Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | HCID 20525062 | HCID 20525062 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 20525083 | HCID 20525083 | 71% |
Reaction Steps
A solution of 5-fluorouracil (2.6 g.) in N,N-dimethylacetoamide (10 ml.) was added to oily 2-tetrahydrothiophenyl isocyanate (3.1 g.). The mixture was stirred at 50° C. for 8 hours and concentrated in vacuo. The residue was treated with water (80 ml.) to give crystalline precipitates, which were collected by filtration and dried over phosphoric anhydride to give 1-[N-(2-tetrahydrothienyl)carbamoyl]-5-fluorouracil (3.68 g.); pale yellow crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04349552 |
|---|
| Source dataset | uspto-grants-1982_09 |
|---|
| ORD ID | ord-f0fb89ab656e4fa9a0187bd0ccc9d43b |
|---|
| Source note | uspto-grants-1982_09 |
|---|