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HRID 2117124Erstellt: 25. Oktober 2026
Diisopropylethylamine → 4,5-Dichloropyrrolo[2,1-f][1,2,4]triazine
https://huagongshe.com/reaction/2117124
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 5-Chloropyrrolo[2,1-f][1,2,4]triazin-4(1H)-one | HCID 135742086 | — |
| Edukt | HCID 178479710 | HCID 178479710 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4,5-Dichloropyrrolo[2,1-f][1,2,4]triazine | HCID 21081669 | 67,3% |
Reaktionsschritte
To a solution of 5-chloropyrrolo[2,1-f][1,2,4]triazin-4(3H)-one (5.00 g, 29.5 mmol) in toluene (100 mL) at rt under nitrogen was added diisopropylethylamine (5.14 mL, 29.5 mmol) followed by phosphorus(III) oxychloride (8.25 mL, 88.5 mmol). The mixture was heated at 100° C. for 20 h and was then cooled to rt. The reaction was slowly added to saturated aqueous sodium bicarbonate solution (500 mL) at 0° C. After the addition was complete, the mixture was stirred at rt for 30 min. The aqueous phase was extracted with ethyl acetate (3×500 mL), dried over anhydrous MgSO4, and concentrated in vacuo to give the crude product (3.73 g, 67%) as a yellow solid which was used without further purification. 1H NMR (CDCl3) δ 8.03 (s, 1H), 7.70 (d, 1H, J=2.8 Hz), 6.84 (d, 1H, J=2.8 Hz); MS(ESI+) m/z 188.1 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07439246B2 |
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| Quelldatensatz | uspto-grants-2008_10 |
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| ORD ID | ord-eef68dead9064969a4b2d1a50ede38cd |
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| Quellennotiz | uspto-grants-2008_10 |
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