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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935147Generated: October 30, 2026

4-Methylmorpholine → N-{3-Cyano-4-[(3,4-difluorophenyl)amino]-6-quinolinyl}-2-butynamide

https://huagongshe.com/reaction/1935147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-Butynoic acidHCID 68535—
Reactant6-Amino-4-[(3,4-difluorophenyl)amino]-3-quinolinecarbonitrileHCID 22466570—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-{3-Cyano-4-[(3,4-difluorophenyl)amino]-6-quinolinyl}-2-butynamideHCID 2246660760.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolved 425 mg (5.06 mmol) 2-butynoic acid in 40 ml THF and chilled to 0° C. under N2. Added 556 μl (5.06 mmol) N-methylmorpholine and 658 μl (5.06 mmol) isobutyl chloroformate and stirred for 10 minutes. Added dropwise a solution of 1.00 g (3.37 mmol) 6-amino-4-[(3,4-difluorophenyl)amino]-3-quinolinecarbonitrile in 2.0 ml hot DMF and 20 ml THF. Removed ice bath at 15 minutes and stirred at 25° C. overnight. Stripped solvent, slurried residue with water, and collected solids. Boiled in ethyl acetate, collected solids, and dried in vacuo, giving 735 mg of yellow solid: mass spectrum (electrospray m/e): M+H=363.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-87098cb2b19b40ee9d7db60212ca372b
Source noteuspto-grants-2002_05