HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22502713, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline | HCID 22502447 | — |
| Reactant | HCID 178467830 | HCID 178467830 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22502713 | HCID 22502713 | 59.5% |
Reaction Steps
To a mixture solution of 1-(4-ethylpiperazin-1-yl)-3-bromoisoquinoline (0.71 g) cooled to 0° C. and [1,3-bis(diphenylphosphino)propane]dichloronickel(II) (0.05 g) in diethyl ether (20 ml) was dropwise added 1M benzylmagnesium chloride/ether solution (4.5 ml) in nitrogen atmosphere. The reaction mixture was stirred at room temperature overnight. The reaction solution was diluted with ether (30 ml), washed with water and brine, and then dried over magnesium sulfate. The solvent was removed, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/acetone system), to give the title compound (0.44 g; 59.5%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06340759B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-21c92eb7b9924b16bcc993ecf304f125 |
| Source note | uspto-grants-2002_01 |