HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703549Generated: October 28, 2026
Isophthaloyl chloride → HCID 178476350, compound
https://huagongshe.com/reaction/703549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isophthaloyl chloride | HCID 7451 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridine | HCID 13687484 | — |
| Reactant | 4-Hydroxy-2(1H)-pyridinone | HCID 54696004 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178476350 | HCID 178476350 | 30.1% |
Reaction Steps
To a solution of 3.00 g of 5'-O-acetyl-3'--O--benzyl- 2'-deoxy-5-fluorouridine in 100 ml of dry dioxane were added 2.40 g of isophthaloyl chloride and 8.5 ml of triethylamine, and the mixture was refluxed for 2 hours. Then, to the reaction mixture were added a suspension of 1.77 g of 4-hydroxy-2(1H)-pyridone and 9.60 ml of triethylamine in 100 ml of dry dioxane, and the mixture was refluxed for 2 hours. The insolubles were removed by filtration and the filtrate was concentrated. The residue was dissolved in 100 ml of ethyl acetate, and the solution was washed twice with 30 ml of saturated aqueous solution of sodium chloride. The ethyl acetate layer was dried on anhydrous sodium, sulfate and concentrated. The residue was placed on a silica gel column to conduct a gradient elution using chloroform and mixtures of methanol (up to 2%) and chloroform. The fractions corresponding to the title compound were collected and concentrated to dryness, giving 1.48 g of the title compound as a powder in a yield of 30%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983609 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-4b1fbd5698854f948801056f0d61c61f |
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| Source note | uspto-grants-1991_01 |
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