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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674765Generated: October 25, 2026

Sodium Bicarbonate → 6-Bromo-3-(trifluoromethyl)-(1,2,4)triazolo(4,3-a)pyridine

https://huagongshe.com/reaction/1674765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantN'-(5-bromopyridin-2-yl)-2,2,2-trifluoroacetohydrazideHCID 54363377—
SolventWaterHCID 962—
Product6-Bromo-3-(trifluoromethyl)-(1,2,4)triazolo(4,3-a)pyridineHCID 5811890678.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of polyphosphoric acid (20 mL, 175 mmol) and N′-(5-bromopyridin-2-yl)-2,2,2-trifluoroacetohydrazide (1.9 g, 6.69 mmol) was stirred at 120° C. for 20 hours and then poured in to water. The mixture was then basified with saturated aqueous sodium bicarbonate solution and extracted with dichloromethane (3×250 mL). The organic phases were combined and washed with brine (1×100 mL), dried with MgSO4 and evaporated to give an involatile residue. The residue was purified by flash chromatography on silica-gel using an increasing gradient of ethyl acetate in isohexane as eluant to give 6-bromo-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine (1.39 g, 78%) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-f7a05e46965e4096ac6452a06daf1ade
Source noteuspto-grants-2011_08