HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 10618874, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[3-(4-Chlorophenyl)-1H-pyrazol-5-yl]piperidine | HCID 449126 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10618874 | HCID 10618874 | — |
Reaction Steps
To a solution of 4-[3-(4-chlorophenyl)-1H-pyrazol-5-yl]piperidine (INTERMEDIATE 7, 4 g, 15.28 mmol) in 60 mL DMF was added K2CO3 (63 g, 45.8 mmol), and 2-(bromoethyl)benzene (2.3 mL, 16.8 mmol). The reaction mixture was stirred at ambient temperature overnight, diluted with EtOAc, and washed three times with water. The organic layer was separated, dried (MgSO4), and concentrated under reduced pressure. LC-MS m/z=366.17 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365539B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-1611d3c8b3a147a3a4cc38eadca9dfc5 |
| Source note | uspto-grants-2016_06 |