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HRID 446314作成日:2026年10月27日

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

https://huagongshe.com/reaction/446314

反応式

関与物質

役割名称HCID仕込み量
反応物Binap, (A+-)-HCID 634876—
反応物4-(2-Chloropyridin-3-yl)pyrimidineHCID 16108974—
反応物Ethyl 3-amino-4-(trifluoromethyl)benzoateHCID 19783159—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoateHCID 66970285—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08476434B2
出典データセットuspto-grants-2013_07
ORD IDord-f176647a0d194514a51ae28998697137
出典メモuspto-grants-2013_07