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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890237Generated: October 31, 2026

Potassium Carbonate → Pyrimidin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-one

https://huagongshe.com/reaction/1890237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-oxo-3-(pyrimidin-4-yl)propanoateHCID 11961458—
Reactant2,3,6,7-Tetrahydro-[1,4]oxazepin-5-ylamine monohydrochlorideHCID 22617759—
SolventEthanolHCID 702—
ProductPyrimidin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-oneHCID 6684603653.5%

Reaction Steps

To a suspension of 25.00 g (165.99 mmol) of 2,3,6,7-tetrahydro-[1,4]oxazepin-5-ylamine monohydrochloride (synthesis as described in WO97/16430 and Bioorganic & Medicinal Chemistry Letters (2004), 14(23), 5907-5911) in 550 mL of ethanol was added 25.23 g (182.59 mmol) of potassium carbonate. The reaction mixture was stirred at room temperature for 10 min, 35.45 g (182.59 mmol) of ethyl 3-(4-pyrimidinyl)-3-oxopropionate was added and the resulting mixture was stirred under reflux for 4 hours. The cooled solution was evaporated to remove solvent. The mixture was dissolved with water and diethyl ether. After stirring, the resulting solid was filtered, washed with water and diethyl ether to afford 21.7 g (53%) of the desired compound as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507470B2
Source datasetuspto-grants-2013_08
ORD IDord-1594454a0bf24065bf2d3faa456bde46
Source noteuspto-grants-2013_08