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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77728생성일: 2026년 10월 26일

Dichloromethane → 3-(6-Aminopyridin-2-yl)-4-methyl-N-[3-(trifloromethyl)phenyl]benzamide

https://huagongshe.com/reaction/77728

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참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Potassium CarbonateHCID 11430—
반응물2-Amino-6-bromopyridineHCID 300809—
반응물Potassium AcetateHCID 517044—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamideHCID 17197569—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-(6-Aminopyridin-2-yl)-4-methyl-N-[3-(trifloromethyl)phenyl]benzamideHCID 69047631—

반응 조건

온도85 °C

반응 단계

To a degassed mixture of 3-iodo-4-methyl-N-[3-(trifluoromethyl)phenyl]benzamide (0.500 g, 1.23 mmol), potassium acetate (424 mg, 4.32 mmol), DMF (15 mL), and 4,4,5,5,4′,4′,5′,5′-octamethyl-[2,2]bi[[1,3,2]dioxaborolanyl] (0.329 g, 1.30 mmol) was added [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II), complex with DCM (1:1) (101 mg, 0.123 mmol). The reaction was heated to 80° C. for 3 hours, at which time conversion to the boronic ester was complete. The mixture was cooled and potassium carbonate (512 mg, 3.70 mmol), water (2.24 mL), and 6-bromopyridin-2-amine (214 mg, 1.23 mmol) were added. After degassing the mixture, it was heated to 85° C. for 1 hour. The solvent was then removed in vacuo. Water was added and the product was extracted with three portions of ethyl acetate. The combined extracts were washed with brine, dried over sodium sulfate, and concentrated. Purification was carried out by flash column chromatography (eluting with a gradient from 0-50% ethyl acetate in hexanes) afforded the product. (254 mg, 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841318B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-fbb3af39a7c34521ab72c521080a6978
출처 메모uspto-grants-2014_09