Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231044Generated: October 31, 2026

Triethylamine → HCID 22724284, compound

https://huagongshe.com/reaction/2231044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22724309HCID 22724309—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22724284HCID 22724284—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(3-aminophenyl)-2-benzyl-3-oxo-3,4-dihydropyrido[2,3-b]pyrazine (339 mg), triethylamine (0.18 ml), 4-dimethylaminopyridine (5 mg) and morpholinocarbonyl chloride (0.15 ml) in 1,4-dioxane (4 ml) was stirred at 80° C. for 2 hours. Then the mixture was poured into a mixture of ethyl acetate and aqueous sodium bicarbonate. The organic phase was separated, washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel column (ethyl acetate) to give 2-benzyl-4-[3-(morpholinocarbonylamino)phenyl]-3-oxo-3,4-dihydropyrido[2,3-b]pyrazine (242 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-2e40ab02404244e48054010de5f3afb0
Source noteuspto-grants-2002_07