Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1981363Erstellt: 26. Oktober 2026

Oxiniacic Acid → N-[3-[3-(3-methylpiperidinomethyl)phenoxy]propyl]-3-pyridinecarboxamide 1-oxide

https://huagongshe.com/reaction/1981363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxiniacic AcidHCID 16976—
Edukt2-DimethylaminopyridineHCID 21885—
Edukt3-{3-[(3-Methylpiperidin-1-yl)methyl]phenoxy}propan-1-amineHCID 14026188—
EduktHCID 178486078HCID 178486078—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-[3-[3-(3-methylpiperidinomethyl)phenoxy]propyl]-3-pyridinecarboxamide 1-oxideHCID 6917813—

Reaktionsschritte

To a suspension of 2.8 g of nicotinic acid 1-oxide, 2.5 g of dimethylaminopyridine, 8.8 g of benzotriazolyloxy-tris-(dimethylamino)phosphonium hexafluorophosphate in 40 ml of acetonitrile, 5 g of 3-[3-(3-methylpiperidinomethyl)phenoxy]propylamine dissolved in 10 ml of acetonitrile are added at 20° C. under stirring. A rising of the temperature up to 30° C. is observed and a solution is obtained which is then stirred 2 hours at room temperature. The mixture is concentrated under reduced pressure, the residue is treated with 20 ml of concentrated sodium hydroxide and extracted 4 times with 40 ml of ethyl acetate. After evaporation of the organic extracts, the residue 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-0569039e773c45058c59c1bbc81b622d
Quellennotizuspto-grants-1985_04