HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329402Generated: October 29, 2026
1-(1-Naphthyl)piperazine → HCID 14727008, compound
https://huagongshe.com/reaction/329402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(1-Naphthyl)piperazine | HCID 1342 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 14726987 | HCID 14726987 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 14727008 | HCID 14727008 | — |
Reaction Steps
To a 125 ml round-bottomed flask equipped with condenser and N2 inlet were added 2.50 g (7.5 mmol) of 4-(4-(2-chloroethyl)phenyl)-2-methylaminothiazole hydrobromide, 1.59 g (7.5 mmol) of N-(1-naphthyl)piperazine, 1.31 ml (7.5 mmol) of diisopropylethylamine, 1.59 g (15 mmol) of sodium carbonate, 5 mg of sodium iodide, and 50 ml of methylisobutylketone. The reaction was heated at reflux for 4 days, cooled, and the precipitate filtered, and the filtrate evaporated. The residue was taken up in methylene chloride and chromatographed on silica gel using methylene chloride/ethyl acetate as eluent to give an oil. The oil was taken up in methylene chloride, precipitated by addition of methylene chloride saturated with hydrochloride, and the precipitate filtered, washed with ether, and dried to give a white solid, m.p. 272°-273° C., 2.37 g (63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04891375 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-f36e3fc9d03147d98d3252b1eaf16f60 |
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| Source note | uspto-grants-1990_01 |
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