HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238126Generated: October 26, 2026
Water → 4-(cyclopropylmethyl)-2-hydroxypyrido[2,3-b]pyrazin-3(4H)-one
https://huagongshe.com/reaction/238126
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | N2-(cyclopropylmethyl)pyridine-2,3-diamine | HCID 28902457 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(cyclopropylmethyl)-2-hydroxypyrido[2,3-b]pyrazin-3(4H)-one | HCID 178516909 | 33% |
Reaction Steps
To 1.6 g (9.8 mM) of N2-(cyclopropylmethyl)pyridine-2,3-diamine and 1.7 ml (9.8 mM) of diisopropylamine in 20 ml of dichloromethane were added, drop by drop, under stirring; at room temperature, 1.1 ml (9.8 mM) of ethyl chloro(oxo)acetate. The reaction mixture was stirred at room temperature for 16 h and water was added. The organic layer was separated and the aqueous layer was extracted twice with dichloromethane. The combined organic layer was washed with water, dried on anhydrous sodium sulfate and the solvent was removed under vacuum. The compound was further purified by silica gel column chromatography using dichloromethane/methanol (95/5) as eluant, which afforded after evaporation 700 mg of 4-(cyclopropylmethyl)-2-hydroxypyrido[2,3-b]pyrazin-3(4H)-one as a solid. Yield: 33%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642617B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-b8a8796af13a47fdb85efb286afa95b2 |
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| Source note | uspto-grants-2014_02 |
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