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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 750165생성일: 2026년 10월 24일

Toluene → 2-benzyl-6-butyl-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl Ester

https://huagongshe.com/ko/reaction/750165

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물Butylboronic AcidHCID 20479—
반응물2-benzyl-6-bromo-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 44451690—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-benzyl-6-butyl-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 4445185073.7%

반응 조건

온도100 °C

반응 단계

A mixture of 2-benzyl-6-bromo-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester (300 mg), n-butylboronic acid (340 mg), tetrakis(triphenylphosphine)palladium(0) (80 mg), potassium carbonate (280 mg), toluene (6 ml) and THF (3 ml) was stirred at 100° C. under a nitrogen atmosphere for 12 hrs. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine. The solvent was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-hexane:ethyl acetate=2:1) and crystallized from hexane to give the title compound (210 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402595B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-aabba87175394c2c8a5369dc6e20589b
출처 메모uspto-grants-2008_07