HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007027Generated: November 1, 2026
Water → 1-(4-Ethylpiperazin-1-yl)-3-phenacylisoquinoline
https://huagongshe.com/reaction/1007027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | 1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline | HCID 22502447 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Catalyst | Mercury | HCID 23931 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(4-Ethylpiperazin-1-yl)-3-phenacylisoquinoline | HCID 22503451 | 89.1% |
Reaction Steps
A mixed solution of 1-(4-ethylpiperazin-1-yl)-3-bromoisoquinoline (1.00 g), acetophenone (1.50 g) and tert-butoxypotassium (1.40 g) in dimethyl sulfoxide (50 ml) was irradiated with light (450 W; mercury-vapor lamp) at room temperature for 5 hr. Water (200 ml) was added to the reaction solution, and the mixture was extracted with ethyl acetate. The resulting organic layer was washed with water and brine, and then extracted with a 2N aqueous solution of hydrochloric acid (100 ml). The resulting aqueous layer was basified with sodium carbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine, and dried over magnesium sulfate. The solvent was removed, to give 1-(4-ethylpiperazin-1-yl)-3-phenacylisoquinoline (1.0 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790844B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-1c1471c6455c49889abd8320b8554c8d |
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| Source note | uspto-grants-2004_09 |
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