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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347518Generated: October 26, 2026

Diisopropylethylamine → 4,5-Dichloropyrrolo[2,1-f][1,2,4]triazine

https://huagongshe.com/reaction/347518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Chloropyrrolo[2,1-f][1,2,4]triazin-4(1H)-oneHCID 135742086—
ReactantHCID 178479710HCID 178479710—
SolventTolueneHCID 1140—
Product4,5-Dichloropyrrolo[2,1-f][1,2,4]triazineHCID 2108166967.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173031B2
Source datasetuspto-grants-2007_02
ORD IDord-08333b9b45ba46709d9cde206028d605
Source noteuspto-grants-2007_02