HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Xylyl bromide → N,N-diethyl-4-[[4-(4-methylbenzyl)-1-piperazinyl](8-quinolinyl)methyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,N-diethyl-4-(1-piperazinyl(8-quinolinyl)methyl)benzamide | HCID 9801260 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N,N-diethyl-4-[[4-(4-methylbenzyl)-1-piperazinyl](8-quinolinyl)methyl]benzamide | HCID 10185707 | — |
Reaction Steps
To a solution of compound 1 (0.80 g; 1.99 mmol) in CH2Cl2 (20 ml) was added Et3N (0.83 ml; 5.97 mmol) followed by p-methyl benzyl bromide (773 mg; 4.18 mmol). The reaction mixture was stirred overnight and was then was concentrated under reduced pressure. Purification by reverse phase using 10%-30% CH3CN/H2O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06784181B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-66b7398f7eee44fdb49a148db594eb7b |
| Source note | uspto-grants-2004_08 |