Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tegafur | HCID 5386 | — |
| Reactant | Isophthaloyl chloride | HCID 7451 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hydroxy-2(1H)-pyridinone | HCID 54696004 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22150346 | HCID 22150346 | 18% |
Reaction Steps
A 1.00 g quantity of isophthaloyl chloride and 0.70 ml of triethylamine were added to a solution of 1.00 g of 5-fluoro-1-(2-tetrahydrofuranyl)uracil in 30 ml of dried dioxane. The mixture was refluxed for 2 hours. Thereto added was 1.00 ml of triethylamine and the mixture was refluxed for 2 hours. Thereto further added was 0.60 g of 4-hydroxy-2(1H)-pyridone and the mixture was refluxed for 3 hours. The solvent was distilled off and 30 ml of ethyl acetate and 30 ml of water were added to the residue. The insolubles were removed by filtration. The ethyl acetate layer was separated, dried over anhydrous sodium sulfate and concentrated. The concentrate was subjected to silica gel column chromatography to conduct gradient elution using chloroform and mixtures of methyl (up to 2%) and chloroform. The fractions corresponding to the title compound were collected and concentrated, giving 0.40 g of a powder in a yield of 18%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04864021 |
|---|
| Source dataset | uspto-grants-1989_09 |
|---|
| ORD ID | ord-cb208f76837648b9a7bfb1389e123d05 |
|---|
| Source note | uspto-grants-1989_09 |
|---|