Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Methylbenzyl chloride | HCID 7722 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 6-(piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-one | HCID 11117896 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21472303 | HCID 21472303 | 18.1% |
Reaction Steps
To a mixture of 1.2 g of 6-(1-piperazinyl)-3,4-dihydrocarbostyril, 1.17 g of potassium bicarbonate and 20 ml of DMF was added 646 mg of 4-methylbenzyl chloride and the mixture was stirred at 80° C. for 2.5 hours. The reaction mixture was poured into a large amount of water and extracted with chloroform. After washing with water the extract was dried over anhydrous sodium sulfate. Chloroform was distilled off and the residue was purified through silica gel column chromatography. After conversion to hydrochloric acid salt with methanol-hydrochloric acid, the product was recrystallized from methanol-water to give 0.17 g of 6-[4-(4-methylbenzyl)-1-piperazinyl]-3,4-dihydrocarbostyril dihydrochloride, m.p. 272°-273° C. (decomp.), colorless powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04415572 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-a00be88f49d7444d91c2c9988a98cd03 |
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| Source note | uspto-grants-1983_11 |
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