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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2300041Erstellt: 26. Oktober 2026

Pyridine → 1,3-Dibenzyl-5-(2-thienylacetyl)barbituric acid

https://huagongshe.com/reaction/2300041

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDiethyl EtherHCID 3283—
Edukt2-Thiopheneacetyl chlorideHCID 162362—
EduktMls002704122HCID 268729—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,3-Dibenzyl-5-(2-thienylacetyl)barbituric acidHCID 988903570,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1,3-dibenzylbarbituric acid 154 mg (0.500 mmol) in dry dichloromethane 2.0 mL under a nitrogen atmosphere, added was pyridine 1.0 mL (12 mmol) and stirred at 0° C. Added was 2-thienylacetyl chloride 80 mg (0.50 mmol, 1.00 equivalent) in dichloromethane 1.0 mL to the solution slowly during a period of 20 minutes, then stirred at room temperature for 3 hours. Added was ether 50 mL and washed the organic layer with 2 M hydrochloric acid and saturated brine, and dried over sodium sulfate. Purified was the crude product 216 mg after removal of the solvent under the reduced pressure, by column chromatography (silica gel, eluted with dichloromethane). It obtained 1,3-dibenzyl-5-(2-thienylacetyl)barbituric acid 153 mg as yellow viscous oil (56.9% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06498164B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-3c1f3b0149b84b2bb77617a4f1ff0a3c
Quellennotizuspto-grants-2002_12