Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | HCID 86628635 | HCID 86628635 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | HCID 25216554 | HCID 25216554 | — |
Reaction Steps
To a N2 flushed vial was sequentially added trifluoromethanesulfonic acid 3-[4-(4-methyl-piperazin-1-yl)-pyridin-2-yl]-phenyl ester (20 mg, 0.05 mmol), Pd(PPh3)4 (10 mg), and toluene/EtOH (4:1, 1 mL). After 5 min, 4-fluorophenylboronic acid (10 mg, 0.07 mmol) and 2 M aqueous K2CO3 (0.2 mL) were added. The resulting mixture was heated at 90° C. for 16 h, then was poured into water and extracted with CH2Cl2. The organic layer was dried and concentrated, and the resulting residue was purified by preparative TLC (MeOH/CH2Cl2) to yield the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022209B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-82c0f97a9a024d3984cda4fc7b4ee291 |
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| Source note | uspto-grants-2011_09 |
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