HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-[4-(3-Methoxybenzyl)-1-piperazinyl]-2,4,6-cycloheptatriene-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Reactant | 2-(1-Piperazinyl)-2,4,6-cycloheptatrien-1-one acetate | HCID 19599725 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[4-(3-Methoxybenzyl)-1-piperazinyl]-2,4,6-cycloheptatriene-1-one | HCID 15871342 | — |
Reaction Steps
A mixture of 2-(1-piperazinyl)-2,4,6-cycloheptatriene-1-one acetic acid salt (0.171 g, 0.680 mmol, example 2a), 3-methoxybenzyl chloride (0.118 g, 0.750 mmol) and potassium carbonate (0.276 g, 2.00 mmol) in acetonitrile (2.00 mL) was stirred at room temperature for 16 h. The solvent was removed in vacuo. The residue was triturated with dichloromethane and filtered. The filtrate was concentrated in vacuo to dryness and the residue was subjected to preparative thin layer chromatography using ethyl acetate:methanol (9:1) as the eluent. The title compound was obtained as a yellow oil (0.095 g, 45%); MS (FAB) 311 (M+ +1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998414 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-b279790288f442a7accbf291ee6677ac |
| Source note | uspto-grants-1999_12 |