Potassium Carbonate → Methyl 6-(4-methylphenyl)-2-methylquinoline-3-carboxylate

HRID 566032노트

반응식

HRID 566032 반응식
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([CH3:12])[C:6]([C:13]([O:15][CH3:16])=[O:14])=[CH:5]2.B([O-])([O-])O[C:19]1[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C(CCO)=CC=CC=1.O>[CH3:25][C:22]1[CH:23]=[CH:24][C:19]([C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[N:8]=[C:7]([CH3:12])[C:6]([C:13]([O:15][CH3:16])=[O:14])=[CH:5]3)=[CH:20][CH:21]=1

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 18472460Methyl 6-bromo-2-methylquinoline-3-carboxylateHCID 866453334-Methylphenyl borate

생성물 1

HCID 18472437Methyl 6-(4-methylphenyl)-2-methylquinoline-3-carboxylate수율 100.6%

시약·촉매·용매 1

HCID 66602552Toluene-ethanol water용매

실험 절차

Under argon atmosphere, a solution of methyl 6-bromo-2-methylquinoline-3-carboxylate (1.22 g), 4-methylphenyl borate (0.65 g) and potassium carbonate (1.18 g) in toluene-ethanol-water (40-4-4 ml) was stirred at room temperature for 1 hour. To the reaction mixture was added tetrakis-triphenylphosphinepalladium (0.15 g), and the mixture was refluxed for 18 hours and cooled to room temperature. The organic layer was washed with saturated sodium chloride solution, dried with magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:1) to give methyl 6-(4-methylphenyl)-2-methylquinoline-3-carboxylate (1.27 g) as colorless crystals.

후처리

  1. temperaturethe mixture was refluxed for 18 hours
  2. washThe organic layer was washed with saturated sodium chloride solution
  3. dry with materialdried with magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was separated
  6. custompurified with column chromatography (ethyl acetate/hexane=1:1)

출처 및 근거

ORD 기록
ord-cf90bc6a48794b23b7bfac64e36fe3de
출처 데이터셋
uspto-grants-2001_01
특허 번호
US06172061B2

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