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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446314생성일: 2026년 10월 26일

Binap, (A+-)- → Ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/446314

반응식

참여 물질

역할이름HCID투입량
반응물Binap, (A+-)-HCID 634876—
반응물4-(2-Chloropyridin-3-yl)pyrimidineHCID 16108974—
반응물Ethyl 3-amino-4-(trifluoromethyl)benzoateHCID 19783159—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoateHCID 66970285—

반응 조건

온도80 °C

반응 단계

4-(2-Chloropyridin-3-yl)pyrimidine (1.5 g, 7.8 mmol), ethyl 3-amino-4-(trifluoromethyl)benzoate (2.0 g, 8.6 mmol), Sodium tert-butoxide (1.1 g, 12 mmol), rac-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (0.49 g, 0.78 mmol) were all mixed together in toluene (25 ml) and degassed under vacuum. Nitrogen was bubbled into the reaction for 5 minutes and then Palladium (II) acetate (0.088 g, 0.39 mmol) was added. The mixture was heated to 80° C. and stirred overnight. The reaction was diluted with ethyl acetate and washed with an aqueous saturated solution of sodium bicarbonate, water and brine. The organic layer was then dried with sodium sulfate and purified by column chromatography on silica gel using a gradient 5 to 40% ethyl acetate in hexanes to afford ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoate as a brown solid. MS m/z=389 [M+1]+. Calc'd for C19H15F3N4O2: 388.11.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08476434B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-f176647a0d194514a51ae28998697137
출처 메모uspto-grants-2013_07