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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500805Generated: October 31, 2026

Sulfuric Acid → Ethyl 4-aminopyrrolo[2,1-F][1,2,4]triazine-6-carboxylate

https://huagongshe.com/reaction/1500805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant4-Aminopyrrolo[2,1-F][1,2,4]triazine-6-carbonitrileHCID 55297458—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-aminopyrrolo[2,1-F][1,2,4]triazine-6-carboxylateHCID 66641336—

Reaction Steps

A solution of 4-aminopyrrolo[2,1-f][1,2,4]triazine-6-carbonitrile (3.9 g, 24.5 mmol; preparation described in PCT Int. Pat. Appl. WO 2007/064883) in ethanol (124.8 ml) was stirred with concentrated sulfuric acid (62.4 ml) at 80° C. overnight. After cooling to rt, the reaction mixture was poured onto 800 g of ice and brought to pH 6-7 with concentrated aq. sodium hydroxide solution. Ethyl acetate (500 ml) and dichloromethane (500 ml) were added to the suspension, and the resulting mixture was filtered over kieselguhr. The organic layer was separated from the aqueous layer. The solid was dissolved in hot water (1 L), and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated. The residue was triturated with an isopropanol/diethylether mixture, and the solid was filtered off yielding 2.5 g (49% of th.) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206184B2
Source datasetuspto-grants-2015_12
ORD IDord-2ea6ce13239a4a6bbc6a37c7767bf0e9
Source noteuspto-grants-2015_12