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HRID 253115Erstellt: 23. Oktober 2026

2-Bromopyridine → (+/-)-Ethyl 4-(pyridin-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate

https://huagongshe.com/de/reaction/253115

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromopyridineHCID 7973—
EduktCesium carbonateHCID 10796—
EduktEthyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 31090—
EduktBinap, (A+-)-HCID 634876—
KatalysatorTris(dibenzylideneacetone) dipalladiumHCID 9832798—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(+/-)-Ethyl 4-(pyridin-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylateHCID 8661401555,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

In a sealable tube, tris(dibenzylideneacetone) dipalladium (0) (5.2 mg, 0.0056 mmol), (S)-BINAP (10.7 mg, 0.017 mmol), cesium carbonate (132 mg, 0.41 mmol), 2-bromopyridine (33 □L, 0.35 mmol), and ethyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate (Example 3a, 60 mg, 0.29 mmol) were dissolved in dioxane (2 mL). The reaction vessel was sealed and the suspension was heated at 100° C. for 20 h. The reaction mixture was cooled to ambient temperature, diluted with water (15 mL), and the product was extracted with dichloromethane (3×20 mL). The organic fractions were dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (15% to 25% EtOAc/hexane) afforded the title compound (46 mg, 0.16 mmol). MS m/z: 285 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872009B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-51e9447c75b04d669f08eb89eb40d763
Quellennotizuspto-grants-2011_01