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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130644생성일: 2026년 10월 25일

Dimethylformamide → 3',4'-difluoro-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)biphenyl-4-carboxamide

https://huagongshe.com/reaction/130644

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium CarbonateHCID 10340—
반응물3,4-Difluorobenzeneboronic acidHCID 2734337—
반응물N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)-4-iodobenzamideHCID 59731034—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물3',4'-difluoro-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)biphenyl-4-carboxamideHCID 5973103854.7%

반응 조건

온도80 °C

반응 단계

Next, to a solution of N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)-4-iodobenzamide (100 mg, 0.25 mmol) in a 3 to 1 mixture of DMF and H2O was added 3,4-difluorophenylboronic acid (80.3 mg, 0.51 mmol), tetrakis(triphenylphosphine)palladium(0) (8.82 mg, 0.01 mmol), and sodium carbonate (80.9 mg, 0.76 mmol). The mixture was stirred at 80° C. for 2.5 hours, and after cooled to room temperature, the product was extracted with diethyl ether. The organic layer was washed with water then brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. After triturated with ethylacetate and hexane, the solid was filtered to afford 3′,4′-difluoro-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)biphenyl-4-carboxamide (51.9 mg, 54%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381840B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-a52936f01c8741b6a6197647ecdb7c82
출처 메모uspto-grants-2008_06