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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921342Generated: October 31, 2026

1H-1,2,4-Triazole → HCID 58808788, compound

https://huagongshe.com/reaction/1921342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-5-ethyl-6-methoxy-2-methylpyridineHCID 11658669—
CatalystCopper iodideHCID 83717—
ProductHCID 58808788HCID 5880878819%

Reaction Conditions

Temperature180 °C

Reaction Steps

Into a microwave vial is added 3-bromo-5-ethyl-6-methoxy-2-methyl-pyridine (400 mg, 1.74 mmol), potassium carbonate (360 mg, 2.61 mmol), copper iodide (50 mg, 0.263 mmol) and 1,2,4-triazole (240 mg, 3.47 mmol). The vial is flushed with N2 before anhydrous dimethylformamide (5 mL) is added and then sealed. The reaction is heated in the CEM Discover microwave at 180° C. for 40 minutes. LC/MS shows the reaction is incomplete. Further 1,2,4-triazole (120 mg) and copper iodide (30 mg) are added, the reaction flushed with N2 and is re-microwaved to 180° C. Initially the pressure limit of 20 bar is reached and the process is aborted. The residual pressure is released and the reaction is re-microwaved to 180° C. for 40 min with a maximum pressure of 9-11 bar attained. LC/MS shows the reaction to be complete. The reaction is diluted and extracted with 11 portions of dichloromethane. The combined extracts are then dried over magnesium sulfate and evaporated to give a dark oil. The crude product is purified by flash chromatography on a 5-gram silica gel cartridge by elution with dichloromethane:methanol (19:1). Clean fractions containing the product are combined, the solvent evaporated, and the residue is further purified by flash chromatography on a 5-gram silica gel cartridge by elution with heptane:ethyl acetate (19:1) then dichloromethane:heptane (1:1, increasing to 1:0). Clean fractions containing the product are combined and evaporated to give an orange residue. The product is triturated with ether/heptane to give 3-ethyl-6-methyl-5-(1,2,4-triazol-1-yl)-1H-pyridin-2-one as an orange powder (67 mg, 19% yield). This material (57 mg) is suspended in dichloromethane (2 mL) and treated with ethereal hydrochloric acid (2.0 M, 0.444 mL). The mixture is stirred for 1.5 h and then evaporated to give 3-ethyl-6-methyl-5-1,2,4-triazol-1-yl-1H-pyridin-2-one hydrochloride (70 mg) as a cream-orange solid. LC/MS: RT: 1.79 min, MS: m/e=205 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173682B2
Source datasetuspto-grants-2012_05
ORD IDord-4b11d280f9cc44d4a0bb4859dcc386aa
Source noteuspto-grants-2012_05