HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566189Generated: November 1, 2026
HCID 2166334, compound → HCID 21265538, compound
https://huagongshe.com/reaction/566189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 2166334 | HCID 2166334 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 15858722 | HCID 15858722 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21265538 | HCID 21265538 | 42.6% |
Reaction Steps
Ethyl 3-amino-4,4,4-trifluoro-2-methylcrotonate (26.0 g) was dissolved in DMF (123 ml). To this solution, a suspension of sodium methoxide in DNF (7.78 g) was added dropwise at 0° C., and the mixture was stirred at 5° C. for 30 minutes. Then, a DMF solution of ethyl N-(4-bromo-2-fluoro-phenyl)carbamate (31.44 g) was added dropwise thereto, and the mixture was stirred at 130° C. for 5 hours. After the reaction, DMF was distilled off under reduced pressure, and the residue was acidified by adding diluted hydrochloric acid thereto. This was extracted with ethyl acetate, washed with water, and then dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off, and the resulting residue was crystallized from ethyl acetate-n-hexane (1:3 v/v) to obtain the objective 3-(4-bromo-2-fluorophenyl)-5-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione (18.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174839B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-97229743c1c04a3ca01a9325971d6085 |
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| Source note | uspto-grants-2001_01 |
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