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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82810Generated: October 30, 2026

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

https://huagongshe.com/reaction/82810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67958070HCID 67958070—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-((4-(methoxymethyl)thiazol-2-yl)methyl)-2H-1,2,3-triazol-4-amineHCID 67958499—

Reaction Conditions

Temperature75 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 4-(methoxymethyl)-2-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)thiazole (85 mg, 0.31 mmol), iron powder (66 mg, 1.17 mmol) and NH4Cl (108 mg, 2.0 mmol) in a mixture of EtOH (2.0 mL) and water (1.0 mL) was stirred at 75° C. for 25 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (15 mL) was added followed by 1N NaOH (10 mL). The layers were separated and the aq. layer was extracted with CH2Cl2 (3×10 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=0.47 min, [M+H]+=226.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-381a301b268240e5a83a571f6437d33f
Source noteuspto-grants-2014_09