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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42780Generated: October 27, 2026

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

https://huagongshe.com/reaction/42780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridineHCID 67363839—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-[4-(2-Methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl]-2H-[1,2,3]triazol-4-ylamineHCID 67365192—

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-(2-methyl-[1,3]dioxolan-2-yl)-2-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridine (210 mg, 0.71 mmol), iron powder (120 mg, 2.12 mmol) and NH4Cl (191 mg, 3.53 mmol) in a mixture of EtOH (2.0 mL) and water (1.0 mL) was stirred at 75° C. for 1 h. The reaction mixture was filtered while hot and the filter cake rinsed with EtOH. The filtrate was concentrated under reduced pressure and the residue partitioned between CH2Cl2 (10 mL) and aq. 1M NaOH (10 mL). The aq. layer was extracted with CH2Cl2 (2×10 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvent removed under reduced pressure. Purification of the residue by FC (99:1 to 19:1 CH2Cl2-MeOH) gave the title compound as a brown oil: TLC:rf (19:1 CH2Cl2-MeOH)=0.33. LC-MS: tR=0.64 min, [M+H]+=262.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-5dc9d0ccf24a4d0cb69f7af87132726a
Source noteuspto-grants-2013_09