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Acetic Anhydride → Acetamide, N-(2-(4-chlorophenyl)ethyl)-N-(8-fluoro-4-quinolinyl)-

HRID 1196469
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인쇄 미리보기

반응식

HRID 1196469 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][NH:10][C:11]2[C:20]3[C:15](=[C:16]([F:21])[CH:17]=[CH:18][CH:19]=3)[N:14]=[CH:13][CH:12]=2)=[CH:4][CH:3]=1.[C:22](OC(=O)C)(=[O:24])[CH3:23]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][N:10]([C:11]2[C:20]3[C:15](=[C:16]([F:21])[CH:17]=[CH:18][CH:19]=3)[N:14]=[CH:13][CH:12]=2)[C:22](=[O:24])[CH3:23])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 1641804-Quinolinamine, N-(2-(4-chlorophenyl)ethyl)-8-fluoro-

생성물 1

HCID 164179Acetamide, N-(2-(4-chlorophenyl)ethyl)-N-(8-fluoro-4-quinolinyl)-

실험 절차

A mixture of 2.0 g of N-[2-(4-chlorophenyl)ethyl]-8-fluoro-4-quinolinamine and 5.0 mL of acetic anhydride was refluxed overnight. The mixture was then cooled, and solvents were removed by reducing pressure. The residue was washed with water and then dried. The resulting oil was passed over a silica gel column with ethyl acetate, and the front running spot was collected, producing 0.8 g of the title product as a thick oil.

후처리

  1. temperaturewas refluxed overnight
  2. temperatureThe mixture was then cooled
  3. customsolvents were removed
  4. washThe residue was washed with water
  • customdried
  • customwas collected
  • 출처 및 근거

    ORD 기록
    ord-76a3137aaf214e2984966b49ea48ad33
    출처 데이터셋
    uspto-grants-1992_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05114939

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