Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- | HCID 11325 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-((4-Chlorophenyl)(4-piperidinyloxy)methyl)pyridine | HCID 11141197 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 15055857 | HCID 15055857 | 41% |
Reaction Steps
7.50 g (24.77 mmol) of 4-[(4-chlorophenyl)-2-pyridylmethoxy]piperidine and 6.92 g (27.24 mmol) of N-(2-bromoethyl)phthalimide were dissolved in 60 ml of dioxane, and 4.11 g (29.74 mmol) of potassium carbonate was added. The mixture was stirred at an oil bath temperature of 90° to 100° C. for 3 hours. After the reaction, the insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The residue was separated by silica gel column chromatography using a mixture of ethyl acetate and methanol in the volume ratio 25:1 as an eluent. The desired fraction was concentrated under reduced pressure, and 60 ml of ethanol and 1.61 g (32.16 mmol) of hydrazine (hydrate) were added to the residue, and the mixture was stirred under reflux. After 200 ml of 1N aqueous sodium hydroxide was added to the reaction mixture, the mixture was extracted twice with 200 ml of chloroform. The chloroform extract was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 3.50 g (41%) of 2-[4-[(4-chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethylamine as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929618 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-c476f6c0deb44775ab78a4283595b55a |
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| Source note | uspto-grants-1990_05 |
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