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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20650Erstellt: 23. Oktober 2026

Triethylamine → methyl 5-chloro-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)nicotinate

https://huagongshe.com/de/reaction/20650

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
Edukt4-(3-bromo-5-chloropyridin-4-ylamino)-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-oneHCID 24849432—
EduktHCID 178418416HCID 178418416—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
Produktmethyl 5-chloro-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)nicotinateHCID 86618135—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Carbon monoxide was bubbled through a mixture of 4-(3-bromo-5-chloropyridin-4-ylamino)-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-one (0.240 g, 0.514 mmol, Example 11), Pd(OAc)2 (11 mg, 0.051 mmol), DPPP (21 mg, 0.051 mmol), triethylamine (0.22 mL, 1.5 mmol), methanol (1 mL), and anhydrous DMF (4 mL). The reaction was heated at 80° C. for 2 d under an atmosphere of CO and then allowed to cool to rt. The mixture was filtered though Celite, washed with EtOAc, and concentrated to give methyl 5-chloro-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)nicotinate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745646B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-fdf8967d91d349038d721fcbf25a7dc0
Quellennotizuspto-grants-2010_06