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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098938Generated: October 25, 2026

Hydrochloric Acid → 4-(5-Iodoindazole-1-yl)-benzoic acid

https://huagongshe.com/reaction/1098938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(2-(2-Fluoro-5-iodobenzylidene)hydrazinyl)benzoic acidHCID 66812922—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(5-Iodoindazole-1-yl)-benzoic acidHCID 5933974594.1%

Reaction Steps

4-(2-(2-fluoro-5-iodobenzylidene)hydrazinyl)benzoic acid (141d, 3.42 g, 8.9 mmol) and potassium tert-butoxide (2.29 g, 20.5 mmol) was stirred under argon atmosphere in NMP (45 mL) at 150° C. for 15 min. The mixture was then cooled, diluted with water and acidified with aqueous HCl (1.7 M). The precipitate that formed was collected by filtration and dried in vacuo to give crude 4-(5-iodo-1H-indazol-1-yl)benzoic acid (3.05 g, 94%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143290B2
Source datasetuspto-grants-2012_03
ORD IDord-84f9184691b14b6ca0ce1005968e7d52
Source noteuspto-grants-2012_03