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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251213Generated: October 30, 2026

2-Methoxy-5-(tributylstannyl)pyridine → 1-(4-Ethylpiperazin-1-yl)-3-(2-methoxypyridin-5-yl)isoquinoline

https://huagongshe.com/reaction/1251213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-5-(tributylstannyl)pyridineHCID 11729021—
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
Product1-(4-Ethylpiperazin-1-yl)-3-(2-methoxypyridin-5-yl)isoquinolineHCID 2250367261.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-ae92ff8bc1724b39920e3911c2fade68
Source noteuspto-grants-2002_01