Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413419Generated: October 30, 2026

N-[(4-cyano-3-fluoro-phenyl)-(3-methyl-3H-imidazol-4-yl)-methylene]-2-methylpropanesulfinamide → N-[1-(4-cyano-3-fluoro-phenyl)-1-(3-methyl-3H-imidazol-4-yl)-ethyl]-2-methylpropanesulfinamide

https://huagongshe.com/reaction/413419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[(4-cyano-3-fluoro-phenyl)-(3-methyl-3H-imidazol-4-yl)-methylene]-2-methylpropanesulfinamideHCID 86584782—
ReactantHCID 178418689HCID 178418689—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-[1-(4-cyano-3-fluoro-phenyl)-1-(3-methyl-3H-imidazol-4-yl)-ethyl]-2-methylpropanesulfinamideHCID 18533209—

Reaction Steps

N-[(4-Cyano-3-fluoro-phenyl)-(3-methyl-3H-imidazol-4-yl)-methylene]-2-methylpropanesulfinamide (1.50 g, 4.51 mmol) was dissolved in anhydrous THF (30 mL) at 0° C. and treated with a 3.0M solution of MeMgBr (4.50 mL, 13.5 mmol) in Et2O. After 15 min the reaction was quenched with aq. NH4Cl solution, diluted with saturated NaHCO3 solution and extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), filtered, concentrated, and recrystallized from 95% EtOAc/Hexane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566385B2
Source datasetuspto-grants-2003_05
ORD IDord-c4951cdf9ea64dc4ad51c9d7d3c64a88
Source noteuspto-grants-2003_05