HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79481Erstellt: 23. Oktober 2026
Acetylcysteamine → 7-(2-acetamidoethylthio)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide
https://huagongshe.com/de/reaction/79481
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetylcysteamine | HCID 14484 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | 7-Fluoro-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 67259826 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 7-(2-acetamidoethylthio)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 68333440 | 58,3% |
Reaktionsschritte
N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-fluoroimidazo[1,2-a]pyridine-3-carboxamide (0.028 g, 0.065 mmol) (Example 74, Step A), N-(2-mercaptoethyl)acetamide (0.078 g, 0.65 mmol), and potassium tert-butoxide (0.022 g, 0.20 mmol) were added to a minimal amount of deoxygenated 1,4-dioxane in a sealed tube and heated for 18 hours at 95° C. The reaction mixture was cooled, concentrated under reduced pressure and purified by silica gel chromatography eluting with methanol (containing 6% ammonium hydroxide) and dichloromethane (1:9), to yield the product (20 mg) as a white powder. MS ESI (+) m/z 528 (M+1) detected.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841455B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-667f07dc02a9466c8e3966d61737eb20 |
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| Quellennotiz | uspto-grants-2014_09 |
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