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HRID 569960Erstellt: 25. Oktober 2026
Hydrochloric Acid → 7-{3-[4-(3,4,5-Trimethoxyphenyl)-piperazinyl]propoxy}-3,4-dihydrocarbostyril dihydrochloride
https://huagongshe.com/reaction/569960
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1-(3,4,5-Trimethoxyphenyl)piperazine | HCID 3838765 | — |
| Edukt | 7-(3-Chloropropoxy)-3,4-dihydroquinolin-2(1H)-one | HCID 13053529 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 7-{3-[4-(3,4,5-Trimethoxyphenyl)-piperazinyl]propoxy}-3,4-dihydrocarbostyril dihydrochloride | HCID 12899526 | 61% |
Reaktionsschritte
12.4 Grams of 7-(3-chloropropoxy)-3,4-dihydrocarbostyril, 1 g of pyridine and 2.6 g of 4-(3,4,5-trimethoxyphenyl)piperazine are mixed in 20 ml of dimethylsulfoxide, then stirred at 80°-90° C. for 5 hours. The reaction mixture is poured into 80 ml of 2% aqueous solution of sodium hydrogencarbonate and the organic layer is extracted with chloroform. The chloroform layer is washed with water, dried and chloroform is removed by distillation. The residue thus obtained is dissolved in 30 ml of ethanol and dried hydrogen chloride gas is blown into the ethanol solution. The crystals thus precipitated are collected by filtration and recrystallized from methanol-ethanol to obtain 3.2 g (yield: 61%) of 7-{3-[4-(3,4,5-trimethoxyphenyl)piperazinyl]propoxy}-3,4-dihydrocarbostyril dihydrochloride in the form of colorless needle-like crystals with a melting point of 225°-227° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04734416 |
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| Quelldatensatz | uspto-grants-1988_03 |
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| ORD ID | ord-313bd711b4194964864aa7d800bcb0d7 |
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| Quellennotiz | uspto-grants-1988_03 |
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