Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692706Generated: October 26, 2026

Hydrochloric Acid → 6-Nitro-1H-indazole-3-carboxylic acid

https://huagongshe.com/reaction/1692706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant6-NitroindazoleHCID 24239—
Reactant6-Nitro-1h-indazole-3-carbonitrileHCID 66932591—
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178526460HCID 178526460—
SolventSodium HydroxideHCID 14798—
Product6-Nitro-1H-indazole-3-carboxylic acidHCID 23118859—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 5 mL microwave reaction vessel was charged with 3-iodo-6-nitroindazole (1 mmol), copper (I) cyanide (2 mmol) and N,N-dimethylformamide (3 mL). The vessel was sealed and subjected to microwave irradiation at 185° C. for 600 sec. The reaction mixture was partitioned between ethyl acetate (100 mL) and water (100 mL) and the mixture was filtered through Celite. The organic layer was collected, washed with brine, dried (magnesium sulfate), and concentrated to give 122 mg of a 10/1 mixture of 3-cyano-6-nitroindazole and 6-nitroindazole as a yellow solid. The 10/1 mixture of 3-cyano-6-nitroindazole and 6-nitroindazole was dissolved in 10 N sodium hydroxide and the bright orange solution was heated at 100° C. for 1 h. The mixture was allowed to cool to room temperature and carefully acidified (pH=1) with 3 N hydrochloric acid. The solid was isolated and triturated with EtOAc to provide 51 mg of 6-nitroindazole-3-carboxylic acid as a brown solid. The acid was coupled with the bicyclobase according to procedure A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158629B2
Source datasetuspto-grants-2012_04
ORD IDord-05d8865635734335a040d3b2d67041fa
Source noteuspto-grants-2012_04