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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50909Generated: October 29, 2026

N1-(pyridin-2-yl)benzene-1,2-diamine → (E)-1-(2-Pyridyl)-2-[2-(2-thienyl)ethenyl]-1H-benzimidazole

https://huagongshe.com/reaction/50909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN1-(pyridin-2-yl)benzene-1,2-diamineHCID 752150—
Reactant(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
Reactant3-(2-Thienyl)acryloyl chlorideHCID 11263780—
Product(E)-1-(2-Pyridyl)-2-[2-(2-thienyl)ethenyl]-1H-benzimidazoleHCID 9839419—

Reaction Steps

The tilled compound was prepared from N-(2-pyridyl)-o-phenylenediamine and (E)-3-(2-thienyl)acryloyl chloride (Aitken, R. A.; Boeters, C.; Morrison, J. J. J. Chem. Soc. Perkin. Trans. 1, 1994, 17, 2473) according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). MW: 303.39; mp: 130.0-131.0° C.; 1H-NMR (CDCl3) δ: 8.77 (1H, ddd, J=4.8, 1.8, 0.7 Hz), 8.12 (1H, d, J=15.8 Hz), 8.02 (1H, ddd, J=8.1,8.1, 1.8 Hz), 7.84-7.79 (1H, m), 7.51 (1H, ddd, J=8.1, 1.1, 0.7 Hz), 7.49-7.43 (2H, m), 7.37-7.18 (3H, m), 7.20 (1H, dd, J=3.7,0.7 Hz), 7.02 (1H, dd, J=4.8, 3.7 Hz), 6.94 (1H, d, J=15.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713482B2
Source datasetuspto-grants-2004_03
ORD IDord-36d30027d4d04e029bff37f9b0e8492e
Source noteuspto-grants-2004_03