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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52091Erstellt: 24. Oktober 2026

Triethylamine → N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-pyrazole-4-carboxamide

https://huagongshe.com/de/reaction/52091

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDiethyl cyanophosphonateHCID 76257—
EduktPyrazole-4-carboxylic acidHCID 3015937—
Edukt3-({4-[(Piperidin-1-yl)methyl]pyridin-2-yl}oxy)propan-1-amineHCID 14625102—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-pyrazole-4-carboxamideHCID 1996287987,1%

Reaktionsschritte

A solution of 1.0 g of 3-(4-piperidinomethyl-2-pyridyloxy)propylamine and 0.45 g of 4-pyrazolecarboxylic acid dissolved in 15 ml of dimethylformamide was stirred for 5 minutes, whilst ice-cooling, after which 734 mg of diethyl cyanophosphonate and 0.68 ml of triethylamine were added to the resulting mixture. The mixture was then stirred at room temperature for 3 hours, after which it was diluted with water, and the aqueous mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium hydrogencarbonate and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and chloroform as the eluent, to give 1.2 g (yield 85%) of the title compound as a white powder, melting at 117°-119° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616579
Quelldatensatzuspto-grants-1997_04
ORD IDord-85d42b925841424baebdad4bc27153ca
Quellennotizuspto-grants-1997_04