Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612069Generated: November 3, 2026

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

https://huagongshe.com/reaction/612069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantTetrahydrofuranHCID 8028—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-Butynoic acidHCID 68535—
Reactant6-Amino-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrileHCID 22466644—
SolventWaterHCID 962—
ProductN-{3-Cyano-[(3-methylphenyl)amino]-6-quinolinyl}-2-butynamideHCID 19598407—

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 numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-f5462a72fd2e4dbfb7e1042a2f819e90
Source noteuspto-grants-1999_12