HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1296596Erstellt: 24. Oktober 2026
4-Thiazoleacetic acid → 3-[2-(4-Nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine
https://huagongshe.com/de/reaction/1296596
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Thiazoleacetic acid | HCID 236262 | — |
| Edukt | 5,6-Diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil | HCID 11609665 | — |
| Produkt | 3-[2-(4-Nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine | HCID 18449501 | — |
Reaktionsschritte
By the method of Example 2, 4-thiazolylacetic acid is reacted with 5,6-diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil (6) to yield 3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine. By the method of Example 3, this substance is alkylated with a mixture of 1,2-dichloroethane, sodium carbonate and 2-(ethylamino)ethanol to yield 7-[2-ethyl(2-hydroxyethyl)amino]ethyl-3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine. By the method of Example 4 this substance is reduced with hydrazine hydrate or hydrogen gas in the presence of a palladium catalyst to yield 3-[2-(4-aminophenyl)ethyl]-7-[2-ethyl(2-hydroxyethyl)amino]ethyl-1-propyl-8-[(4-thiazolyl)methyl]xanthine free base. The corresponding hydrochloride salt is then made on exposure to an excess of hydrogen chloride in solution.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07247639B2 |
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| Quelldatensatz | uspto-grants-2007_07 |
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| ORD ID | ord-89b2d692ba8e427bb8808a782009cd07 |
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| Quellennotiz | uspto-grants-2007_07 |
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