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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 626506Erstellt: 25. Oktober 2026

Water → 1-methyl-N-(4-((6-nitropyridin-3-yl)oxy)pyridin-2-yl)piperidine-4-carboxamide

https://huagongshe.com/reaction/626506

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCesium carbonateHCID 10796—
Edukt1-Methylpiperidine-4-carboxamideHCID 339011—
Edukt2-Chloro-4-((6-nitropyridin-3-yl)oxy)pyridineHCID 59322779—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-methyl-N-(4-((6-nitropyridin-3-yl)oxy)pyridin-2-yl)piperidine-4-carboxamideHCID 9041085356,3%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of Example A1 (0.25 g, 0.994 mmol), Cs2CO3 (0.486 g, 1.490 mmol), 1-methylpiperidine-4-carboxamide (0.155 g, 1.093 mmol), and X-phos (0.024 g, 0.050 mmol) in dioxane (5 mL) was sparged with Ar, treated with Pd2(dba)3 (0.045 g, 0.050 mmol) and heated at 90° C. overnight. Additional X-phos (17 mg) and Pd2(dba)3 (30 mg) were added and the mixture heated at 90° C. for 7 h. The mixture was cooled to RT, treated with water and extracted with EtOAc (3×). The combined organics were dried over Na2SO4, concentrated to dryness and purified via silica gel chromatography (MeOH/DCM) to afford 1-methyl-N-(4-((6-nitropyridin-3-yl)oxy)pyridin-2-yl)piperidine-4-carboxamide (200 mg, 56%). MS (ESI) m/z: 358.2 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09309224B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-0845a84a8fe1403d90b87b4f790ca1ea
Quellennotizuspto-grants-2016_04