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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270303Generated: October 27, 2026

1H-1,2,4-Triazole → HCID 22329661, compound

https://huagongshe.com/reaction/1270303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5,7-Dimethyl-2-(4-nitrophenyl)imidazo[5,1-f][1,2,4]triazin-4(3H)-oneHCID 135553069—
SolventPyridineHCID 1049—
ProductHCID 22329661HCID 22329661—

Reaction Conditions

Temperature20 °C

Reaction Steps

2.53 g (1.54 ml, 16.51 mmol) of phosphoryl chloride are added dropwise under argon to a solution of 1.57 g (5.50 mmol) of 5,7-dimethyl-2-(4-nitrophenyl)imidazo-[5,1-f][1,2,4]triazin-4-(3H)one from example 8A in 10 ml of dry pyridine at 0° C., and the mixture is stirred for 30 min at 20° C. Subsequently, 3.42 g (49.53 mmol) of 1,2,4-triazole are added, and the mixture is stirred overnight at RT. The reaction mixture is concentrated, the residue is treated with aqueous sodium hydrogencarbonate solution, and the mixture is extracted using dichloromethane. The organic phase is dried (sodium sulfate) and the solvent is removed in vacuo. The residue is purified by flash chromatography (eluent: dichloromethane/methanol 100:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202243B2
Source datasetuspto-grants-2007_04
ORD IDord-75882283d6b5424089c3df8e02805699
Source noteuspto-grants-2007_04