HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluorouracil → n1-(2-Maleinimidoethyloxycarbonyl)-5-fluorouracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Maleinimidoethyl chloroformate | HCID 21574820 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | n1-(2-Maleinimidoethyloxycarbonyl)-5-fluorouracil | HCID 10780306 | 61% |
Reaction Steps
500 mg (3.84 mmol) 5-fluorouracil were dissolved in 100 ml of tetrahydrofuran and diluted with 505 mg (696 μl; 4.99 mmol) of triethylamine. To this solution, 1016 mg (4.99 mmol) of 2-maleinimidoethyl chloroformate, dissolved in 100 ml of tetrahydrofuran, were added drop-wise and the set-up was stirred for 15 h at room temperature. Then, the solvent was removed under the water jet vacuum and the residue purified using column chromatography (LOBAR®-column; running medium: acetic acid/hexane 1.5/1; yield: 61%); melting point: 132° C., Rf-value: 0.64 (diol; acetic acid/hexane 2/1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06709679B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-9ac5a04f0160463b91bde775c17444d7 |
| Source note | uspto-grants-2004_03 |