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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595702Generated: October 29, 2026

Hydrochloric Acid → 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carboxylic acid

https://huagongshe.com/reaction/595702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrileHCID 90332439—
Product6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carboxylic acidHCID 9033251685%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrile (50 mg, 0.14 mmol) in 10% NaOH (5 mL) was heated at 100° C. for 48 h. The reaction mixture was cooled to RT and poured into water (10 mL). After pH was adjusted to 4 with 1 N HCl, the mixture was extracted with EtOAc. The combined organic phases were washed with brine, dried over Na2SO4, filtered and evaporated to get 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carboxylic acid (45 mg, yield: 85%). 1H-NMR (DMSO-d6, 400 MHz) δ 8.20 (s, 1H), 7.77˜7.82 (m, 2H), 7.45˜7.52 (m, 2H), 7.03 (s, 1H), 6.61 (s, 1H), 5.60 (s, 2H). MS (M+H)+: 350/352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243002B2
Source datasetuspto-grants-2016_01
ORD IDord-b049edf44a5a4d9b87609a60b4a7a962
Source noteuspto-grants-2016_01