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Chlorine monoxide → 4-Chloro-8-methoxyquinoline-3-carbonitrile

HRID 1935094
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HRID 1935094 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[NH:11][CH:10]=[C:9]([C:13]#[N:14])[C:8]2=O.O(Cl)[Cl:17]>CN(C=O)C>[Cl:17][C:8]1[C:7]2[C:12](=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][CH:6]=2)[N:11]=[CH:10][C:9]=1[C:13]#[N:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24646Chlorine monoxideHCID 22466766HCID 22466766, 화합물

생성물 1

HCID 224666994-Chloro-8-methoxyquinoline-3-carbonitrile수율 91%

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

실험 절차

A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy -3-quinolinecarbonitrile as an off white solid in 91% yield, mass spectrum (electrospray, m/e): M+H 219.1.

후처리

  1. temperaturewas refluxed for 0.5 hours
  2. customThe mixture was evaporated to dryness
  3. additiondiluted with hexanes
  4. customThe solid was collected
  5. additionmixed with cold dilute sodium carbonate solution
  6. extractionextracted several times with ethyl acetate
  7. dry with materialThe organic layer was dried over sodium sulfate
  8. filtrationfiltered through a pad of silica gel
  9. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-bd146f0376ec482e9149f67e0d603b8d
출처 데이터셋
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06384051B1

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