HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347488Erstellt: 24. Oktober 2026
Dabco → 4-(2-Fluoro-4-nitrophenoxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl pivalate
https://huagongshe.com/de/reaction/347488
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dabco | HCID 9237 | — |
| Edukt | 2-Fluoro-4-nitrophenol | HCID 9825 | — |
| Edukt | 4-Chloro-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl 2,2-dimethylpropanoate | HCID 21081679 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-(2-Fluoro-4-nitrophenoxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl pivalate | HCID 21081648 | — |
Reaktionsschritte
To a homogeneous solution of 4-chloro-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl pivalate (1.00 g, 3.74 mmol, Compound D of Example 1) and 2-fluoro-4-nitrophenol (588 mg, 3.74 mmol) in anhydrous acetonitrile (25 mL), at room temperature under a nitrogen atmosphere, was added DABCO (462 mg, 4.12 mmol). The mixture was then heated at 50° C. for 3 h. The mixture was cooled to room temperature then partitioned between chloroform and saturated aqueous ammonium chloride. The aqueous layer was extracted twice with chloroform. The combined organic layers were washed once each with saturated aqueous ammonium chloride and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated in vacuo to yield a pale yellow solid that was used in the next step without further purification. MS(ESI+) m/z 389.1 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07173031B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-e6d1ae4088f84edeb192d6aab41665dc |
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| Quellennotiz | uspto-grants-2007_02 |
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