HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 42645471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-chloro-4-(piperazin-1-yl)phenyl)picolinamide | HCID 67441344 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 42645471 | HCID 42645471 | 192.2% |
Reaction Steps
According to Scheme 5 Step 5 Method B: A suspension of (bromomethyl)benzene (0.61 mmol, 74 μL), N-(3-chloro-4-(piperazin-1-yl)phenyl)picolinamide (0.51 mmol, 161 mg) and of K2CO3 (0.51 mmol, 70 mg) in ACN (3 mL) was stirred at 80° C. for 30 minutes. After evaporation of the solvent, water and AcOEt were added. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over silica gel using DCM/AcOEt (80:20) as eluent and finally crystallized in pentane to obtain N-(4-(4-benzylpiperazin-1-yl)-3-chlorophenyl)picolinamide (0.98 mmol, 40 mg, 20%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524726B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-ffabc75a608944ac845f7dfd6409fe52 |
| Source note | uspto-grants-2013_09 |