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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554195Generated: October 26, 2026

Sodium Carbonate → tert-Butyl methyl{[1-(phenylsulfonyl)-5-(3-thienyl)-1H-pyrrol-3-yl]methyl}carbamate

https://huagongshe.com/reaction/554195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium BicarbonateHCID 516892—
ReactantThiophene-3-boronic acidHCID 581760—
Reactanttert-butyl{[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 66924909—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Producttert-Butyl methyl{[1-(phenylsulfonyl)-5-(3-thienyl)-1H-pyrrol-3-yl]methyl}carbamateHCID 6692493588%

Reaction Conditions

Temperature105 °C

Reaction Steps

A suspension of tert-butyl {[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate (1.02 g), 3-thienylboronic acid (0.61 g), tetrakis(triphenylphosphine)palladium (0.41 g) and sodium carbonate (0.75 g) in 1,2-dimethoxyethane (25 mL)-water (25 mL) was stirred at 105° C. for 7 hr. After cooling, saturated aqueous sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate, water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1) to give the title compound as a colorless solid (yield 0.90 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-47b51d45e7a94c15a37ec68dff8ba9f8
Source noteuspto-grants-2011_11