HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42003Erstellt: 26. Oktober 2026
Binap, (A+-)- → tert-Butyl 2-(6-bromopyridin-3-ylamino)-5-methylbenzoate
https://huagongshe.com/reaction/42003
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 2-Bromo-5-iodopyridine | HCID 4738271 | — |
| Edukt | tert-Butyl 2-amino-5-methylbenzoate | HCID 13399998 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | tert-Butyl 2-(6-bromopyridin-3-ylamino)-5-methylbenzoate | HCID 86657255 | 40,2% |
Reaktionsschritte
In a schlenck tube, a mixture of tert-butyl 2-amino-5-methylbenzoate (2.89 mmol, 0.600 g), 2-bromo-5-iodopyridine (2.89 mmol, 0.822 g), BINAP (0.29 mmol, 0.096 g), Pd2(dba)3 (0.14 mmol, 0.132 g) and NaOtBu (5.79 mmol, 0.556 g) in toluene (15 ml) was heated at 120° C. for 3 hours. Water and ethyl acetate were added to the reaction crude. The aqueous phase was extracted again with more ethyl acetate. The organic phase was washed with water and brine, dried, filtered and concentrated in vacuo. The crude mixture was purified by chromatography (Biotage 40S, SiO2, Hexane:Ethyl acetate from 0% to 10%) affording 0.422 g (yield 40%) of the expected product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536165B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-526c59565f6c4553ab53563a4218665a |
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| Quellennotiz | uspto-grants-2013_09 |
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