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HRID 2300040생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2300040

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참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Phenylacetyl chlorideHCID 7679—
반응물Mls002704122HCID 268729—
용매DichloromethaneHCID 6344—
생성물1,3-Dibenzyl-5-(phenylacetyl)barbituric acidHCID 995419088.8%

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온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06498164B1
출처 데이터셋uspto-grants-2002_12
ORD IDord-dabb582cc5aa4dabb93a2cbe0caa81d9
출처 메모uspto-grants-2002_12