipyridin-4(1H)-one was suspended 150 ml 4 N aq HCl. The reaction mixture was heated at 140° C. for 18 h, then cooled to rt, concentrated in vacuo, suspended in CH2C 2, and collected by filtration to give 1-biphenyl-3-yl-5-hydroxy-2-methylpyridin-4(1/-/)-one. LCMS (M+H)+=278.2.

후처리

  • temperaturecooled to rt
  • concentrationconcentrated in vacuo
  • filtrationcollected by filtration
  • 출처 및 근거

    ORD 기록
    ord-de1233cf486d4f438187ed30d867fd37
    출처 데이터셋
    uspto-grants-2016_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09399651B2

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