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2-Bromoethanol → 3-Isobutyryl-4-(2-methylphenylamino)-8-(2-hydroxyethoxy)-quinoline

HRID 1534496
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HRID 1534496 반응식
[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[CH3:23])=[CH:13][CH:12]=[CH:11][C:10]=2[OH:24])(=[O:5])[CH:2]([CH3:4])[CH3:3].[CH3:25][C:26](C)([O-:28])C.[K+].BrCCO>O1CCCC1>[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[CH3:23])=[CH:13][CH:12]=[CH:11][C:10]=2[O:24][CH2:25][CH2:26][OH:28])(=[O:5])[CH:2]([CH3:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 108982-Bromoethanol2회HCID 103586453-Isobutyryl-4-(2-methylphenylamino) 8-hydroxyquinolineHCID 23665647Potassium tert-butoxide2회

생성물 1

HCID 104064693-Isobutyryl-4-(2-methylphenylamino)-8-(2-hydroxyethoxy)-quinoline수율 39.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 3-isobutyryl-4-(2-methylphenylamino)-8-hydroxyquinoline (5 g, 15.6 mmol) in dry tetrahydrofuran (250 ml) was added potassium t-butoxide (2.63 g, 23.4 mmol), followed by 2-bromoethanol (3.9 g, 31.2 mmol). The stirred mixture was heated under reflux for 16 hours, then a further quantity of potassium t-butoxide (2.63 g, 23.4 mmol) and 2-bromoethanol (3.9 g, 31.2 mmol) added, and heating continued for 2 days. The solvent was evaporated, and the residue treated with aqueous sodium bicarbonate and extracted into dichloromethane. The extracts were dried and evaporated to an oil, which was purified by flash chromatography (silica gel, dichloromethane/methanol) and recrystallization from 40-60 petroleum ether to yield 3-isobutyryl-4-(2-methylphenylamino)-8-(2-hydroxyethoxy)-quinoline (2.25 g), m.p. 154°-156°.

후처리

  1. temperatureThe stirred mixture was heated
  2. temperatureunder reflux for 16 hours
  3. temperatureheating
  4. customThe solvent was evaporated
  5. additionthe residue treated with aqueous sodium bicarbonate
  6. extractionextracted into dichloromethane
  7. customThe extracts were dried
  8. customevaporated to an oil, which
  9. customwas purified by flash chromatography (silica gel, dichloromethane/methanol) and recrystallization from 40-60 petroleum ether

출처 및 근거

ORD 기록
ord-affdba173dad490f957f0361d0024645
출처 데이터셋
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05089504

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