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Diphenyl Ether → Ethyl 6-iodo-4-oxo-1,4-dihydro-3-quinolinecarboxylate

HRID 230836
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인쇄 미리보기

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HRID 230836 반응식
C1(OC2C=CC=CC=2)C=CC=CC=1.[I:14][C:15]1[CH:20]=[CH:19][C:18]([NH:21][CH:22]=[C:23]([C:29]([O:31]CC)=O)[C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:17][CH:16]=1>CC(CCC)C>[I:14][C:15]1[CH:16]=[C:17]2[C:18](=[CH:19][CH:20]=1)[NH:21][CH:22]=[C:23]([C:24]([O:26][CH2:27][CH3:28])=[O:25])[C:29]2=[O:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7583Diphenyl EtherHCID 4026452Diethyl 2-((4-iodophenylamino)methylene)malonate

생성물 1

HCID 719682Ethyl 6-iodo-4-oxo-1,4-dihydro-3-quinolinecarboxylate

시약·촉매·용매 1

HCID 78922-Methylpentane용매

실험 절차

Diphenyl ether (175 ml) was heated to reflux temperature, and Intermediate 10 was gradually added down an air condenser. Once all the reagent had been added the mixture was heated under reflux for a further 30 min. The mixture was then cooled and 2-methylpentane (200 ml) was added. The solid formed was collected by filtration to give the title compound (24.6 g).

후처리

  1. additionwas gradually added down an air condenser
  2. additionOnce all the reagent had been added the mixture
  3. temperaturewas heated
  4. temperatureunder reflux for a further 30 min
  5. temperatureThe mixture was then cooled
  6. customThe solid formed
  7. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-54a385256a874b199dd6d9b03ea3d8d9
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07566786B2

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