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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240587Generated: October 31, 2026

Trifluoroacetic acid → 4-([1,2,4]Triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoic acid

https://huagongshe.com/reaction/240587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoateHCID 66937100—
SolventDichloromethaneHCID 6344—
Product4-([1,2,4]Triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoic acidHCID 66937264—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 25 ml flask was charged with tert-butyl 4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoate (0.060 g, 0.16 mmol) and dichloromethane (1.6 ml). The reaction was cooled to 0° C., and 2,2,2-trifluoroacetic acid (0.50 ml, 0.16 mmol) was added. The reaction was stirred for 20 minutes, then warmed to ambient temperature, stirred an additional 3 hours, and then concentrated to provide the desired product as a colorless oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648087B2
Source datasetuspto-grants-2014_02
ORD IDord-71a23a64da1143f1900d1e38a7096dce
Source noteuspto-grants-2014_02