HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 446314Erstellt: 25. Oktober 2026
Binap, (A+-)- → Ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/446314
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 4-(2-Chloropyridin-3-yl)pyrimidine | HCID 16108974 | — |
| Edukt | Ethyl 3-amino-4-(trifluoromethyl)benzoate | HCID 19783159 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Ethyl 3-(3-(pyrimidin-4-yl)pyridin-2-ylamino)-4-(trifluoromethyl)benzoate | HCID 66970285 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08476434B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-f176647a0d194514a51ae28998697137 |
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| Quellennotiz | uspto-grants-2013_07 |
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