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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563431Generated: October 27, 2026

Benzonitrile, 4-bromo- → 4-((1-(4-fluorophenyl)-1H-indazol-5-yl)(hydroxy)methyl)benzonitrile

https://huagongshe.com/reaction/563431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrile, 4-bromo-HCID 12162—
Reactant1-(4-fluorophenyl)-1H-indazole-5-carbaldehydeHCID 57943612—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-((1-(4-fluorophenyl)-1H-indazol-5-yl)(hydroxy)methyl)benzonitrileHCID 6700551152.4%

Reaction Steps

To solution of 4-bromobenzonitrile (182 mg, 1.0 mmol) in 5 mL of dry THF at −78° C. was added n-BuLi (0.7 mL of 1.6 M hexanes solution, 1.1 mmol). The reaction was stirred 30 min and then 1-(4-fluorophenyl)-1H-indazol-5-carboxaldehyde (240 mg, 1.0 mmol) was added and the reaction mixture was allowed to warm to RT. After 12 h, quenched with brine and extracted 2×EtOAc. The organic layers were dried over MgSO4, filtered, and concentrated. The residue was purified on SiO2 by MPLC eluting with a 0-30% EtOAc/hexane gradient to give 180 mg (52% yield) of 4-((1-(4-fluorophenyl)-1H-indazol-5-yl)(hydroxy)methyl)benzonitrile. MS found: (M+H)+=344.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067447B2
Source datasetuspto-grants-2011_11
ORD IDord-6f8afc6a3f954ae0a09056ee7b16967a
Source noteuspto-grants-2011_11