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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610113Generated: October 30, 2026

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

https://huagongshe.com/reaction/1610113

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 numberUS06982274B2
Source datasetuspto-grants-2006_01
ORD IDord-514179d23b8a4d23bbea8dd86b3e20d7
Source noteuspto-grants-2006_01