HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluorouracil → 1(2H)-Pyrimidinecarboxamide, N-butyl-5-fluoro-3,4-dihydro-2,4-dioxo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1(2H)-Pyrimidinecarboxamide, N-butyl-5-fluoro-3,4-dihydro-2,4-dioxo- | HCID 116542 | 72.4% |
Reaction Steps
13.0g (0.10 mole) of 5-fluorouracil was dissolved in 70 ml of dimethyl formamide, then 11.9g (0.12 mole) of n-butyl isocyanate was added thereto at room temperature and stirred at the same temperature for 24 hours. The reaction mixture was concentrated to 40ml by removing dimethyl formamide and excess n-butyl isocyanate under reduced pressure. The residue was poured into 300ml of water and resultant precipitate was filtered off. The precipitate was washed and dried and 16.6g (72.3% yield) of 1-(n-butylcarbamoyl)-5-fluorouracil was obtained
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04071519 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-d9b1029cb8e94d3ca81e29df96f4a0d7 |
| Source note | uspto-grants-1978_01 |