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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300040Generated: October 26, 2026

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

https://huagongshe.com/reaction/2300040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantMls002704122HCID 268729—
SolventDichloromethaneHCID 6344—
Product1,3-Dibenzyl-5-(phenylacetyl)barbituric acidHCID 995419088.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,3-dibenzyl barbituric acid 192 mg (0.623 mmol) in dry dichloromethane 2.0 mL under nitrogen atmosphere, added was pyridine 1.0 mL (12 mmol) and stirred at 0° C. Added was phenylacetyl chloride 96 mg (0.623 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 dichloromethane 40 mL and washed the organic layer with 2 M hydrochloric acid and saturated brine, and dried over sodium sulfate. Purified was the crude product 273 mg, after removal of the solvent under the reduced pressure, by column chromatography (silica gel, eluted with dichloromethane). It obtained 1,3-dibenzyl-5-(phenylacetyl)barbituric acid 236 mg as colorless viscous oil at first (88.7% yield) and it gradually turned white plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498164B1
Source datasetuspto-grants-2002_12
ORD IDord-dabb582cc5aa4dabb93a2cbe0caa81d9
Source noteuspto-grants-2002_12