HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Ethylpiperazin-1-yl)-3-(4-methoxyphenyl)isoquinoline → 1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Ethylpiperazin-1-yl)-3-(4-methoxyphenyl)isoquinoline | HCID 9950168 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | 1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinoline | HCID 135719042 | 75% |
Reaction Steps
1-(4-Ethylpiperazin-1-yl)-3-(4-methoxyphenyl)isoquinoline (1.50 g) obtained in Example 10 was dissolved in 48% hydrobromic acid (15 ml) and reacted at 120° C. for 1.5 hr. The reaction solution was evaporated to a final half volume, and ice-cooled. The resulting precipitates were collected by filtration, and then washed with a small amount of ice-cold water. The precipitates were treated with a 2N aqueous solution of sodium hydroxide, followed by collecting the precipitates by filtration, washed with water and ether/n-hexane, and then dried in warm air, to give the title compound (1.08 g, yield; 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790844B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-b0fba5fc8464411eb0c6fb7f53a15b8b |
| Source note | uspto-grants-2004_09 |