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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42755Generated: October 26, 2026

Nitrogen → 2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-2H-[1,2,3]triazol-4-ylamine

https://huagongshe.com/reaction/42755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67366415HCID 67366415—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-2H-[1,2,3]triazol-4-ylamineHCID 67365175—

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-[5-(2-methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-4-nitro-2H-[1,2,3]triazole (1.09 g, 3.68 mmol), iron powder (623 mg, 11.05 mmol) and NH4Cl (995 mg, 18.41 mmol) in a mixture of EtOH (10.0 mL) and water (5.0 mL) was stirred at 85° C. for 20 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (30 mL) was added followed by 1M NaOH (20 mL). The aq. layer was extracted with CH2Cl2 (2×20 mL) and 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 02: tR=0.78 min; [M+H]+=267.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-fd9be9393b57491bb46c3d992705c236
Source noteuspto-grants-2013_09