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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967827Generated: October 25, 2026

p-Cyanobenzenesulphonamide → 4-cyano-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamide

https://huagongshe.com/reaction/967827

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-CyanobenzenesulphonamideHCID 76566—
Reactant2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamateHCID 22291350—
Product4-cyano-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamideHCID 22291395—

Reaction Steps

The title compound was prepared according to the procedure described in step 2 of Example 18 from 2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamate and 4-cyanobenzenesulfonamide. MS (ESI) m/z 500 [M+H]+, 498 [M−H]−, 1H-NMR (DMSO-d6) δ 1.14 (3H, t, J=7.5 Hz), 2.61 (2H, q, J=7.5 Hz), 2.72 (2H, t, J=7.1 Hz), 3.10-3.30 (2H, m), 6.60 (1H, br), 7.19 (1H, t, J=7.1 Hz), 7.28-7.39 (6H, m), 7.70 (1H, s), 7.78 (2H, d, J=7.1 Hz), 8.00-8.08 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956050B2
Source datasetuspto-grants-2005_10
ORD IDord-b80c72395def4bf9869ba13d178ca21e
Source noteuspto-grants-2005_10