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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395790Erstellt: 24. Oktober 2026

Pyridine → N-(4-methoxyphenyl)-2-[[1-(4-pyridyl)piperidin-4-ylcarbonyl]amino]benzamide

https://huagongshe.com/de/reaction/395790

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktThionyl ChlorideHCID 24386—
Edukt2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
Edukt1-(Pyridin-4-yl)piperidine-4-carboxylic acidHCID 1268289—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(4-methoxyphenyl)-2-[[1-(4-pyridyl)piperidin-4-ylcarbonyl]amino]benzamideHCID 1817454530,2%

Reaktionsschritte

To a stirred suspension of N-(4-pyridyl)isonipecotic acid (0.2 g, 1 mmol) in dichloromethane (70 mL) was added thionyl chloride (0.11 mL, 1.5 mmol). After stirring overnight, the solvent was removed in vacuo and the residue was dissolved in dichloromethane (10 mL) and added to a stirred solution of 2-amino-N-(4-methoxyphenyl)benzamide (0.186 g, 0.77 mmol) and pyridine (0.19 g, 0.85 mmol) in dichloromethane (25 mL). After stirring for 72 h, the solution was transferred to a separatory funnel and washed with water, saturated aqueous sodium bicarbonate solution, and saturated aqueous sodium chloride solution. The organic phase was dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was suspended in a mixture of diethyl ether and hexanes, sonicated, and filtered. The resulting solid was washed with diethyl ether and dried in vacuo to give 0.10 g (30%) of the title compound as a pale tan solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605626B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-7ac8badbfd9c4996afebd2dc23dd7fda
Quellennotizuspto-grants-2003_08