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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183145Generated: October 30, 2026

Quinoline → 5-[(1Z)-2-Phenylvinyl]-3-(4-fluorophenyl)-1H-indazole

https://huagongshe.com/reaction/2183145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
Reactant3-(4-Fluorophenyl)-5-(2-Phenylethynyl)-1H-IndazoleHCID 22480162—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-[(1Z)-2-Phenylvinyl]-3-(4-fluorophenyl)-1H-indazoleHCID 5744092046%

Reaction Steps

A mixture of 3-(4-fluorophenyl)-5-(2-phenylethynyl)-1H-indazole (0.050 g, 0.16 mmol), quinoline (0.030 g), and palladium (5 wt. % on barium carbonate, 0.015 g) in ethyl acetate (10 mL) was stirred under hydrogen for 5 hours. It was filtered with celite and washed with ethyl acetate. The filtrate was washed with 5% hydrochloric acid solution and brine, dried over magnesium sulfate, filtered, and concentrated. The residue was then purified by chromatography (SiO2, 15-30% ethyl acetate/hexane) and by HPLC to provide the title compound (0.023 g, 46% yield): 1H NMR (CDCl3) δ 10.15 (br s, 1H), 7.83 (s, 1H), 7.70 (m, 2H), 7.29 (m, 7H), 7.11 (t, 2H), 6.72 (d, 1H), 6.68 (d, 1H); ES-MS (m/z) 315 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-88ea7b01008b4e4eb7c8b214d3ceaf15
Source noteuspto-grants-2005_05