HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693097Generated: November 1, 2026
(Pyridin-4-yl)boronic acid → 5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-pyridin-4-yl-2-trifluoromethyl-phenyl)-amide
https://huagongshe.com/reaction/1693097
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | 5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-bromo-2-trifluoromethyl-phenyl)-amide | HCID 24965274 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-pyridin-4-yl-2-trifluoromethyl-phenyl)-amide | HCID 24965623 | 70.3% |
Reaction Steps
A suspension of 5-fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-bromo-2-trifluoromethyl-phenyl)-amide (0.5 g) and 4-pyridineboronic acid (0.197 g) in 1,2-dimethoxyethane (6 ml), ethanol (2 ml) and 2 M aqueous sodium carbonate solution (4.0 ml) was degassed 3-4 times to remove oxygen, then tetrakis(triphenylphosphine)palladium (0.065 g) was added. The reaction mixture was stirred at 80° C. for 3 h, quenched with ice/water, and extracted with ethyl acetate. The organic layers were washed, dried and concentrated. The residue was chromatographed over silica gel using heptane/ethyl acetate as eluent to obtain the title compound (0.35 g) as a yellowish solid. MS (ISP): 467.3 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158655B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-24ac4c2bd64d48e18134f96aba296de2 |
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| Source note | uspto-grants-2012_04 |
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