HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 749182Erstellt: 24. Oktober 2026
3-(4-Methyl-1-piperazine)propan-1-ol → 5-{[1-(2-tert-butoxyethyl)piperidin-4-yl]oxy}-7-[3-(4-methylpiperazin-1-yl)propoxy]quinazolin-4(3H)-one
https://huagongshe.com/de/reaction/749182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-(4-Methyl-1-piperazine)propan-1-ol | HCID 79208 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | 5-{[1-(2-tert-butoxyethyl)piperidin-4-yl]oxy}-7-fluoroquinazolin-4(3H)-one | HCID 136351952 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | Ammonia | HCID 222 | — |
| Produkt | 5-{[1-(2-tert-butoxyethyl)piperidin-4-yl]oxy}-7-[3-(4-methylpiperazin-1-yl)propoxy]quinazolin-4(3H)-one | HCID 136351951 | 109,2% |
Reaktionsschritte
5-{[1-(2-tert-butoxyethyl)piperidin-4-yl]oxy}-7-fluoroquinazolin-4(3H)-one (5.45 mg, 1.5 mmol) in anhydrous diglyme (15 ml) was reacted with 3-(4-methylpiperazin-1-yl)propan-1-ol (474 mg, 3 mmol) in the presence of potassium tert-butoxide (11.77 g, 10 mmol) at 100° C. for 4 hours. The reaction mixture was diluted with dichloromethane (10 ml) and water (10 ml) and the pH adjusted to 7.7. The mixture was extracted several times with dichloromethane and the organic phase dried (magnesium sulphate), evaporated and the residue purified by chromatography on silica gel. Elution with dichloromethane:methanolic ammonia (9:1) yielded 5-{[1-(2-tert-butoxyethyl)piperidin-4-yl]oxy}-7-[3-(4-methylpiperazin-1-yl)propoxy]quinazolin-4(3H)-one (411 mg, 55% yield):
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07402585B2 |
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| Quelldatensatz | uspto-grants-2008_07 |
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| ORD ID | ord-dbb39fb66c83498ea7f50391fc9ea242 |
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| Quellennotiz | uspto-grants-2008_07 |
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