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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340767Generated: October 30, 2026

Diisopropylethylamine → 5-biphenyl-4-yl-6-chloro-2-(methylsulfonyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazole

https://huagongshe.com/reaction/340767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant5-biphenyl-4-yl-6-chloro-2-(methylsulfonyl)-1H-benzimidazoleHCID 68486886—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-biphenyl-4-yl-6-chloro-2-(methylsulfonyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazoleHCID 58387130—

Reaction Steps

To a solution of 5-biphenyl-4-yl-6-chloro-2-(methylsulfonyl)-1H-benzimidazole (5.37 g, 14.0 mmol) in THF (70 mL) was added DIPEA (3.67 mL, 21.0 mmol) followed by SEMCl (3.7 mL, 21.0 mmol). The reaction was maintained for 5 h at ambient temperature. Then the reaction mixture was diluted with EtOAc and washed with saturated aqueous NaHCO3, followed by brine. The organic phase was dried over Na2SO4, filtered, and concentrated. Chromatography of the resulting residue over silica eluting with 5-25% EtOAc/hexanes afforded the desired product as a white solid. LC-MS: calculated for C14H20ClN2O3SSi 485.97, observed m/e 428.83 (M+H)+ (Rt 2.30 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895596B2
Source datasetuspto-grants-2014_11
ORD IDord-6238e7b8a5e4458f9a7b58f8f0b4211d
Source noteuspto-grants-2014_11