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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42826Generated: October 27, 2026

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

https://huagongshe.com/reaction/42826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-[2-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-5-ylmethyl]-4-nitro-2H-[1,2,3]triazoleHCID 67365610—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-[2-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-5-ylmethyl]-2H-[1,2,3]triazol-4-ylamineHCID 67365496—

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 2-[2-(2-methyl-[1,3]dioxolan-2-yl)-thiazol-5-ylmethyl]-4-nitro-2H-[1,2,3]triazole (201 mg, 0.68 mmol), iron powder (114 mg, 2.03 mmol) and NH4Cl (183 mg, 3.38 mmol) in a mixture of EtOH (3.0 mL) and water (1.5 mL) was stirred at 75° C. for 60 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (10 mL) was added followed by 1N NaOH (10 mL). The aq. layer was extracted with CH2Cl2 (2×10 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: TLC:rf (19:1 CH2Cl2-MeOH)=0.2. LC-MS-conditions 02: tR=0.68 min; [M+H]+=268.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-8272a427c31049fcace3deb0e0efbf4a
Source noteuspto-grants-2013_09