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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82824Generated: October 30, 2026

Nitrogen → 2-((2-(2-methoxypropan-2-yl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-amine

https://huagongshe.com/reaction/82824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67958055HCID 67958055—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-((2-(2-methoxypropan-2-yl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-amineHCID 67957927—

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-methoxypropan-2-yl)-4-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)oxazole (33 mg, 0.12 mmol), iron powder (21 mg, 0.37 mmol) and NH4Cl (33 mg, 0.62 mmol) in a mixture of EtOH (0.4 mL) and water (0.2 mL) was stirred at 85° C. for 30 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (5 mL) was added followed by 1N NaOH (5 mL). The layers were separated and the aq. layer was extracted with CH2Cl2 (5×5 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure to give the title compound as an orange oil. LC-MS-conditions 07: tR=0.51 min; [M]+=237.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-90d968fbbf284efeab0f054d2003ab1d
Source noteuspto-grants-2014_09