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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752153Generated: November 1, 2026

Guanidine Hydrochloride → HCID 178439780, compound

https://huagongshe.com/reaction/1752153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantDiethyl allylmalonateHCID 74900—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 178439780HCID 17843978062%

Reaction Conditions

Temperature0 °C

Reaction Steps

Guanidine hydrochloride (27 g, 0.28 mol) was added to cold absolute EtOH (200 mL) and NaOEt (30% in ethanol) (200 mL), and the mixture was stirred at 0° C. for 10 min. After this time, diethyl allylmalonate (55 g, 0.28 mol) was added. The reaction mixture was then stirred at room temperature for 18 h. Acidification with 3N HCl precipitated the crude product (pH=6). The solid was collected by filtration and washed with ethanol. Recrystallization from water afforded 29 g (62%) of pure 5-allyl-2-amino-4,6-dihydroxypyrimidine (CXLIII). LCMS (ESI) m/z=168 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162992B2
Source datasetuspto-grants-2015_10
ORD IDord-380c0bd11fc34659b9affe905b214c08
Source noteuspto-grants-2015_10