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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426273Generated: November 2, 2026

Dimethylformamide → HCID 86603473, compound

https://huagongshe.com/reaction/2426273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant4-FluorobenzylamineHCID 67326—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67148094HCID 67148094—
ProductHCID 86603473HCID 86603473—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of methyl 3-(benzoyloxy)-4-oxo-6,7-dihydro-4H-pyrido[1,2-a]pyrimidine-2-carboxylate in anhydrous DMF were added O, N-dimethylhydroxylamine hydrochloride (2.5 eq.) and DIPEA (2.2 eq.). The mixture was stirred and warmed to 65° C. for 6 h. The mixture was cooled to room temperature and the solvent was removed under high vacuum. The residue was dissolved in methanol and p-fluoro-benzylamine (2.2 eq.) and triethylamine (2 eq.) were added. The mixture was stirred at 65° C. for 16 h. After cooling to room temperature the mixture was partitioned between aq. ammonium chloride and dichloromethane. The aq. phase was again extracted with dichloromethane. The combined organic phases were then extracted with 0.1 M NaOH. The aq. phase was then acidified to pH 5 ca. with 1 M aq. HCl and extracted with dichloromethane. The organic phase was dried over sodium sulfate, filtered and concentrated to dryness. The crude product so obtained was used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968553B2
Source datasetuspto-grants-2011_06
ORD IDord-fc9aba8f4c8546c08b9c8637c467b492
Source noteuspto-grants-2011_06