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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022104Generated: November 2, 2026

Ethanol → [1,2,4]Triazolo[1,5-a]pyrazin-2-amine

https://huagongshe.com/reaction/1022104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantEthyl [(pyrazin-2-yl)carbamothioyl]carbamateHCID 15619487—
SolventMethanolHCID 887—
Product[1,2,4]Triazolo[1,5-a]pyrazin-2-amineHCID 1303326692%

Reaction Conditions

Temperature65 °C

Reaction Steps

A 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 270a (6.00 g, 26.43 mmol, 1.0 eq.), hydroxylamine hydrochloride (3.32 g, 47.52 mmol, 1.8 eq.), DIPEA (12 mL), ethanol (40 mL), and methanol (40 mL). The reaction mixture was stirred at 65° C. for 16 hours. After the reaction was complete, it was cooled to room temperature and concentrated to a volume of around 20 mL under reduced pressure. The resulting suspension was collected by filtration and the solid was washed with 60:1 dichloromethane/ethanol (50 mL) to afford 270b (3.3 g, 92%) as a white solid. MS-ESI: [M+H]+ 136.3. 1H NMR (500 MHz, DMSO-d6) δ 8.84 (d, J=1.0 Hz, 1H), 8.70 (dd, J=1.0, 4.0 Hz, 1H), 7.98 (d, J=5.0 Hz, 1H), 6.47 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716274B2
Source datasetuspto-grants-2014_05
ORD IDord-3a86f701399546ccb50441172eeca419
Source noteuspto-grants-2014_05