Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82806Generated: October 29, 2026

Nitrogen → 2-((5-(methoxymethyl)thiophen-2-yl)methyl)-2H-1,2,3-triazol-4-amine

https://huagongshe.com/reaction/82806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67957844HCID 67957844—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-((5-(methoxymethyl)thiophen-2-yl)methyl)-2H-1,2,3-triazol-4-amineHCID 67958220—

Reaction Conditions

Temperature50 °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-((5-(methoxymethyl)thiophen-2-yl)methyl)-4-nitro-2H-1,2,3-triazole (169 mg, 0.67 mmol), iron powder (131 mg, 2.33 mmol) and NH4Cl (215 mg, 3.99 mmol) in a mixture of EtOH (4.6 mL) and water (2.4 mL) was stirred at 50° C. for 30 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (20 mL) was added followed by 3N NaOH (5 mL). The layers were separated and the aq. layer was extracted with CH2Cl2 (3×15 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a yellow oil. LC-MS-conditions 07: tR=0.58 min, [M+H]+=225.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-0efe5582fe3849faba3102ae42cd0bb5
Source noteuspto-grants-2014_09