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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1799202Erstellt: 26. Oktober 2026

Potassium Carbonate → Methyl 2-{[5-((3R)-5-Oxopyrrolidin-3-yl)-2-chlorophenyl]amino}benzoate

https://huagongshe.com/reaction/1799202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktMethyl 2-bromobenzoateHCID 11894—
Edukt2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Edukt(4R)-4-(3-amino-4-chlorophenyl)pyrrolidin-2-oneHCID 66724932—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktMethyl 2-{[5-((3R)-5-Oxopyrrolidin-3-yl)-2-chlorophenyl]amino}benzoateHCID 66725153—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixture of (4R)-4-(3-amino-4-chlorophenyl)pyrrolidin-2-one (0.18 g, 0.86 mmol), methyl 2-bromobenzoate (0.37 g, 1.72 mmol), palladium acetate (0.038 g, 0.172 mmol), and Buchwald's reagent (2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl) (0.122 g, 0.256 mmol) was added dioxane (2 mL). The mixture was degassed by alternatively applying a vacuum and flushing with nitrogen for a few cycles. After 15 minutes, potassium carbonate (0.237 g, 1.72 mmol) was added. The mixture was stirred overnight at 100° C., and then cooled to room temperature and filtered through Celite. The filtrate was washed with an aqueous HCl solution and extracted with ethyl acetate (3 times). The ethyl acetate layers were then washed with brine and concentrated to give the title compound (13a) as a brown residue which was used directly in the next step. MS (ESI) m/z 345 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08344028B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-b990302f28e646dc9060359215fe48a8
Quellennotizuspto-grants-2013_01