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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218135Generated: October 30, 2026

Hydrochloric Acid → 2-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2-phenylcyclopropanecarbonitrile

https://huagongshe.com/reaction/218135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcrylonitrileHCID 7855—
ReactantSodium HydroxideHCID 14798—
ReactantN'-((1-(4-fluorophenyl)-1H-indazol-5-yl)(phenyl)methylene)-4-methylbenzenesulfonohydrazideHCID 86640188—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
Product2-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2-phenylcyclopropanecarbonitrileHCID 5925109521%

Reaction Steps

(c)(d) N′-((1-(4-fluorophenyl)-1H-indazol-5-yl)(phenyl)methylene)-4-methylbenzenesulfonohydrazide (1.82 g, 3.77 mmol) was dissolved in 20 mL of dioxane and 20 mL of a 50% aqueous NaOH solution and heated at 85 C. After 1 h, the reaction mixture was adjusted to pH 4-5 with conc HCl and extracted 2× EtOAc. The organic layers were dried over MgSO4, filtered, concentrated, and the crude product was taken to the next step. Crude residue was dissolved in 20 mL of benzene and acrylonitrile (4 mmol) was added. The reaction mixture was heated to reflux. After 2 h, the reaction was poured into brine and extracted 2× EtOAc. The organic layers were dried over MgSO4, filtered, concentrated, and then purified by HPLC to give 275 mg (21% yield) of 2-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2-phenylcyclopropanecarbonitrile. MS found: (M+H)+=354.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198311B2
Source datasetuspto-grants-2012_06
ORD IDord-08bd22541c014e59b08c2ff509e6d74a
Source noteuspto-grants-2012_06