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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659696Generated: October 29, 2026

Sodium Carbonate → 3-[3-(2-Imidazol-1-ylacetyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide

https://huagongshe.com/reaction/659696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(2-(N-(tert-Butyl)sulfamoyl)-5-isobutylthiophen-3-yl)boronic acidHCID 11484000—
Reactant1-(3-Bromophenyl)-2-imidazol-1-ylethanoneHCID 43797856—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-[3-(2-Imidazol-1-ylacetyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamideHCID 6713295495%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-(3-bromophenyl)-2-imidazol-1-ylethanone (102 mg, 0.385 mmol; see step (a)) in toluene (10 mL) and ethanol (1 mL) was added 5-isobutyl-2-(N-tert-butylaminosulfonyl)thiophene-3-boronic acid (209 mg, 0.654 mmol; see Example 1(c)), Pd(PPh3)4 (26.7 mg, 0.023 mmol) and Na2CO3 (769 μL, 1.54 mmol, 2.0 M aq), and the reaction mixture was stirred for 4 h at 80° C. The reaction mixture was diluted with water (10 mL) and extracted with EtOAc. The combined organic phase was dried (over anhydrous MgSO4), concentrated in vacuo, and the residue was purified by flash chromatography using MeOH:CH2Cl2 (6:94) as eluent to give the sub-title compound as a colourless syrup in 95% yield (168 mg, 0.366 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080571B2
Source datasetuspto-grants-2011_12
ORD IDord-7bdfe7d756da44f8a2385d6132dd2bee
Source noteuspto-grants-2011_12