Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(2-Chloroethyl)piperidine | HCID 74827 | — |
| Reactant | 5-Chloro-3-phenyl-1H-indazole | HCID 615118 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Product | HCID 68141719 | HCID 68141719 | 114.4% |
Reaction Steps
3-Phenyl-5-chloroindazole (4.57 g), piperidinoethyl chloride (3.6 g), and triethylbenzylammonium chloride (0.5 g) were added to 50% aqueous sodium hydroxide solution (5 ml) followed by stirring at 70° C for 1 hour. After completion of the reaction, the mixture was extracted with benzene and the extract was washed with water, dried over sodium sulfate and concentrated. The residue was treated with ethanol-hydrochloric acid to obtain 4.3 g of 1-piperidinoethyl-3-phenyl-5-chloroindazole hydrochloride having a melting point between 230°-235° C after recrystallization from acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03994890 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-a957e3923ccb414fb7ac64aa465d1c9e |
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| Source note | uspto-grants-1976_11 |
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