HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Bromoacetophenone → HCID 9797677, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-(1-Methylpiperidin-4-yl)-1H-Indole-5-Boronic Acid | HCID 12041813 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 9797677 | HCID 9797677 | 70% |
Reaction Steps
The title compound was prepared by the procedure of Example 10, beginning with 3-(1-methylpiperidin-4-yl)-1H-indole-5-boronic acid (0.200 g, 0.77 mmol), 1-bromo-4-acetylbenzene (0.147 g, 0.74 mmol), tetrakis(triphenylphosphine)palladium(O) (0.045 g, 0.039 mmol), and 2M aqueous sodium carbonate solution (2 mL) in 15 mL of tetrahydrofuran:methanol (1:1) to give the title compound (0.171 g, 70%) as an amorphous solid. FDMS m/e=348 (M+). EA calculated for C22H24N2O.¼ H2O: C, 78.19; H, 7.31; N, 8.29. Found: C, 78.00; H, 7.27; N, 7.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358972B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-00130e22f3d44fe3a05bafc9acc589cc |
| Source note | uspto-grants-2002_03 |