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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583101Generated: October 30, 2026

4-Methylmorpholine → N-[3-Cyano-4-[[(dimethylamino)methylene]amino]phenyl]-2-butynamide

https://huagongshe.com/reaction/583101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-Butynoic acidHCID 68535—
ReactantSodium BicarbonateHCID 516892—
Reactant(E)-N'-(4-Amino-2-cyanophenyl)-N,N-dimethylformimidamideHCID 11263933—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductN-[3-Cyano-4-[[(dimethylamino)methylene]amino]phenyl]-2-butynamideHCID 1835069289%

Reaction Steps

To a solution of 2.01 g (23.9 mmol) of 2-butynoic acid and 2.9 ml (22.3 mmol) isobutyl chloroformate in 30 ml tetrahydrofuran was stirred at 0° C. under nitrogen as 2.42 g (2.63 ml, 22.3 mmol) of N-methyl morpholine was added over 3 min. After stirring for 15 min., a solution of N'-(4-amino-2-cyanophenyl)-N,N-dimethylformamidine and 1.6 g (1.75 ml, 15.9 mmol) of N-methyl morpholine in 25 ml tetrahydrofuran was added over 4 min. The mixture was stirred 30 min. at 0° C. and 30 min. at room temperature. The mixture was diluted with 70 ml of ethyl acetate and poured into a mixture of brine and saturated sodium bicarbonate. The organic layer was dried (MgSO4) and filtered through a pad of silica gel. The solvent was removed and the residue was stirred with 50 ml of ether. The suspended solid was collected to give 3.61 g (89%) of an off-white solid. mass spectrum (m/e): 255.0 (M+H, electrospray).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929080
Source datasetuspto-grants-1999_07
ORD IDord-07a9a542b1654bb29ad329e06359b547
Source noteuspto-grants-1999_07