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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844448Generated: October 30, 2026

Bromoform → 2,6-Dibromo-[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1844448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantDichloroacetic AcidHCID 6597—
ReactantSodium NitriteHCID 23668193—
Reactant6-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215940—
CatalystBenzyltriethylammonium bromideHCID 165294—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,6-Dibromo-[1,2,4]triazolo[1,5-a]pyridineHCID 6839087526%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 6-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine (20.86 g, 97.9 mmol), sodium nitrite (67.6 g, 979 mmol) and benzyltriethylammonium bromide (53.3 g, 196 mmol) in bromoform (1.47 kg, 508 ml, 5.81 mol) was stirred for 30 minutes at 25° C. Then dichloroacetic acid (25.3 g, 16.2 ml, 196 mmol) was added and the mixture was stirred for 20 hours at 25° C. under exclusion of light. 600 ml of water were added to the mixture and stirred for 30 minutes. The mixture was diluted with water and dichloromethane, filtrated over dicalite and the filtrate extracted 3 times with dichloromethane. The organic layers were combined, washed with water, dried over magnesium sulfate, filtrated and evaporated to dryness under reduced pressure. The crude material was purified by flash chromatography in 2 portions over 2×70 g silica columns using dichloromethane/methanol 5% as eluent, affording 2,6-dibromo-[1,2,4]triazolo[1,5-a]pyridine (7 g, 26%) as light brown solid. Mp.: 201° C. MS: m/z=277.7/279.9 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946427B2
Source datasetuspto-grants-2015_02
ORD IDord-fc03e87c4bbc4542b1ab225825813f22
Source noteuspto-grants-2015_02