HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256664Erstellt: 25. Oktober 2026
1-Bromo-1-propene → 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine
https://huagongshe.com/reaction/256664
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Bromo-1-propene | HCID 11533 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine | HCID 19785343 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine | HCID 19785242 | 22% |
Reaktionsschritte
A mixture of 1.2 parts of bromo-1-propene, 3.26 parts of 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine, 1.5 parts of sodium hydrogen carbonate and 40 parts of ethanol was stirred for 1 hour at reflux temperature. The reaction mixture was filtered over diatomaceous earth while hot and the filtrate was evaporated. The residue was taken up in water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 0.8 parts (22%) of 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine; mp. 144.8° C. (compound 120).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05258380 |
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| Quelldatensatz | uspto-grants-1993_11 |
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| ORD ID | ord-6a068b16c7e5448499de677d54ff443f |
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| Quellennotiz | uspto-grants-1993_11 |
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