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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
Edukt5-Chloropyrrolo[2,1-f][1,2,4]triazin-4(1H)-oneHCID 135742086—
EduktHCID 178479710HCID 178479710—
LösungsmittelTolueneHCID 1140—
Produkt4,5-Dichloropyrrolo[2,1-f][1,2,4]triazineHCID 2108166967,3%

Reaktionsbedingungen

Temperatur100 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07439246B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-eef68dead9064969a4b2d1a50ede38cd
Quellennotizuspto-grants-2008_10