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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913083Generated: October 26, 2026

Water → 4-(cyclopropylmethyl)-2-hydroxypyrido[2,3-b]pyrazin-3(4H)-one

https://huagongshe.com/reaction/1913083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylamineHCID 7912—
ReactantEthoxalyl chlorideHCID 20884—
ReactantN2-(cyclopropylmethyl)pyridine-2,3-diamineHCID 28902457—
SolventDichloromethaneHCID 6344—
Product4-(cyclopropylmethyl)-2-hydroxypyrido[2,3-b]pyrazin-3(4H)-oneHCID 17851690933%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609689B2
Source datasetuspto-grants-2013_12
ORD IDord-e721f19ccdcb42e98cf089e390321ca7
Source noteuspto-grants-2013_12