HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485314Generated: October 30, 2026
Pyridine → propan-2-yl 5-fluoro-4-[(Z)-furan-2-ylmethylideneamino]oxy-2,6-dioxo-1,3-diazinane-5-carboxylate
https://huagongshe.com/reaction/485314
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 5354160 | HCID 5354160 | — |
| Reactant | HCID 12901281 | HCID 12901281 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | propan-2-yl 5-fluoro-4-[(Z)-furan-2-ylmethylideneamino]oxy-2,6-dioxo-1,3-diazinane-5-carboxylate | HCID 88687967 | 32.8% |
Reaction Steps
In 50 ml of acetone was dissolved 20.0 g (85.4 mmol) of isopropyl 5-fluoro-6-hydroxy-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5-carboxylate, and 8.78 g (111.0 mmol) of pyridine and 8.65 g (93.9 mmol) of acetic anhydride were added to the solution, followed by stirring under ice-cooling for 3 hours and subsequently at room temperature for 16 hours. The solvent was disttiled off under reduced pressure, and the acetylated compound, which precipitates after the addition of water, was recovered by filtration, washed with water and dried. One-half its amount and 5.70 g (51.2 mmol) of (Z)-furfuraldoxime were dissolved in 30 ml of pyridineacetone (pyridine:acetone=2.1), and the solution was stirred at 60° C. for 15 hours. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography with hexane-ethyl acetate changing gradually the mixing ratio from (9:1) to (1:2) to yield 5.5 g of 5-fluoro-6-[(Z)-furfurylideneaminooxy]-5-isopropyloxycarbonyl-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine. m.p. 131°-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536504 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-d49433a840db4c06be021b2d2711b321 |
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| Source note | uspto-grants-1985_08 |
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