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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hydrazinecarboxaldehyde | HCID 12229 | — |
| Reactant | Methyl 3-[(methylamino)carbonothioyl]-5-(5-methylpyridin-2-yl)benzoate | HCID 86646758 | — |
| Catalyst | Mercurous acetate | HCID 61181 | — |
| Product | Methyl 3-(5-methylpyridin-2-yl)-5-(4-methyl-4H-1,2,4-triazol-3-yl)benzoate | HCID 68498660 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08247401B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-9baf22b7b0d84bc5876adbbcc9991bde |
|---|
| Source note | uspto-grants-2012_08 |
|---|