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Ethanol → 1-(4-Fluorophenyl)-1,4-di-hydro4-oxo-7-(4-pyridinyl)-3-quinolinecarboxylic acid

HRID 1032716
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반응식

HRID 1032716 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:17]3[C:12](=[CH:13][CH:14]=[C:15]([C:18]4[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=4)[CH:16]=3)[C:11](=[O:24])[C:10]([C:25]([O:27]CC)=[O:26])=[CH:9]2)=[CH:4][CH:3]=1.[OH-].[K+].C(O)C>C(O)(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:17]3[C:12](=[CH:13][CH:14]=[C:15]([C:18]4[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=4)[CH:16]=3)[C:11](=[O:24])[C:10]([C:25]([OH:27])=[O:26])=[CH:9]2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 10023142Ethyl 1-(4-fluorophenyl)1,4-dihydro-4-oxo-7-(4-pyridinyl)-3-quinolinecarboxylate

생성물 1

HCID 103385501-(4-Fluorophenyl)-1,4-di-hydro4-oxo-7-(4-pyridinyl)-3-quinolinecarboxylic acid수율 100.1%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 2.8 g of ethyl 1-(4-fluorophenyl)1,4 -dihydro-4-oxo-7-(4-pyridinyl)-3-quinolinecarboxylate, 20 ml of 10% potassium hydroxide solution and 10 ml ethanol was heated on a steam bath for 3 hrs. The reaction mixture was cooled and acidified with acetic acid. The solid product was collected and washed with acetone to give 2.6 g 1-(4-fluorophenyl)-1,4-dihydro-4-oxo-7-(4-pyridinyl)-3-quinolinecarboxylic acid. A sample of the compound was converted to its monomethanesulfonate salt, m.p. 280-281° C. when recrystallized from acetonitrile.

후처리

  1. temperaturewas heated on a steam bath for 3 hrs
  2. temperatureThe reaction mixture was cooled
  3. customThe solid product was collected
  4. washwashed with acetone

출처 및 근거

ORD 기록
ord-5a004ab8773144f9ac7ad6412473c887
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04959363

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