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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239297Generated: November 2, 2026

Dimethylamine tetrahydrofuran → 4-(Benzyloxy)-N,N,2-trimethyl-1-tosyl-1H-benzo[d]imidazole-6-carboxamide

https://huagongshe.com/reaction/2239297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine tetrahydrofuranHCID 22320367—
ReactantHCID 67219535HCID 67219535—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product4-(Benzyloxy)-N,N,2-trimethyl-1-tosyl-1H-benzo[d]imidazole-6-carboxamideHCID 6722017442%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 6-bromo-2-methyl-1-[(4-methylphenyl)sulfonyl]-4-[(phenylmethyl)oxy]-1H-benzimidazole (53.0 g, 112 mmol, STEP 2) and tetrakis(triphenylphosphine)palladium(0) (25.9 g, 22.4 mmol) in 2M dimethylamine tetrahydrofuran solution (580 mL) was stirred at 65° C. under carbon mono-oxide gas (1 atmosphere) for 32 hours. The mixture was cooled to room temperature, and diluted with ethyl acetate (600 mL). The organic mixture was washed with saturated ammonium chloride aqueous solution (800 mL) and brine (500 mL), dried over magnesium sulfate and concentrated in vacuum. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate gradient elution from 1:2 to 1:3) to afford the title compound as a white solid (21.8 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723321B2
Source datasetuspto-grants-2010_05
ORD IDord-6d5cb90a823b4ba69bc72c8abc6d4df6
Source noteuspto-grants-2010_05