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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527248Generated: October 30, 2026

Nitrogen → 2-(2-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)oxazol-4-yl)propan-2-ol

https://huagongshe.com/reaction/527248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67958661HCID 67958661—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(2-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)oxazol-4-yl)propan-2-olHCID 67958765—

Reaction Conditions

Temperature85 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 2-(2-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)oxazol-4-yl)propan-2-ol (2.40 g, 10.75 mmol), iron powder (1.82 g, 32.25 mmol) and NH4Cl (2.90 g, 53.76 mmol) in a mixture of EtOH (70 mL) and water (35 mL) was stirred at 85° C. for 15 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (110 mL) was added followed by 1N NaOH (65 mL). The layers were separated and the aq. layer was extracted with CH2Cl2 (5×50 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as an orange oil. LC-MS-conditions 06: tR=0.35 min; [M+H]+=224.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346793B2
Source datasetuspto-grants-2016_05
ORD IDord-249fc07b6a694ffc9423c8ed9637ac9a
Source noteuspto-grants-2016_05