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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595701Generated: October 30, 2026

Water → 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrile

https://huagongshe.com/reaction/595701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-bromo-2-(4-fluorophenyl)-6-nitro-2H-indazole-3-carbonitrileHCID 67777347—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
Product6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrileHCID 9033243968%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 5-bromo-2-(4-fluorophenyl)-6-nitro-2H-indazole-3-carbonitrile (500 mg, 139 mmol) in a mixture of methanol (50 mL), THF (5 mL) and water (2.5 mL) was added ammonium chloride (370 mg, 6.91 mmol) followed by iron powder (386 mg, 6.91 mmol). The mixture was heated to 80° C. and stirred vigorously for 90 min. The resulting suspension was filtered through celite and washed with EtOAc. The filtrate was concentrated, and the residue was suspended in water and extracted with EtOAc. The organic layer was contracted to give 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrile (310 mg, 68%) as a yellow solid. 1H-NMR (CDCl3, 400 MHz) δ 7.99 (s, 1H), 7.80˜7.82 (m, 2H), 7.23˜7.57 (m, 2H), 7.03 (s, 1H), 4.40 (s, 2H). MS (M+H)+: 331/333.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243002B2
Source datasetuspto-grants-2016_01
ORD IDord-55771fbc1eb346fb89c915faa9bb3afe
Source noteuspto-grants-2016_01