Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Reactant | HCID 53653102 | HCID 53653102 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53665275 | HCID 53665275 | — |
Reaction Steps
3-Methoxybenzyl chloride (1.28 g, 7.5 mol) and Cs2CO3 (5.9 g, 18 mmole) were added to a solution of 1-[1-(3-methoxyphenyl)-3-(1-piperazinyl)-1-propenyl]cyclohexanol (2.0 g, 6 mmole) in DMF (50 mL) and the mixture stirred at room temperature for one hour. Triethylamine (0.25 mL) was then added and the reaction mixture stirred overnight. The solvent was evaporated and the residue dissolved in chloroform. The solution was washed with water and the water back-extracted with chloroform. The combined organic solution was washed with brine, dried over magnesium sulfate and evaporated. The product was purified using column chromatography with chloroform as eluent and the purified title compound was converted to the hydrochloride. Yield 530 mg, m.p. 169°-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04745191 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-41052dc3995240838f0a4fbfebab37c1 |
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| Source note | uspto-grants-1988_05 |
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