HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066057Generated: November 3, 2026
1-(2-Methoxyphenyl)piperazine → HCID 10202244, compound
https://huagongshe.com/reaction/1066057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21197965 | HCID 21197965 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10202244 | HCID 10202244 | 64% |
Reaction Steps
A suspension containing 2-methoxyphenylpiperazine (1.0 mmole), potassium carbonate (2.0 mmole), potassium iodide (0.5 mmole) and 4-benzyl-5-chloromethyl-2-tertbutyl oxazole (1.0 mmole) from example 4, was stirred in acetone (10 ml) at ambient temperature for three days. The solvent was removed in vacuo, water (50 ml) added and the product extracted into ethyl acetate (3×50 ml). The combined organics were washed with water (50 ml), dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The product was purified by “flash” chromatography over silica gel to afford the titled compound as a colorless oil (0.64 mmole, 64% yield). This was transformed into its mono-fumarate salt, a white crystalline powder, using the procedure outlined in example 10 above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06242448B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-91e3e41691e443fe92152a890cfe915a |
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| Source note | uspto-grants-2001_06 |
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