Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 10997188 | HCID 10997188 | — |
| Reactant | HCID 21963772 | HCID 21963772 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21963748 | HCID 21963748 | — |
Reaction Steps
A solution of 3-(1-benzenesulphonylcyclopent-3-enyl)propan-1-ol (56 mg, 0.21 mmol) and triethylamine (41 μL, 0.29 mmol) in dichloromethane (5 ml) was cooled to 0° C. and treated with methanesulphonyl chloride (21 μL, 0.27 mmol). The mixture was allowed to warm to room temperature and stirred for 30 minutes, then diluted with water and extracted with ethyl acetate. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The residue was dissolved in acetonitrile (5 ml), treated with 3,4-dimethyl-1,2,5,6-tetrahydropyridine (397 mg, 0.32 mmol) and potassium carbonate (58 mg, 0.42 mmol) and heated at 60° C. for 3 hours. The mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The residue was purified by preparative thin layer chromatography, eluting with 5% methanol/dichloromethane, to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101892B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-0e6f2490dd494bd3b9b642b075fe5097 |
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| Source note | uspto-grants-2006_09 |
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