HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560119Generated: October 26, 2026
Water → 4-Benzenesulfonyl-6-(3'-methanesulfonyl-biphenyl-3-yl)-1-phenyl-piperazin-2-one
https://huagongshe.com/reaction/560119
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Methylsulfonyl)phenylboronic acid | HCID 2773542 | — |
| Reactant | 4-Benzenesulfonyl-6-(3-bromo-phenyl)-1-phenyl-piperazin-2-one | HCID 67000436 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Benzenesulfonyl-6-(3'-methanesulfonyl-biphenyl-3-yl)-1-phenyl-piperazin-2-one | HCID 44548559 | 50% |
Reaction Steps
To a solution of 4-benzenesulfonyl-6-(3-bromo-phenyl)-1-phenyl-piperazin-2-one (100 mg), (3-methylsulfonylphenyl) boronic acid (46.7 mg) and tetrakis(triphenylphosphine)palladium(0) (24.5 mg) in 1,2-dimethoxyethane (2mL) was added potassium carbonate (73.3 mg). The reaction mixture was stirred at 80° C. overnight. Additional amounts of (3-methylsulfonylphenyl) boronic acid (21 mg), potassium carbonate (58.6 mg) and tetrakis(triphenylphosphine)palladium(0) (24.5 mg) were added and stirring was continued at 80° C. for 3 h. To the reaction mixture water and ethyl acetate were added, the phases were separated, and the inorganic one was extracted with ethyl acetate (×2). The organic layers were combined, washed with brine, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography (SiO2, n-heptane/ethyl acetate 1:3, followed by ISOLUTE Flash NH2, n-heptane/ethyl acetate 1:1) to yield 58 mg (50%) of 4-benzenesulfonyl-6-(3′-methanesulfonyl-biphenyl-3-yl)-1-phenyl-piperazin-2-one as a white foam, MS: 547.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063088B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b34ce2a156ba4ec9bc8548d1ddbc5a37 |
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| Source note | uspto-grants-2011_11 |
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