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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-oxo-3-(pyrimidin-4-yl)propanoate | HCID 11961458 | — |
| Reactant | 2,3,6,7-Tetrahydro-[1,4]oxazepin-5-ylamine monohydrochloride | HCID 22617759 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Pyrimidin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-one | HCID 66846036 | 53.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507470B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-1594454a0bf24065bf2d3faa456bde46 |
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| Source note | uspto-grants-2013_08 |
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