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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50943Generated: October 27, 2026

(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole → (E)-5-Fluoro-2-[2-(3-furyl)ethenyl]-1-(2-pyridyl)-1H-benzimidazole

https://huagongshe.com/reaction/50943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
Reactant4-fluoro-2-amino-N-(2-pyridyl)anilineHCID 22736745—
Reactant3-Cyclohexylprop-2-enoyl chlorideHCID 56623207—
Product(E)-5-Fluoro-2-[2-(3-furyl)ethenyl]-1-(2-pyridyl)-1H-benzimidazoleHCID 22736678—

Reaction Steps

The titled compound was prepared from 4-fluoro-2-amino-N-(2-pyridyl)aniline and (E)-3-(3-Cyclohexylacryloyl chloride according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). MW: 305.31; mp: 168.0-170.0° C.; 1H-NMR (CDCl3) δ: 8.82-8.76 (1H, m), 8.15 (1H, d, J=16.0 Hz), 8.04 (1H, ddd, J=7.7, 7.7, 1.8 Hz), 7.71 (1H, s), 7.60-7.50 (3H, m), 7.43-7.33 (2H, m), 7.05 (1H, ddd, J=9.1, 9.1, 2.5 Hz), 6.74 (1H, d, J=16.0 Hz), 6.53 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713482B2
Source datasetuspto-grants-2004_03
ORD IDord-74bf31554aca427f83f8aeec0e68dc79
Source noteuspto-grants-2004_03