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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50908Generated: October 29, 2026

4-(2-Aminoanilino)pyridine → (E)-2-[2-(3-Furyl)ethenyl]-1-(4-pyridyl)-1H-benzimidazole

https://huagongshe.com/reaction/50908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Aminoanilino)pyridineHCID 291132—
Reactant(E)-1-(4-Pyridyl)-2-styryl-1H-benzimidazoleHCID 9948158—
Reactant(E)-3-(Furan-3-yl)acryloyl chlorideHCID 22736687—
Product(E)-2-[2-(3-Furyl)ethenyl]-1-(4-pyridyl)-1H-benzimidazoleHCID 22736738—

Reaction Steps

The titled compound was prepared from N-(4-pyridyl)-o-phenylenediamine and (E)-3-(3-furyl)acryloyl chloride according to the preparation of (E)-1-(4-pyridyl)-2-styryl-1H-benzimidazole (Example 3). MW: 287.32; mp: 171.5-172.5° C.; 1H-NMR (DMSO) δ: 8.88 (2H, dd, J=4.6, 1.7 Hz), 8.07 (1H, br.s), 7.81 (1H, d, J=15.8 Hz), 7.74-7.65 (4H, m), 7.35-7.25 (3H, m), 6.89 (1H, br.s), 6.73 (1H, d, J=15.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713482B2
Source datasetuspto-grants-2004_03
ORD IDord-f2a3f464c92a413f868c331fbf2f5be5
Source noteuspto-grants-2004_03