Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 57417713 | HCID 57417713 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57417712 | HCID 57417712 | 45% |
Reaction Steps
In 3 mL of THF, 68 mg of imidazole and 152 mg of DBU were dissolved, into which 155 mg of phenylacetyl chloride was dropped under cooling with ice and stirring, followed by 1.5 hours' stirring at room temperature. Then a solution of 137 mg of 5-amino-3-(2,3-difluorophenyl)-4-(4-pyridyl)isoxazole and 152 mg of DBU in 3 mL of THF was added dropwise, followed by 26 hours' stirring at room temperature. After addition of water, the reaction solution was extracted with ethyl acetate. The ethyl acetate extract was washed first with saturated aqueous NaHCO3 solution and then with brine, dried over anhydrous magnesium sulfate, and removed of the solvent by reduced pressure distillation. The resultant residue was purified by thin-layer silica gel chromatography (developer, hexane:ethyl acetate=1:1) to provide 88 mg (yield: 45%) of the title compound as colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08207203B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-f71f985a88724cb2aa8704667fc536e0 |
|---|
| Source note | uspto-grants-2012_06 |
|---|