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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 750164생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/750164

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물Methylboronic AcidHCID 139377—
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-methyl-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 4445188281.8%

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), methylboronic acid (200 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 the residue was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-hexane:ethyl acetate=2:1) and recrystallized (ethyl acetate-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-29f70d52716844d78fe6ef402124206c
출처 메모uspto-grants-2008_07