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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Binap, (A+-)- | HCID 634876 | — |
| 반응물 | 4-(2-Chloropyridin-3-yl)pyrimidine | HCID 16108974 | — |
| 반응물 | Ethyl 3-amino-4-(trifluoromethyl)benzoate | HCID 19783159 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoate | HCID 66970285 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08476434B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-f176647a0d194514a51ae28998697137 |
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| 출처 메모 | uspto-grants-2013_07 |
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