HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719552Generated: October 30, 2026
Sodium → 2-Nitroamino-5-[1-(2-dimethylaminoethyl)-2-oxopyridin-4-ylmethyl]pyrimidin-4-one
https://huagongshe.com/reaction/1719552
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium | HCID 5360545 | — |
| Reactant | ethyl alpha-formyl-beta-(N-(2-dimethylaminoethyl)-2-oxo-4-pyridyl]propionate | HCID 20267140 | — |
| Reactant | Nitroguanidine | HCID 86287517 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Nitroamino-5-[1-(2-dimethylaminoethyl)-2-oxopyridin-4-ylmethyl]pyrimidin-4-one | HCID 70354145 | 39.6% |
Reaction Steps
To a stirred solution of sodium (2.94 g) in methanol (65 ml) was added nitroguanidine (11.81 g, containing 25% w/w water) and methanol (20 ml). The mixture was stirred at reflux for 60 minutes, and then a solution of ethyl α-formyl-β-(N-(2-dimethylaminoethyl)-2-oxo-4-pyridyl]propionate (25.05 g) in methanol (75 ml) was added dropwise over 90 minutes. The reaction mixture was stirred under reflux for a further 21 hours. The reaction mixture was evaporated under reduced pressure, dissolved in water (150 ml) and extracted with chloroform (3×35 ml). The combined chloroform extracts were washed with water (2×10 ml). The combined aqueous layer and aqueous washings were taken to pH 4 with glacial acetic acid. The solvent was then evaporated under reduced pressure and a solid by-product crystallised from ethanol. The mother liquors were evaporated and another crystallisation from ethanol gave a further solid by-product. The mother liquor was evaporated under reduced pressure to afford 2-nitroamino-5-[1-(2-dimethylaminoethyl)-2-oxopyridin-4-ylmethyl]pyrimidin-4-one (11.26 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04540699 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-c940acfbcc654b08a870593d41e1654c |
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| Source note | uspto-grants-1985_09 |
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