Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Reactant | HCID 12042250 | HCID 12042250 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 10675385 | HCID 10675385 | — |
Reaction Steps
Compound 6 (2.00 g, 3.62 mmol) was dissolved in 1,2-dichloroethane (60.0 ml), and 5-fluorouracil (0.71 g, 5.46 mmol) and N,O-bis(trimethylsilyl)acetamide (5.37 ml, 21.7 mmol) were added to the solution, followed by refluxing for one hour. After the reaction mixture was allowed to cool to room temperature, trimethylsilyl trifluoromethanesulfonate (0.85 ml, 4.70 mmol) was added thereto, followed by stirring overnight at 50° C. A saturated aqueous solution of sodium hydrogencarbonate was added to the mixture, and after stirring, the organic layer was dried over anhydrous magnesium sulfate. The residue was purified by means of silica gel column chromatography (silica gel 300 ml, eluent; n-hexane:ethyl acetate=3:1), to thereby yield a colorless viscous compound (Compound 31; 0.80 g, 1.28 mmol, 35.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06291670B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-03f0102b7a0f47cc934b819f6a4f85c8 |
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| Source note | uspto-grants-2001_09 |
|---|