HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574125Generated: October 27, 2026
Acetic Anhydride → 6-Amino-1,3-diethyl-2,4(1H,3H)-pyrimidinedione
https://huagongshe.com/reaction/574125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | sym-Diethylurea | HCID 12194 | — |
| Product | 6-Amino-1,3-diethyl-2,4(1H,3H)-pyrimidinedione | HCID 603026 | — |
Reaction Steps
12.69 grams (0.14 mol) of diethylurea and 11.90 grams (0.14 mol) of cyanoacetic acid were heated in acetic anhydride at 60° C. for 3 hours, under dry atmosphere. Thereafter, the acetic anhydride and remaining cyanoacetic acid were evaporated, 5% sodium hydroxide was added and the mixture was stirred and cooled. 20 grams of 6-amino-1,3-diethyluracil were obtained as a precipitate. 11.8 grams of sodium nitrite in 70 ml water were then added while cooling and stirring and the solution was then acidified by adding 70 ml acetic acid. The mixture was stirred at room temperature for additional 2.5 hours. The resulting precipitate was filtered, washed with water, ethanol and finally ether so afford 10.1 grams of 6-amino-1,3-diethyl-5-nitrosouracil, as a violet product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034872B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-2c8a55c244184394a7894919c1f4cab0 |
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| Source note | uspto-grants-2015_05 |
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