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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060896Generated: October 31, 2026

Triethylamine → N-{3-[1-(4-Cyano-3-fluoro-phenyl)-1-(3-methyl-3H-imidazol-4-yl)-ethylamino]-propyl}-3-hydroxy-benzenesulfonamide

https://huagongshe.com/reaction/1060896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(+)-4-[1-amino-1-(3-methyl-3H-imidazol-4-yl)-ethyl]-2-fluoro-benzonitrileHCID 11470581—
ReactantN-(3-bromo-propyl)-3-hydroxy-benzenesulfonamideHCID 18629458—
SolventAcetonitrileHCID 6342—
ProductN-{3-[1-(4-Cyano-3-fluoro-phenyl)-1-(3-methyl-3H-imidazol-4-yl)-ethylamino]-propyl}-3-hydroxy-benzenesulfonamideHCID 70026827—

Reaction Steps

N-(3-Bromo-propyl)-3-hydroxy-benzenesulfonamide (0.23 g, 0.782 mmol), (+)-4-[1-amino-1-(3-methyl-3H-imidazol-4-yl)-ethyl]-2-fluoro-benzonitrile (Example 1, Step I) (0.191 g, 0.78 mmol), and Et3N (0.218 mL, 1.56 mmol) were dissolved in CH3CN (5 mL) and heated at reflux for 16 h. The reaction mixture was concentrated in vacuo, azeotroped with toluene, and dried to give the title compound. MS (M+1) 458.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525074B2
Source datasetuspto-grants-2003_02
ORD IDord-57d6f351b74f419ca0157b8ec036bd8f
Source noteuspto-grants-2003_02