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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227163Generated: November 1, 2026

Potassium Carbonate → [(S)-1-(6-ethynyl-1H-benzoimidazol-2-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/227163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant[(S)-2-phenyl-1-(6-trimethylsilanylethynyl-1H-benzoimidazol-2-yl)-ethyl]-carbamic acid tert-butyl esterHCID 66815258—
SolventMethanolHCID 887—
Product[(S)-1-(6-ethynyl-1H-benzoimidazol-2-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl esterHCID 8662792372%

Reaction Steps

To a solution of [(S)-2-Phenyl-1-(6-trimethylsilanylethynyl-1H-benzoimidazol-2-yl)-ethyl]-carbamic acid tert-butyl ester (90 mg, 0.208 mmol) in methanol (10 mL) at room temperature, was added finely powdered anhydrous potassium carbonate (258 mg, 1.87 mmol). The resulting heterogenous mixture was stirred at room temperature until LC/MS indicated the reaction was complete. The solvent was then allowed to evaporate and resulting residue was partitioned in 1:1 v/v water/ethyl acetate (50 mL total volume) and the aqueous layer was separated and extracted twice with ethyl acetate (20 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The yellowish colored residue was applied to a silica gel column using dichloromethane (10 mL) and gradient eluted from 10 to 75% v/v ethyl acetate in hexanes to give [(S)-1-(6-ethynyl-1H-benzoimidazol-2-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester (54 mg, 72%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557221B2
Source datasetuspto-grants-2009_07
ORD IDord-7b84682a75da435cb689e4cef660c4b6
Source noteuspto-grants-2009_07