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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205721Generated: October 30, 2026

Trimethylorthoacetate → 6-Bromo-3-methyl-8-nitro-[1,2,4]triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/2205721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylorthoacetateHCID 21927715—
Reactant5-Bromo-2-hydrazinyl-3-nitropyridineHCID 26370200—
Product6-Bromo-3-methyl-8-nitro-[1,2,4]triazolo[4,3-a]pyridineHCID 58118967—

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 5-bromo-3-nitro-2-hydrazinopyridine (2.0 g, 8.58 mmol) in trimethylorthoacetate (20 mL) was heated at 80° C. for 20 h. After cooling, the solvent was distilled off, the residue was dissolved in ethyl acetate (200 mL), washed with water, brine, dried over sodium sulphate and concentrated to provide the product 6-bromo-3-methyl-8-nitro-[1,2,4]triazolo[4,3-a]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371329B2
Source datasetuspto-grants-2016_06
ORD IDord-f312f9259f004748b279a8779cb13d7e
Source noteuspto-grants-2016_06