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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Methylthio)propanoic acid | HCID 563 | — |
| Reactant | Dehydronorketamine | HCID 162835 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(2-Chlorophenyl)-6-(3-(methylthio)propanoyl)amino-2-cyclohexen-1-one | HCID 9883696 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05384331 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-cb8836e5653742caa26b550d35d68061 |
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| Source note | uspto-grants-1995_01 |
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