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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79024Generated: October 29, 2026

Trifluoroacetic acid → 4-(2-Fluoro-4-iodophenylamino)-1H-indazole-5-carboxylic acid

https://huagongshe.com/reaction/79024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(2-Fluoro-4-iodophenylamino)-indazole-1,5-dicarboxylic acid di-tert-butyl esterHCID 67083879—
SolventDichloromethaneHCID 6344—
Product4-(2-Fluoro-4-iodophenylamino)-1H-indazole-5-carboxylic acidHCID 5752150584%

Reaction Steps

To a solution of 4-(2-fluoro-4-iodophenylamino)-indazole-1,5-dicarboxylic acid di-tert-butyl ester (611 mg, 1.10 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 fractions were washed with brine (20 mL), dried (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 (367 mg, 84%). LCMS (Method B): RT=3.23 min, [M+H]+=398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-348b4b1b2602401fa4931da87b982024
Source noteuspto-grants-2014_09