Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Hexyl isocyanate | HCID 75659 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Carmofur | HCID 2577 | 75% |
Reaction Steps
13.0g (0.10 mole) of 5-fluorouracil was suspended in 60 ml of dimethyl acetamide, then 14.0g (0.11 mole) of n-hexyl isocyanate was added thereto at room temperature and stirred at 50° C for 8 hours. After the reaction mixture was concentrated under reduced pressure, the residue was poured into 400 ml of water and resultant precipitate was filtered off. The precipitate was washed and dried and 19.3g (75.0% yield) of 5-fluoro-1-(n-hexylcarbamoyl)uracil was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04071519 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-32199e7ae65a4ff194f679bb9b1f5b97 |
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| Source note | uspto-grants-1978_01 |
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