HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814531Generated: October 30, 2026
2-Methoxy-5-(tributylstannyl)pyridine → 1-(4-Ethylpiperazin-1-yl)-3-(2-methoxypyridin-5-yl)isoquinoline
https://huagongshe.com/reaction/1814531
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxy-5-(tributylstannyl)pyridine | HCID 11729021 | — |
| Reactant | 1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline | HCID 22502447 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1-(4-Ethylpiperazin-1-yl)-3-(2-methoxypyridin-5-yl)isoquinoline | HCID 22503672 | 61.3% |
Reaction Steps
2-Methoxy-5-tributylstannylpyridine (1.41 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.57 g) obtained in Example 28-2 were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.10 g) in xylene in nitrogen atmosphere for 30 min. After cooling, the reaction solution was filtered and extracted in 2N hydrochloric acid. The aqueous layer was washed with ethyl acetate twice. The resulting aqueous layer was 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, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol system), to give 0.38 g of the free compound of the title compound as a pale brown powder.
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-5c93b2b8c6554b95ac28f4cd00757a6d |
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| Source note | uspto-grants-2005_04 |
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