Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | 3-(2-Thienyl)propyl isocyanate | HCID 20525111 | — |
| Product | HCID 20525101 | HCID 20525101 | — |
Reaction Steps
5-Fluorouracil (3.30 g.) was added to the solution of 3-(2-thienyl)propyl isocyanate and stirred at 100° C. for 2 hours. The resultant mixture was evaporated to dryness under reduced pressure. The residue was dissolved in ethyl acetate, washed with water, dried over magnesium sulfate, filtered and evaporated under reduced pressure. The residue was recrystallized from ethanol to give colorless plate 1-[N-[3-(2-thienyl)propyl]carbamoyl]-5-fluorouracil (2.3 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04349552 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-ceed66503e8f4ef78c02845b041bda67 |
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| Source note | uspto-grants-1982_09 |
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