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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426272Generated: November 3, 2026

Triethylamine → HCID 67148094, compound

https://huagongshe.com/reaction/2426272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 67147765HCID 67147765—
SolventDimethylformamideHCID 6228—
ProductHCID 67148094HCID 67148094—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of methyl 3-(benzoyloxy)-9-bromo-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine-2-carboxylate (obtained following Example 2, Step 1) in anhydrous DMF was added triethylamine (2 eq.). The mixture was stirred and heated to 100° C. for 3 h. After cooling to room temperature the mixture was partitioned between 0.1 M HCl and EtOAc. The aq. phase was again extracted with EtOAc and the combined org. phases were dried over sodium sulfate, filtered, concentrated to dryness under vacuum. The crude product so obtained was used in the subsequent step without further purification. An analytical sample of the title compound was obtained by crystallization from methanol. A pale yellow solid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968553B2
Source datasetuspto-grants-2011_06
ORD IDord-310dafc019c1464499564625d5fd6549
Source noteuspto-grants-2011_06