Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | p-Chlorophenylboric acid | HCID 17810664 | — |
| Reactant | HCID 59759140 | HCID 59759140 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59759137 | HCID 59759137 | 90.9% |
Reaction Steps
Under nitrogen atmosphere, 2-[(4-{2-[(5-bromopyrazin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl ester (10.5 g) synthesized in Example 226-1 and 4-chlorophenylboric acid (5.36 g) were dissolved in dioxane (80 mL) and aqueous sodium carbonate solution (2 mol/L, 40 mL), tetrakis(triphenylphosphine)palladium (1.32 g) was added, and the mixture was refluxed for 4 hr. The reaction mixture was cooled, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate=2:1) to give the title compound (10.2 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08026370B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-58f8483c32394396907667008f0d6bea |
|---|
| Source note | uspto-grants-2011_09 |
|---|