HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814556Generated: October 31, 2026
1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22503385, compound
https://huagongshe.com/reaction/1814556
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline | HCID 22502447 | — |
| Reactant | HCID 22503653 | HCID 22503653 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22503385 | HCID 22503385 | 46.7% |
Reaction Steps
N-Methyl-N-(2-benzyloxyethyl)-4-tributylstannylbenzamide (1.93 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.93 g) were heated under reflux overnight in the presence of tetrakistriphenylphosphinepalladium(0) (0.13 g) in xylene in nitrogen atmosphere. After cooling, the reaction solution was diluted with ethyl acetate and filtered. The filtrate was extracted with 2N hydrochloric acid. The aqueous layer was washed with ethyl acetate and adjusted to pH 10 by a 8N aqueous solution of sodium hydroxide, which was then extracted with ethyl acetate, washed with a 10% aqueous solution of sodium carbonate and brine, and then dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol system), to give 1-(4-ethylpiperazin-1-yl)-3-{4-[N-(2-benzyloxyethyl)-N-methylcarbamoyl]phenyl}isoquinoline (0.69 g) as a pale yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875761B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-8c2c02cc7f1f48e6a54dcdb6f36cbece |
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| Source note | uspto-grants-2005_04 |
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