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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Aminopyrrolo[2,1-F][1,2,4]triazine-6-carbonitrile | HCID 55297458 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-aminopyrrolo[2,1-F][1,2,4]triazine-6-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206184B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2ea6ce13239a4a6bbc6a37c7767bf0e9 |
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| Source note | uspto-grants-2015_12 |
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