HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617454Generated: November 4, 2026
Triphenylphosphine → HCID 136166843, compound
https://huagongshe.com/reaction/1617454
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | (Pyrimidin-5-yl)boronic acid | HCID 2795193 | — |
| Reactant | HCID 136167080 | HCID 136167080 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | N,N-Dimethylacetamide--water (1/1) | HCID 21534740 | — |
| Product | HCID 136166843 | HCID 136166843 | 451% |
Reaction Steps
To a stirred solution of (E)-3-(4-bromo-phenyl)-3-phenyl-1-pyridin-4-yl-propan-1-one oxime (example 5, 10 mg) and pyrimidine-5-boronic acid (49 mg) in a mixture of DMA/H2O (2.1 mL, 20:1) tetrakis(triphenylphosphine)palladium (0) (36 mg), triphenylphosphine (17 mg) and potassium fluoride (31 mg) were added. The mixture was irradiated in the microwave at 140° C. for 15 min. A saturated aqueous solution of NH4Cl was added, the phases were separated and the inorganic one was extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash chromatography on an ISOLUTE Flash NH2 cartridge (EtOAc) to yield the title compound (45 mg, 45%) as a white foam, MS (ESI+): m/z=381.1 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08765730B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-8723b02b9efa436390a89b4f5debc9fb |
|---|
| Source note | uspto-grants-2014_07 |
|---|