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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | tert-butyl{[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate | HCID 66924909 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | tert-Butyl methyl{[1-(phenylsulfonyl)-5-(3-thienyl)-1H-pyrrol-3-yl]methyl}carbamate | HCID 66924935 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048909B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-47b51d45e7a94c15a37ec68dff8ba9f8 |
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| Source note | uspto-grants-2011_11 |
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