HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007014Generated: October 28, 2026
1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 178462710, compound
https://huagongshe.com/reaction/1007014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline | HCID 22502447 | — |
| Reactant | HCID 178448214 | HCID 178448214 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178462710 | HCID 178462710 | 87.1% |
Reaction Steps
Trans-4-(tributylstannylphenyl)cyclohexyl acetate(0.56 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.46 g) -were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.06 g) in xylene in nitrogen atmosphere overnight. After cooling, the reaction solution was diluted with ethyl acetate and filtered. The filtrate was extracted with 2N hydrochloric acid, and the resulting aqueous layer was washed with ethyl acetate. Then, it was adjusted to pH 10 by a 8N aqueous solution of sodium hydroxide, extracted with ethyl acetate, washed with a 10% aqueous solution of sodium carbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give a mixture (0.44 g) of 1-(4-ethylpiperazin-1-yl)-3-[4-(trans-4-acetoxycyclohexyl)phenyl]isoquinoline as a brown viscous oil and the starting material.
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-c9c8c65be7864034be8acb2c7b20c05e |
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| Source note | uspto-grants-2004_09 |
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