Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14627584 | HCID 14627584 | — |
| Reactant | Water methylene chloride | HCID 21908982 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18958819 | HCID 18958819 | — |
Reaction Steps
A suspension prepared by mixing 1 g of 1-methyl-8-amino-3,4-dihydrocarbostyril, 1.35 g of 1,4-dibromobutane, 1.9 g of sodium iodide, 1.75 g of potassium carbonate in 10 ml of acetonitrile was refluxed by heating for 20 hours. Then to the reaction mixture was added dichloromethane-water, and the organic layer was collected by separation, washed with water, and dried with anhydrous sodium sulfate. Next, the solvent was removed by evaporation, and the residue thus obtained was purified by a silica gel column chromatography (eluent: dichloromethane:methanol=50:1). The purified product was dissolved in diethyl ether, and the desired product was converted into hydrochloride by using ethanol-concentrated hydrochloric acid, recrystallized from ethanol-diethyl ether to obtain 1.15 g of 1-methyl-8-pyrrolidino-3,4-dihydrocarbostyril hydrochloride. White powdery substance. Melting point: 174.5°-177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05358949 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-17ce8d74721e42b18787914452eeccb2 |
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| Source note | uspto-grants-1994_10 |
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