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Dimethylformamide → Ethyl 6-chloro-2-methylquinoline-3-carboxylate

HRID 2187666
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HRID 2187666 반응식
[CH3:1]N(C=O)C.P(Cl)(Cl)(Cl)=O.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][C:19]([CH3:26])=[CH:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:14][CH:13]=1>ClCCCl>[Cl:11][C:12]1[CH:13]=[C:14]2[C:15](=[CH:16][CH:17]=1)[N:18]=[C:19]([CH3:26])[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:1]2
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 38739Ethyl 3-(4-chloroanilino)but-2-enoate

생성물 1

HCID 11288138Ethyl 6-chloro-2-methylquinoline-3-carboxylate

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매2회

실험 절차

To a solution of 6.2 g (83 mmol) DMF in 50 ml of 1,2 dichloroethane was carefully added 19.1 g (126 mmol) of phosphoryl chloride. After stirring for 10 min at ambient temperature a solution of 20 g (83 mol) of ethyl 3-(4-chlorophenylamino)but-2-enoate in 50 ml of 1,2 dichloroethane was added slowly, while the mixture turned dark in an exothermic reaction. Stirring at ambient temperature was continued for another hour followed by heating with reflux for 6 h. The mixture was poured on to crushed ice, washed twice with water, dried over sodium sulfate, and concentrated under reduced pressure. The title ester was obtained from the residue via flash chromatography on silica gel with dichloromethane/hexane 4:1.

후처리

  1. additionwas added slowly, while the mixture
  2. customturned dark in an exothermic reaction
  3. waitwas continued for another hour
  4. temperatureby heating
  5. temperaturewith reflux for 6 h
  6. additionThe mixture was poured on
  7. customto crushed ice
  8. washwashed twice with water
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-791b847c980d42218141872d67865483
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410562B1

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