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O-Toluidine → 3-Acetyl-4-(2-methylphenylamino)-8-methoxyquinoline

HRID 1382308
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반응식

HRID 1382308 반응식
[C:1]([C:4]1[CH:5]=[N:6][C:7]2[C:12]([C:13]=1Cl)=[CH:11][CH:10]=[CH:9][C:8]=2[O:15][CH3:16])(=[O:3])[CH3:2].[NH2:17][C:18]1[C:19]([CH3:24])=[CH:20][CH:21]=[CH:22][CH:23]=1>O1CCOCC1>[C:1]([C:4]1[CH:5]=[N:6][C:7]2[C:12]([C:13]=1[NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[CH3:24])=[CH:11][CH:10]=[CH:9][C:8]=2[O:15][CH3:16])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7242O-ToluidineHCID 100143133-Acetyl-4-chloro-8-methoxyquinoline

생성물 1

HCID 104704093-Acetyl-4-(2-methylphenylamino)-8-methoxyquinoline수율 45.5%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A mixture of crude 3-acetyl-4-chloro-8-methoxyquinoline (7.9 g) and o-toluidine (2 ml, 19 mmol) in dioxan (150 ml) was heated under reflux with stirring for 2 hours, then cooled and evaporated. Aqueous sodium bicarbonate was added, the mixture extracted with chloroform, and the organic extract dried and evaporated. Recrystallisation from ethyl acetate and then from ethanol gave 3-acetyl-4-(2-methylphenylamino)-8-methoxyquinoline (2.65 g, 44% from 3-acetyl-8-methoxy-4(1H)-quinolone), m.p. 171°-173°.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux
  3. temperaturecooled
  4. customevaporated
  5. additionAqueous sodium bicarbonate was added
  6. extractionthe mixture extracted with chloroform
  7. extractionthe organic extract
  8. customdried
  9. customevaporated
  10. customRecrystallisation from ethyl acetate

출처 및 근거

ORD 기록
ord-c48f1d25b087454ebb7a5edd3937a0aa
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04806550

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