HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40205Erstellt: 23. Oktober 2026
Nitroethane → Tert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate
https://huagongshe.com/de/reaction/40205
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Nitroethane | HCID 6587 | — |
| Edukt | Phenyl isocyanate | HCID 7672 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | tert-Butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate | HCID 57691050 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | Tert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate | HCID 57691036 | — |
Reaktionsschritte
To a solution of nitroethane (1.02 ml, 14.3 mmol) in benzene (50 mL) was added phenyl isocyanate (3.12 ml, 28.5 mmol). The mixture was stirred at 50° C. for twenty minutes followed by the addition of tert-butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate (3.00 g, 11.0 mmol) and triethylamine (0.0765 ml, 0.549 mmol). The mixture was stirred at 50° C. for six hours then at room temperature overnight. The mixture was cooled to room temperature, filtered and the resulting brown precipitate was washed with additional benzene. The filtrate was concentrated to yield the product as a black solid. MS m/z=331.1 [M+1]+. Calc'd for C15H18N6O3: 330.1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524900B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-d952825d729b4d20be4a45b727aa6332 |
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| Quellennotiz | uspto-grants-2013_09 |
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