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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1461616Erstellt: 24. Oktober 2026

Pyridine → 3,5-Dioxohexanoic acid

https://huagongshe.com/de/reaction/1461616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktAcetic AnhydrideHCID 7918—
EduktDimethylacetamideHCID 31374—
Edukt3-[(2-Hydroxyethyl)amino]propane-1,2-diolHCID 15034945—
LösungsmittelSodium CarbonateHCID 10340—
Produkt3,5-Dioxohexanoic acidHCID 5459844—

Reaktionsschritte

As in Example 12, the title compound is prepared stepwise by first reacting 5-amino-2,4,6-triiodo-3-N-methylaminocarbonylbenzoyl chloride with 3-(N-2-hydroxyethyl)amino-1, 2-propanediol dissolved in DMAc in the presence of sodium carbonate. The product, 5-amino[N-(2,3,-dihydroxypropyl)-N-(2-hydroxyethyl]-2,4,6-triiodo-3-N-methylaminocarbonylbenzamide, is reacted with acetic anhydride in the presence of pyridine to produce the triacetate, [N-(2-acetoxyethyl)-N-(2,3-diacetoxypropyl)]-5-amino-,4,6-triiodo -3-N-methylaminocarbonylbenzamide. This compound is then reacted with 2,4-dibromobutryl bromide, prepared as in Example 12, Step B, and the product is then cyclized, hydrolyzed, and purified as in Example 12, Steps D and E to produce the final product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05075502
Quelldatensatzuspto-grants-1991_12
ORD IDord-fc367aa39780419a8b3544359115cef5
Quellennotizuspto-grants-1991_12