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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1192500Erstellt: 25. Oktober 2026

Cesium carbonate → 8-[(3S)-3-(acetylamino)pyrrolidin-1-yl]-5-chloro-N-methoxy-N-methylquinoline-7-carboxamide

https://huagongshe.com/reaction/1192500

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt(S)-(-)-3-AcetamidopyrrolidineHCID 7021471—
Edukt5-Chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonateHCID 86656172—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorBinap, (A+-)-HCID 634876—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt8-[(3S)-3-(acetylamino)pyrrolidin-1-yl]-5-chloro-N-methoxy-N-methylquinoline-7-carboxamideHCID 8665617766,1%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A stirred mixture of 5-chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonate (0.120 g, 0.301 mmol), N-[(3S)-pyrrolidin-3-yl]acetamide (0.0464 g, 0.362 mmol, Lancaster), palladium acetate (1 mg, 0.006 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (6 mg, 0.009 mmol), and cesium carbonate (0.274 g, 0.843 mmol) in tetrahydrofuran (3 mL) was heated at 65° C. overnight. The mixture was cooled, diluted with dichloromethane, and filtered. The filtrate was washed with brine, dried over sodium sulfate, and evaporated to dryness. The resultant residue was purified on silica gel, eluting with 0 to 10% MeOH in dichloromethane, to give the desired product (75 mg, 66%). LCMS calculated for C18H22ClN4O3(M+H)+: m/z=377.1; found: 377.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08680108B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-76038b1ce3674fa4b1617761a6c38be8
Quellennotizuspto-grants-2014_03