HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-2-(chloromethyl)-1-methoxybenzene | HCID 10354068 | — |
| Reactant | 2-Piperazinylpyrimidine dihydrochloride | HCID 11680272 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidine | HCID 1240303 | 235% |
Reaction Steps
A mixture of 1.1 g of 2-(chloromethyl)-4-bromoanisole, 1 g of 1-(2-pyrimidyl)piperazine dihydrochloride and 2.0 mL N,N-diisopropylethylamine in 10 mL chloroform was heated at reflux temperature for 2 hr, cooled to room temperature, washed with 1 N NaOH and water. The solvent was removed by evaporation under reduced pressure to yield 3.6 g of 2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]-4-bromoanisole as a white solid which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06221871B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-a6541a6b4c3c406ba75045da9a273aa6 |
| Source note | uspto-grants-2001_04 |