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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595482Generated: October 25, 2026

4-Methylmorpholine → Ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate

https://huagongshe.com/reaction/595482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantOxalyl chlorideHCID 65578—
ReactantEthyl 2-amino-3-oxobutanoateHCID 13282896—
ReactantEthyl 6-chloro-4-(cyclobutylamino)nicotinateHCID 89689654—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoateHCID 89689546—

Reaction Steps

A stirred solution of 6-chloro-4-(isopropylamino)nicotinic acid (2) in DCM (15 mL) was cooled to 0° C., oxalyl chloride (2 equiv) was added, followed by addition of 2 drops of DMF. The reaction mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated to remove excess of oxalyl chloride. The acyl chloride, generated in-situ was dissolved in THF and added dropwise to a cool, stirred solution of ethyl 2-amino-3-oxobutanoate (1.1 equiv.) and NMM (5 equiv.) in THF. The reaction temperature was slowly brought to room temperature and stirred overnight. The reaction mixture was diluted with EtOAc and washed with water, followed by brine solution. The EtOAc layer was collected, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by column chromatography through silica gel and EtOAc:Pet. Ether as eluent to afford the title compound, ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242976B2
Source datasetuspto-grants-2016_01
ORD IDord-7a6d10f697a7416b9ad9f3f630ed45d2
Source noteuspto-grants-2016_01