HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006977Generated: October 30, 2026
1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22503411, compound
https://huagongshe.com/reaction/1006977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline | HCID 22502447 | — |
| Reactant | HCID 22503540 | HCID 22503540 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22503411 | HCID 22503411 | 22.5% |
Reaction Steps
N-(2-Benzyloxyethyl)-4-tributylstannylbenzamide (1.23 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.49 g) were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.13 g) in xylene in nitrogen atmosphere for 3 hr. After cooling, the reaction solution was filtered and concentrated. The resulting residue was purified by silica gel column chromatography (chloroform/methanol system). The resulting product was dissolved in ethyl acetate and extracted with 2N hydrochloric acid. The aqueous layer was washed with ethyl acetate, adjusted to pH 10 with a 8N aqueous solution of sodium hydroxide, and then extracted with ethyl acetate. The extract was washed with a 10% aqueous solution of sodium carbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give 1-(4-ethylpiperazin-1-yl)-3-{4-[N-(2-benzyloxyethyl)carbamoyl]phenyl}isoquinoline (0.17 g) as a pale brown viscous 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-610755ac53dc40228b09f3a96e96eb95 |
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| Source note | uspto-grants-2004_09 |
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