HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Pyridinylboronic acid → 5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-pyridin-3-yl-2-trifluoromethyl-phenyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | 5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-bromo-2-trifluoromethyl-phenyl)-amide | HCID 24965274 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| 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-3-yl-2-trifluoromethyl-phenyl)-amide | HCID 24965627 | 86.3% |
Reaction Steps
This compound was prepared in analogy to Example 2 starting from 5-fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid(4-bromo-2-trifluoromethyl-phenyl)-amide (0.10 g) and 3-pyridineboronic acid (0.052 g) in 1,2-dimethoxyethane (1.5 ml), ethanol (0.32 ml) and 2 M aqueous sodium carbonate solution (0.8 ml) with tetrakis(triphenylphosphine)palladium (0.050 g) to obtain the title compound (0.086 g) as a colorless solid. MS (ISP): 467.0 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158655B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-b228778651044c5cb3598c54e22f8795 |
| Source note | uspto-grants-2012_04 |