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N-[2-(3,4-dimethoxyphenyl)-1-(3-pyridyl)ethyl]benzamide → 3,4-Dihydro-6,7-dimethoxy-1-phenyl-3-(3-pyridyl)isoquinoline

HRID 464317
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인쇄 미리보기

반응식

HRID 464317 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH:12]([NH:19][C:20](=O)[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]>P(Cl)(Cl)(Cl)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:6](=[CH:7][C:8]=1[O:9][CH3:10])[C:20]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[N:19][CH:12]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1)[CH2:11]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 13319894N-[2-(3,4-dimethoxyphenyl)-1-(3-pyridyl)ethyl]benzamide

생성물 1

HCID 133198953,4-Dihydro-6,7-dimethoxy-1-phenyl-3-(3-pyridyl)isoquinoline수율 93.5%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

실험 절차

1.8 g of N-[2-(3,4-dimethoxyphenyl)-1-(3-pyridyl)ethyl]benzamide in 20 ml of phosphorus oxychloride are stirred at 60° C. for 5 hours and at 120° C. for 1.5 hours. The yellow precipitate is filtered off with suction, dissolved in 200 ml of water, and the solution is made alkaline with potassium carbonate and extracted twice with methylene chloride. 1.6 g of dihydroisoquinoline compound of melting point 180°-182° C. are isolated.

후처리

  • filtrationThe yellow precipitate is filtered off with suction
  • dissolutiondissolved in 200 ml of water
  • extractionextracted twice with methylene chloride
  • 출처 및 근거

    ORD 기록
    ord-57df71bd4f8f4d54b0aca8c2d3e9d4c5
    출처 데이터셋
    uspto-grants-1985_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04547508

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