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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340201Erstellt: 25. Oktober 2026

Potassium Carbonate → HCID 58213743, Verbindung

https://huagongshe.com/reaction/340201

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt(2-BOC-aminophenyl)boronic acidHCID 2773226—
Edukt3-Bromo-6-methoxypyridine-2-carbonitrileHCID 53485627—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 58213743HCID 58213743—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A solution of 2-(tert-butoxycarbonylamino)phenylboronic acid (1.0 eq.) and 3-bromo-6-methoxypicolinonitrile (from step 1) (1.0 eq.) in toluene (0.44 M) was mixed with tetrakis(triphenyl-phosphine)palladium (5 mol %) and 2N aqueous potassium carbonate solution (2.0 eq.). The reaction was heated to 100° C. and stirred overnight. After cooling to ambient temperature, the reaction content was diluted with 2% methanol in dichloromethane and water. The two phases were separated, and the aqueous layer was extracted twice with 2% methanol in dichloromethane. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-50% ethyl acetate in hexane to give 3-methoxybenzo[f][1,7]naphthyridin-5-amine as a yellow solid. 1H NMR (acetone d-6): δ 8.91 (d, 1H), 8.34 (d, 1H), 7.63 (d, 1H), 7.51-7.53 (dd, 1H), 7.27-7.33 (m, 2H), 6.65 (br, 2H), 4.11 (s, 3H). LRMS [M+H]=226.1

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895577B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-fbb593076b3e458499a850d113c39646
Quellennotizuspto-grants-2014_11