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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79022Generated: October 28, 2026

Trifluoroacetic acid → 4-(4-bromo-2-fluorophenylamino)-1H-indazole-5-carboxylic acid

https://huagongshe.com/reaction/79022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-Bromo-2-fluorophenylamino)-indazole-1,5-dicarboxylic acid di-tert-butyl esterHCID 67084035—
SolventDichloromethaneHCID 6344—
Product4-(4-bromo-2-fluorophenylamino)-1H-indazole-5-carboxylic acidHCID 6708409780%

Reaction Steps

To a solution of 4-(4-bromo-2-fluorophenylamino)-indazole-1,5-dicarboxylic acid di-tert-butyl ester (420 mg, 0.83 mmol) in DCM (5 ml) was added TFA (1.2 mL, 16.2 mmol). The reaction mixture was stirred at room temperature for 16 hours before being concentrated in vacuo. The resultant residue was dissolved in ethyl acetate (10 mL), washed with aqueous saturated sodium bicarbonate solution (10 mL) and the aqueous fraction extracted with ethyl acetate (2×10 mL). The combined organic extracts were washed with brine (20 mL), dried with MgSO4 and concentrated in vacuo. The resultant residue was subjected to flash chromatography (Si—PPC, gradient 0-100% ethyl acetate in cyclohexane) to yield the title compound as an off-white solid (232 mg, 80%). LCMS (Method B): RT=3.22 min, [M+H]+=350/352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-c64e35c0315749d79c1bd1abaf1a4a06
Source noteuspto-grants-2014_09