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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1981361Erstellt: 26. Oktober 2026

4-Nitrophenyl 1-oxo-1lambda~5~-pyridine-3-carboxylate → N-[3-[3-(3-methylpiperidinomethyl)phenoxy]propyl]-3-pyridinecarboxamide 1-oxide

https://huagongshe.com/reaction/1981361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrophenyl 1-oxo-1lambda~5~-pyridine-3-carboxylateHCID 13364676—
Edukt3-{3-[(3-Methylpiperidin-1-yl)methyl]phenoxy}propan-1-amineHCID 14026188—
LösungsmittelMethanolHCID 887—
ProduktN-[3-[3-(3-methylpiperidinomethyl)phenoxy]propyl]-3-pyridinecarboxamide 1-oxideHCID 6917813—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To the active ester thus obtained there is added a solution of 3.8 g of 3-[3-(3-methylpiperidinomethyl)phenoxy]propylamine in 70 ml of methanol and the mixture is stirred 3 hours at 50° C. The solvent is evaporated, the residue is taken up with 30 ml of N hydrochloric acid and the acid solution is washed 3 times with 20 ml of ethyl acetate. The pH is adjusted to 7.8, then the solution is salted out with sodium chloride and extracted 6 times with 30 ml of ethyl acetate. The organic extracts are collected and dried over anhydrous sodium sulfate and the solvent in evaporated to dryness. The product is purified by chromatography on silica as described in Example 7. Thus, the N-[3-[3-(3-methylpiperidinomethyl)phenoxy]propyl]-3-pyridinecarboxamide 1-oxide is obtained, identical to the product of Example 8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04514408
Quelldatensatzuspto-grants-1985_04
ORD IDord-29b42e2237774cae9ea78342356694ea
Quellennotizuspto-grants-1985_04