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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769992Generated: October 30, 2026

3-(Methylthio)propanoic acid → 6-(2-Chlorophenyl)-6-(3-(methylthio)propanoyl)amino-2-cyclohexen-1-one

https://huagongshe.com/reaction/1769992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylthio)propanoic acidHCID 563—
ReactantDehydronorketamineHCID 162835—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product6-(2-Chlorophenyl)-6-(3-(methylthio)propanoyl)amino-2-cyclohexen-1-oneHCID 988369665%

Reaction Steps

A solution of 6-amino-6-(2-chlorophenyl)-2-cyclohexen-1-one (50 mg, 0.23 mmol), 3(methylthio)propanoic acid (prepared by the known base hydrolysis from the commercial methyl ester)(33 mg, 0.28 mmol), hydroxybenzotriazole (31 mg, 0.23 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (66 mg, 0.35 mmol) in dimethylformamide (1 ml) was stirred at room temperature for 18 h. The reaction was partitioned between saturated bicarbonate and ethyl acetate, the organic phase was washed with brine, dried (Na2SO4), and the solvent removed by evaporation. Purification was achieved by preparative thin layer chromatography on silica gel eluting with 1:1 ethyl acetate/hexane. Isolation of the UV active band at Rf 0.4 gave 6-(2-chlorophenyl)-6-(3-(methylthio)propanoyl)amino-2-cyclohexen- 1-one (60.6 mg, 65%). The title compound was found to be active at 6μm in the CMK assay.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05384331
Source datasetuspto-grants-1995_01
ORD IDord-cb8836e5653742caa26b550d35d68061
Source noteuspto-grants-1995_01