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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13181Generated: October 30, 2026

Hydrochloric Acid → 3-(5-iodo-1H-indazol-1-yl)benzoic acid

https://huagongshe.com/reaction/13181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-(2-(2-Fluoro-5-iodobenzylidene)hydrazinyl)benzoic acidHCID 67041211—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-(5-iodo-1H-indazol-1-yl)benzoic acidHCID 57432097107.4%

Reaction Steps

3-(2-(2-fluoro-5-iodobenzylidene)hydrazinyl)benzoic acid (3.47 g, 9 mmol) and potassium tert. butoxide (2.3 g, 20.5 mmol) was stirred under argon atmosphere in NMP (45 mL) at 150° C. for 30 min. After cooling, the mixture was diluted with water (100 mL), acidified with aqueous HCl (1.7 M) and extracted trice with EtOAc. The combined organic phases were washed twice with water and then with brine. Evaporation of the organic phase afforded crude title compound (3.52 g, quant.) as a light brown, amorphous, gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728030B2
Source datasetuspto-grants-2010_06
ORD IDord-b3f2daa29ad240d2a9685cb893724806
Source noteuspto-grants-2010_06