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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50919Generated: October 26, 2026

4-Methyl-2-nitroaniline → (E)-5-Methyl-1-(2-pyridyl)-2-styryl-1H-benzimidazole

https://huagongshe.com/reaction/50919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-2-nitroanilineHCID 6978—
Reactant(E)-1-(2-pyridyl)-2-styryl-5-trifluoromethyl-1H-benzimidazoleHCID 22736704—
Product(E)-5-Methyl-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 22736726—

Reaction Steps

The titled compound was prepared from 4-methyl-2-nitroaniline according to the preparation of (E)-1-(2-pyridyl)-2-styryl-5-trifluoromethyl-1H-benzimidazole (Example 57). MW: 311.39; mp: 144.8-146.0° C.; 1H-NMR (CDCl3) δ: 8.77-8.72 (1H, m), 7.99-7.91 (1H, m), 7.98 (1H, d, J=16.1 Hz), 7.61 (1H, s), 7.53-7.26 (8H, m), 7.15 (1H, d, J=16.1 Hz), 7.10-7.05 (1H, m), 2.50 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713482B2
Source datasetuspto-grants-2004_03
ORD IDord-ec07f6fcec914c4aa0efed64a89c6c4c
Source noteuspto-grants-2004_03