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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467313Generated: October 30, 2026

Hydrochloric Acid → 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acid

https://huagongshe.com/reaction/1467313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylateHCID 67984978—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
Product3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acidHCID 6798497598.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a sealed flask was added ethyl 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylate (420 mg, 0.802 mmol), MeOH (6 ml), and sodium hydroxide (1N in water, 4 ml, 4.00 mmol). The resulting mixture was then heated for 60 min at a temperature of 80° C. with stirring. The mixture was then neutralized with HCl (2N in water), diluted with 10% isopropanol in chloroform, washed with water, dried with sodium sulfate, filtered, and concentrated to afford 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acid (392 mg, 0.791 mmol) as a light yellow solid. The crude product was progressed to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999957B2
Source datasetuspto-grants-2015_04
ORD IDord-7fe3d1c8fcca471b8d6273e8759085f1
Source noteuspto-grants-2015_04