Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(1-Hydroxy-3-chloropropyl)-3,4-dihydrocarbostyril | HCID 20229459 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 13120854 | HCID 13120854 | — |
Reaction Steps
2.6 Grams of 6-(1-hydroxy-3-chloropropyl)-3,4-dihydrocarbostyril and 1.8 g of sodium iodide were mixed in 60 ml of dimethylformamide and the mixture was stirred at a room temperature for 7 hours. Then 2.0 g of triethylamine and 2.5 g of 4-phenylpiperidine were added to the mixture and stirred at a room temperature for 24 hours. The reaction mixture was poured into 200 ml of 1%-sodium hydrogen-carbonate aqueous solution and was extracted with chloroform. The chloroform layer was washed with water and dried, chloroform was removed by distillation. The residue thus obtained was recrystallized from ethanol to obtain 2.5 g of 6-[1-hydroxy-3-(4-phenyl-1-piperidyl)propyl]-3,4-dihydro-carbostyril in colorless plate-like crystals. Melting point: 155.5°-156.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04619932 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-1f76fd506c7445eea970521b24d3a38a |
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| Source note | uspto-grants-1986_10 |
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