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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934984Generated: November 1, 2026

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

https://huagongshe.com/reaction/1934984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-Butynoic acidHCID 68535—
Reactant6-Amino-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrileHCID 22466644—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-{3-Cyano-4-[(3-methylphenyl)amino]-6-quinolinyl}-2-butynamideHCID 2246659241.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolved 597 mg (7.10 mmol) 2-butynoic acid in 25 ml THF under N2 and chilled to 0° C. Added 950 μl (7.30 mmol) isobutyl chloroformate and 780 μl (7.10 mmol) N-methylmorpholine and stirred for 10 minutes. Added dropwise a solution of 778 mg (2.84 mmol 6-amino-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrile, stirred for 15 minutes at 0° C. and then at 25° C. overnight. Stripped solvent and slurried residue with water, drying the gummy solid in vacuo briefly. Boiled solid in ethyl acetate and collected. Recrystallized from DMF, using ethanol to crash out the product, and dried in vacuo, giving 401 mg of yellow-brown solid: mass spectrum (electrospray m/e): M+H=341.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-6b606a50aada4af1944e18659b1d1d21
Source noteuspto-grants-2002_05