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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503157Generated: October 30, 2026

Water → 3-(3-Fluoro-phenyl)-6-methoxy-1H-indazole-5-carbonitrile

https://huagongshe.com/reaction/503157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Fluoro-5-(3-fluoro-benzoyl)-2-methoxy-benzonitrileHCID 22261035—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Fluoro-phenyl)-6-methoxy-1H-indazole-5-carbonitrileHCID 22260780—

Reaction Steps

A total of 203 mg of 4-fluoro-5-(3-fluoro-benzoyl)-2-methoxy-benzonitrile obtained in Production Example II-1-c was dissolved in 3 ml of tetrahydrofuran and 3 ml of methanol, 7.4 ml of hydrazine monohydrate was added at room temperature under stirring, and the mixture was stirred at room temperature for 14 hours. Then, water was added and the mixture was extracted with ethyl acetate. The resulting organic layer was washed with 1 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and brine, dried over magnesium sulfate and the solvent was evaporated. The resulting crystals were washed with diethyl ether, to give 172 mg of the title compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776890B2
Source datasetuspto-grants-2010_08
ORD IDord-7b01830d492b4a1b800c43e578609885
Source noteuspto-grants-2010_08