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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349469Generated: October 31, 2026

Ethanol → HCID 58859156, compound

https://huagongshe.com/reaction/1349469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantHCID 58859128HCID 58859128—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58859156HCID 58859156—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-benzyloxy-5-(1-hydroxy-2,2-dimethylpropyl)-4-oxo-4H-pyran-2-carboxylic acid 3-chlorobenzylamide (0.22 g) in tetrahydrofuran (1.5 ml)-ethanol (1.5 ml) was added aminoacetaldehyde dimethyl acetal (0.16 ml) and the mixture was stirred at 60° C. for 24 hr. The solvent was evaporated and purified by silica gel column chromatography (ethyl acetate:hexane=1:1-ethyl acetate) to give 3-benzyloxy-1-(2,2-dimethoxyethyl)-5-(1-hydroxy-2,2-dimethylpropyl)-4-oxo-1,4-dihydropyridine-2-carboxylic acid 3-chlorobenzylamide (198 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211572B2
Source datasetuspto-grants-2007_05
ORD IDord-9da79416d9ee41bbb5de4a6e6121eeaf
Source noteuspto-grants-2007_05