HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31065Generated: October 26, 2026
Acetic Anhydride → 6-amino-1-isobutyl-3-methyl-2-thioxo-1H-pyrimidin-4-one
https://huagongshe.com/reaction/31065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Isobutyl-3-methylthiourea | HCID 15568243 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-amino-1-isobutyl-3-methyl-2-thioxo-1H-pyrimidin-4-one | HCID 86601056 | 29% |
Reaction Steps
A solution of cyanoacetic acid (1.52 g, 17.8 mmol) in acetic anhydride (2.45 mL, 25.9 mmol) was added to 1-isobutyl-3-methylthiourea (2.37 g, 16.2 mmol). The reaction mixture was heated to 60° C. for 1.5 h. The solvent was evaporated and the resulting red oil was redissolved in ethanol (5 mL) and 5M sodium hydroxide (1.6 mL, 8.1 mmol) was added. The reaction mixture was refluxed for 2 h. The solvent was co-evaporated with ethanol and the resulting pale brown solid was purified by flash chromatography (ethyl acetate) to yield 6-amino-1-isobutyl-3-methyl-2-thioxo-1H-pyrimidin-4-one (1.0 g, 29%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425560B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-1ed6a4e0efb34e3d84ef3149d73d0e7f |
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| Source note | uspto-grants-2008_09 |
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