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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402989Generated: October 30, 2026

Acetone → Tert-butyl 4-(2-oxo-1,2-dihydropyrido[2,3-b]pyrazin-8-yloxy)phenylcarbamate

https://huagongshe.com/reaction/1402989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantEthyl oxoacetateHCID 70211—
ReactantTert-butyl 4-(2,3-diaminopyridin-4-yloxy)phenylcarbamateHCID 42625416—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(2-oxo-1,2-dihydropyrido[2,3-b]pyrazin-8-yloxy)phenylcarbamateHCID 4690075045%

Reaction Steps

tert-butyl 4-(2,3-diaminopyridin-4-yloxy)phenylcarbamate (0.86 g, 2.71 mmol) was dissolved in 15 ml of dry ethanol; 0.8 ml (4 mmol) of a 50% ethyl glyoxalate solution in toluene were added and the solution was stirred overnight at room temperature under Argon atmosphere. The solvent was partially evaporated, and tert-butyl 4-(2-oxo-1,2-dihydropyrido[2,3-b]pyrazin-8-yloxy)phenylcarbamate (0.430 g, 45% yield) is precipitated by addition of acetone (10 ml) and filtered off.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912191B2
Source datasetuspto-grants-2014_12
ORD IDord-a0dd637c081840218fd9c0c3720d1d7a
Source noteuspto-grants-2014_12