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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888383Generated: November 1, 2026

Tetrahydrofuran → Methyl 3-(5-methylpyridin-2-yl)-5-(4-methyl-4H-1,2,4-triazol-3-yl)benzoate

https://huagongshe.com/reaction/888383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHydrazinecarboxaldehydeHCID 12229—
ReactantMethyl 3-[(methylamino)carbonothioyl]-5-(5-methylpyridin-2-yl)benzoateHCID 86646758—
CatalystMercurous acetateHCID 61181—
ProductMethyl 3-(5-methylpyridin-2-yl)-5-(4-methyl-4H-1,2,4-triazol-3-yl)benzoateHCID 68498660—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of methyl 3-[(methylamino)carbonothioyl]-5-(5-methylpyridin-2-yl)benzoate (0.90 g, 3.00 mmol) in THF (30 mL) was added formic hydrazide (0.54 g, 8.99 mmol) and mercury acetate (1.72 g, 5.39 mmol) and the mixture heated to 40° C. After 16 h, the reaction was cooled to ambient temperature, filtered and concentrated. The organic residue was dissolved in 100 ml of dichloromethane and washed with 50 mL of saturated aqueous sodium bicarbonate (2×). The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (100% dichloromethane→90% dichloromethane/methanol) to give the title compound (0.37 g). MS 309.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-9baf22b7b0d84bc5876adbbcc9991bde
Source noteuspto-grants-2012_08