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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547378Generated: October 30, 2026

Triethylamine → HCID 54730629, compound

https://huagongshe.com/reaction/547378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-FluorobenzylamineHCID 67326—
ReactantHCID 67198751HCID 67198751—
SolventMethanolHCID 887—
ProductHCID 54730629HCID 54730629—

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 3-[(pivaloyl)oxy]-4-oxo-4H-pyrido[1,2-a]pyrimidine-2-carboxylate was dissolved in methanol. p-Fluorobenzylamine (2 eqs.) was added and the reaction was stirred and heated to 60° C. for 2 hours. A precipitate had formed and further methanol and 1 eq. of triethylamine were added. After 2 more hours at 60° C. the reaction mixture was partitioned between EtOAc and 1 M HCl. The organic phase was extracted with 0.1 M aqueous NaOH. The aqueous phase was separated and acidified with 1 M HCl. The aqueous phase was extracted with EtOAc and the organic phase was dried over Na2SO4, filtered and concentrated to dryness. The title compound was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939537B2
Source datasetuspto-grants-2011_05
ORD IDord-1f3036b512404e53830b69701d430c8f
Source noteuspto-grants-2011_05