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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt2-Bromo-5-iodopyridineHCID 4738271—
Edukttert-Butyl 2-amino-5-methylbenzoateHCID 13399998—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl 2-(6-bromopyridin-3-ylamino)-5-methylbenzoateHCID 8665725540,2%

Reaktionsbedingungen

Temperatur120 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536165B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-526c59565f6c4553ab53563a4218665a
Quellennotizuspto-grants-2013_09