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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62016Generated: October 28, 2026

Pyridine → HCID 68702137, compound

https://huagongshe.com/reaction/62016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-(2H-tetrazol-5-yl)-2-(trifluoromethyl)pyridineHCID 68704491—
Reactant3,4-Dimethoxy-N-methyl-5-nitro-benzimidoyl chlorideHCID 86643107—
ProductHCID 68702137HCID 68702137—

Reaction Conditions

Temperature82.5 °C

Reaction Steps

3,4-Dimethoxy-N-methyl-5-nitro-benzimidoyl chloride (0.28 g, 1.08 mmol) was added to a stirred solution of 3-(2H-tetrazol-5-yl)-2-(trifluoromethyl)pyridine (0.215 g, 1 mmol) in dry pyridine (3 mL), preheated to 50° C. The resulting mixture was cautiously heated to 75-90° C. and maintained at this temperature until nitrogen evolution ceased. The mixture was then poured onto water (30 mL) and extracted with dichloromethane (25 mL). The organic phase was separated, dried over anhydrous magnesium sulphate, filtered and evaporated to dryness. The resulting residue was purified by chromatography to afford 3-(5-(3,4-dimethoxy-5-nitrophenyl)-4-methyl-4H-1,2,4-triazol-3-yl)-2-(trifluoromethyl)pyridine, 0.241 g (59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446012B2
Source datasetuspto-grants-2016_09
ORD IDord-993bd659aac04887bd24f303e3591b9f
Source noteuspto-grants-2016_09