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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 2-Thiopheneacetyl chloride | HCID 162362 | — |
| Edukt | Mls002704122 | HCID 268729 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1,3-Dibenzyl-5-(2-thienylacetyl)barbituric acid | HCID 9889035 | 70,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06498164B1 |
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| Quelldatensatz | uspto-grants-2002_12 |
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| ORD ID | ord-3c1f3b0149b84b2bb77617a4f1ff0a3c |
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| Quellennotiz | uspto-grants-2002_12 |
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