Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluridine | HCID 6256 | — |
| Reactant | HCID 19792576 | HCID 19792576 | — |
| Reactant | HCID 54403406 | HCID 54403406 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 14722799 | HCID 14722799 | — |
| Product | HCID 14722801 | HCID 14722801 | — |
Reaction Steps
1.00 Gram of 2'-deoxy-5-trifluoromethyluridine was dissolved in 15 ml of 1,4-dioxane. Thereto were added 2.50 g of bis-(α,α-dimethylbenzyloxy)methane and 38 mg of toluenesulfonic acid anhydride. They were heated to 60° C. and stirred for 3.5 hours. The reaction mixture was subjected to evaporation. The residue was subjected to silica gel column chromatography wherein a developing solvent of chloroform-methanol (20:1) was first used for preliminary separation and then a developing solvent of benzene-acetone (10:1) was used, to obtain 0.40 g (yield: 29.2%) of hygroscopic and amorphous 2'-deoxy-5'-O-(α,α-dimethylbenzyl)-5-trifluoromethyluridine (compound 22) and 0.28 g (yield: 20.4%) of hygroscopic and amorphous 2'-deoxy-3'-O-(α,α-dimethylbenzyl)-5-trifluoromethyluridine (compound 23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886877 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-d55036830e7d4fad91b850966dfbf35f |
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| Source note | uspto-grants-1989_12 |
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