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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502648Generated: October 31, 2026

1H-1,2,4-Triazole → HCID 53632732, compound

https://huagongshe.com/reaction/1502648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Acetyl-2-bromopyridineHCID 15668195—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53632732HCID 5363273285%

Reaction Conditions

Temperature100 °C

Reaction Steps

622 mg (corresponding to 9.00 mmol) of 1H-1,2,4-triazole was dissolved in 10 mL of dimethylformamide. Then, 600 mg (corresponding to 3.00 mmol) of 5-acetyl-2-bromopyridine and 1.24 g (corresponding to 9.00 mmol) of potassium carbonate were added thereto. The resulting solution was heated at 100° C. for 3 hours. After the completion of the reaction, the reaction solution was cooled down to room temperature, supplemented with a saturated ammonium chloride aqueous solution and water, and extracted 3 times with dichloromethane. The combined dichloromethane layer was washed with water and a saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (elution solvent: dichloromethane/ethyl acetate=4/1), to obtain 480 mg (corresponding to 2.55 mmol) of 5-acetyl-2-(1H-1,2,4-triazole-1-yl)pyridine (FIG. 4, step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211350B2
Source datasetuspto-grants-2015_12
ORD IDord-cc77916e3ab44b18a0ca0ebf1fd57f7f
Source noteuspto-grants-2015_12