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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504227Generated: October 29, 2026

(Chloromethyl)dimethylisopropoxysilane → 1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-(isopropoxy-dimethyl-silanyl)-ethanol

https://huagongshe.com/reaction/504227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Chloromethyl)dimethylisopropoxysilaneHCID 266137—
Reactant6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazole-5-carbaldehydeHCID 11245608—
SolventTetrahydrofuranHCID 8028—
Product1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-(isopropoxy-dimethyl-silanyl)-ethanolHCID 21114167—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of the Grignard reagent prepared from Mg and chloromethyl dimethylisopropoxy silane (Org. Synth. 1992, 69, 96) [4.4 mL, 3.26 mmol, 0.74 M solution (based on 90% purity)] in THF, is added a solution of 6-(4-bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazole-5-carbaldehyde 10f (200 mg, 0.54 mmol) in THF (1 mL) at −78° C. After stirring for 1 hour at −78° C., the reaction is quenched with saturated aqueous NH4Cl, and extracted with EtOAc. The organic layer is dried over MgSO4, filtered, concentrated in vacuo to afford the crude desired product which is directly used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777050B2
Source datasetuspto-grants-2010_08
ORD IDord-ccd9c5b4485a4ac4b78b26e5549d549e
Source noteuspto-grants-2010_08