HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isophthaloyl chloride → 5'-O-acetyl-3-[3-(4-benzoyloxy-5-chloro-2-pyridyloxycarbonyl)benzoyl]-3'-O-benzyl-2'-deoxy-5-fluorouridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isophthaloyl chloride | HCID 7451 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridine | HCID 13687484 | — |
| Reactant | 5-Chloro-2-oxo-1,2-dihydropyridin-4-yl benzoate | HCID 14049646 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5'-O-acetyl-3-[3-(4-benzoyloxy-5-chloro-2-pyridyloxycarbonyl)benzoyl]-3'-O-benzyl-2'-deoxy-5-fluorouridine | HCID 18634814 | 37.4% |
Reaction Steps
To a solution of 0.60 g of 5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridine in 30 ml of dry dioxane were added 0.42 g of isophthaloyl chloride and 1.11 ml of triethylamine, and the mixture was refluxed for 2 hours. Then 0.60 g of 4-benzoyloxy-5-chloro-2(1H)-pyridone and 1.11 ml of triethyl amine were added and the resulting mixture was refluxed for 1 hour. The precipitate thus formed was filtered off, and the filtrate was concentrated. The residue was placed on a silica gel column and eluted with 40% ethyl acetate-benzene, giving 0.45 g of the title compound in a yield of 37%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983609 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-ba9781ca37d84e488918675ad90467f5 |
| Source note | uspto-grants-1991_01 |