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Dichloromethane → 1,4-Dihydro-3-methoxymethyl-5-methyl-8-nitro-4-oxoquinoline

HRID 613565
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인쇄 미리보기

반응식

HRID 613565 반응식
[OH:1][CH2:2][C:3]1[C:12](=[O:13])[C:11]2[C:6](=[C:7]([N+:15]([O-:17])=[O:16])[CH:8]=[CH:9][C:10]=2[CH3:14])[NH:5][CH:4]=1.S(Cl)(Cl)=O.Cl[CH2:23]Cl>>[CH3:23][O:1][CH2:2][C:3]1[C:12](=[O:13])[C:11]2[C:6](=[C:7]([N+:15]([O-:17])=[O:16])[CH:8]=[CH:9][C:10]=2[CH3:14])[NH:5][CH:4]=1
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참가 물질

4

반응물 3

HCID 6344Dichloromethane2회HCID 24386Thionyl ChlorideHCID 195924831,4-Dihydro-3-hydroxymethyl-5-methyl-8-nitro-4-oxoquinoline

생성물 1

HCID 195923511,4-Dihydro-3-methoxymethyl-5-methyl-8-nitro-4-oxoquinoline

실험 절차

To a suspension of 1,4-dihydro-3-hydroxymethyl-5-methyl-8-nitro-4-oxoquinoline (1.12 g) in dichloromethane (10 ml) was dropwise added a solution of thionyl chloride (569 mg) in dichloromethane (5 ml) under ice-cooling, and the mixture was stirred for 1 hour at the same temperature and for 2 hours at ambient temperature. The mixture was concentrated in vacuo, suspended in dichloromethane-methanol and refluxed for 2 hours. The mixture was evaporated in vacuo, and the residue was recrystalized from methanol to give 1,4-dihydro-3-methoxymethyl-5-methyl-8-nitro-4-oxoquinoline (889 mg).

후처리

  1. temperaturecooling
  2. concentrationThe mixture was concentrated in vacuo
  3. temperaturerefluxed for 2 hours
  4. customThe mixture was evaporated in vacuo
  5. customthe residue was recrystalized from methanol

출처 및 근거

ORD 기록
ord-95f2cf7a6b9d4cbdad2eb0d93b8ffbf2
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06008230

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