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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930679Generated: November 1, 2026

Water → 6-acetyl-2-[4-(1,3-oxazol-5-yl)anilino]-1,5,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-one

https://huagongshe.com/reaction/1930679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ethoxideHCID 2723922—
ReactantMethyl 1-acetyl-4-oxopiperidine-3-carboxylateHCID 14143329—
Reactant1-(4-(Oxazol-5-yl)phenyl)guanidineHCID 178512471—
SolventEthanolHCID 702—
Product6-acetyl-2-[4-(1,3-oxazol-5-yl)anilino]-1,5,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-oneHCID 17847376540.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-(4-(Oxazol-5-yl)phenyl)guanidine (2 g, 9.89 mmol, example 1e), methyl 1-acetyl-4-oxopiperidine-3-carboxylate (1.970 g, 9.89 mmol) and sodium ethoxide (0.673 g, 9.89 mmol) in ethanol were charged in a thick wall glass which was sealed and heated at 100° C. under microwave irradiation. The reaction mixture was allowed to reach room temperature and water was added until a solid was obtained. The solid was filtered and dried in a vacuum oven at 40° C. overnight yielding 1-(4-hydroxy-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)ethanone (1.400 g, 40.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188101B2
Source datasetuspto-grants-2012_05
ORD IDord-07f8250ed1b64cd99bade80f095080a9
Source noteuspto-grants-2012_05