Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605986Generated: October 26, 2026

Methanol → 4-(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamino)-benzoic acid

https://huagongshe.com/reaction/605986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant4-(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamino)-benzoic acid methyl esterHCID 57590027—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamino)-benzoic acidHCID 5759008549%

Reaction Steps

4-(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamino)-benzoic acid methyl ester (460 mg, 1.32 mmol) is suspended in THF (1 mL) and a solution of lithium hydroxide monohydrate (554 mg, 13.2 mmol) in water (11 mL) is added. The reaction mixture is stirred at room temperature for 4 hours then methanol (11 mL) is added and the mixture is stirred at 50° C. for 24 hours. The mixture is partitioned between water and DCM, the aqueous phase is acidified with 2M HCl (pH 2) and a yellow precipitate is formed. The precipitate is collected by filtration, washed with water and diethyl ether and dried to afford the title compound (215 mg, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915256B2
Source datasetuspto-grants-2011_03
ORD IDord-1635e84d076d4791b09a86219e9f2a6b
Source noteuspto-grants-2011_03