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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162290Generated: October 28, 2026

4-Chloroaniline → methyl(2R)-4-((4-chlorophenyl)amino)-2-cyclohexyl-4-oxobutanoate

https://huagongshe.com/reaction/1162290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(3R)-3-cyclohexyl-4-methoxy-4-oxobutanoic acidHCID 2734512—
SolventAcetonitrileHCID 6342—
Productmethyl(2R)-4-((4-chlorophenyl)amino)-2-cyclohexyl-4-oxobutanoateHCID 6864702694.5%

Reaction Steps

To a suspension of (3R)-3-cyclohexyl-4-methoxy-4-oxobutanoic acid (0.21 g), 4-chloroaniline (0.13 g) and HOBt (0.23 g) in acetonitrile (10 ml) were added WSC (0.29 g) and N-methylmorpholine (0.10 g), and mixed at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate. The ethyl acetate solution was washed sequentially with an aqueous sodium hydrogen carbonate solution, water, a 5% aqueous citric acid solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain the title compound as a pale brown solid (0.30 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820673B2
Source datasetuspto-grants-2010_10
ORD IDord-6096523440a24c799c599e6733b97686
Source noteuspto-grants-2010_10