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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077805Generated: November 4, 2026

Water → N-{[(2-{4-[2-ethyl-5-(1-hydroxy-1-methylethyl)-1H-benzimidazol-1-yl]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide

https://huagongshe.com/reaction/2077805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 21875662HCID 21875662—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
ProductN-{[(2-{4-[2-ethyl-5-(1-hydroxy-1-methylethyl)-1H-benzimidazol-1-yl]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamideHCID 11720560101.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of N-[({2-[4-(5-acetyl-2-ethyl-1H -benzimidazol-1-yl)phenyl]ethyl}amino)carbonyl]-4-methylbenzenesulfonamide (Example 78, 100 mg, 0.19 mmol) in tetrahydrofurane (15 ml) was added MeMgI (1.2 ml, 0.99 mmol) dropwise under nitrogen at 0° C. The mixture was stirred at 0° C. for 1 h and then was stirred at rt for 30 min. The mixture was added water (10 ml) and extracted with CH2Cl2(50 ml). The organic layer was washed with brine (10 ml), then dried (Na2SO4). After removal of solvent, the crude product was purified by flash column chromatography eluting with CH2Cl2:methanol (30:1/20:1/10:1) to afford 100 mg (97%) of the title compound as white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928119B2
Source datasetuspto-grants-2011_04
ORD IDord-9404a593182f4557aacfafa717011f59
Source noteuspto-grants-2011_04