Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperazine, 1-(3-chloropropyl)-4-phenyl- | HCID 139197 | — |
| Reactant | HCID 13536177 | HCID 13536177 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 13536203 | HCID 13536203 | — |
Reaction Steps
A mixture of methyl 7-methoxy-3-oxo-3,4-dihydro-2H-1,5-benzoxathiepine-4-carboxylate (10 g), 3-(4-phenylpiperazin-1yl)propyl chloride (9.8 g), anhydrous potassium carbonate (6.2 g), potassium iodide (3.0 g) and methyl ethyl ketone (150 ml) was refluxed under heating for 25 hours. After cooling, inorganic matter was filtered off and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed with water and dried. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=3:1) to give methyl 7-methoxy-3-oxo-4-[3-(4-phenylpiperazine-1-yl)propyl]-3,4-dihydro-2H-1,5-benzoxathiepine-4-carboxylate. Recrystallization from methanol yielded white crystals, melting point 110°-112° C., yield 2.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05538974 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-0f5f7f9e8a774239b1fa7191e6a11c02 |
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| Source note | uspto-grants-1996_07 |
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