HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluorouracil → Tegafur
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tegafur | HCID 5386 | — |
Reaction Steps
In 15 ml of dimethylformamide were dissolved 1.3 g of 5-fluorouracil and 0.41 g of triethylamine hydrochloride. To this solution were added 3 ml of 2,3-dihydrofuran and the mixture was reacted in an autoclave for 16 hours at 150° C. After the reaction, dimethylformamide was removed from the reaction liquid by distillation and the residue was treated in the same manner as described in Example 7 to obtain 0.8 g of 1-(2-tetrahydrofuryl)-5-fluorouracil. From the chloroform insoluble matter 0.6 g of the starting 5-fluorouracil was recovered. The yield of the end product was 74% based on the consumed 5-fluorouracil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256885 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-b1afd9df20d24dd3b2dad69e2b37af88 |
| Source note | uspto-grants-1981_03 |