HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075143Generated: November 2, 2026
5-Chloro-2(1H)-pyrimidinone → HCID 22823685, compound
https://huagongshe.com/reaction/1075143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Chloro-2(1H)-pyrimidinone | HCID 108578 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 12903138 | HCID 12903138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22823685 | HCID 22823685 | 50% |
Reaction Steps
2-Desoxy-2-acetylamino-3,4,6-tri-O-actyl-D-glucopyranosylchloride (0.01 mol) and the potassium salt of 5-chloropyrimid-2-one (0.008 mol) were heated together in dimethylformamide (60 ml) with stirring at 80° C. for 24 hours. The solvent was then evaporated at reduced pressure (1 mm Hg) and the residue was extracted with chloroform (120 ml). The chloroform solution was washed with aqueous 1 N NaOH (2×3 ml) and water (3 ml) before drying (Mg SO4). Evaporation left the title compound which was further purified by trituration with ether and recrystallization from a small volume of methanol; yield 50%, m.p. 165°-167° C. when the sample is heated rapidly. (Found: C, 47.00; H, 4.82. Calc. for C18H22ClN3O9: : C, 47.02; H, 4.82)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04395406 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-909a5763061042dbbd27d547e95ba664 |
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| Source note | uspto-grants-1983_07 |
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