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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572126Generated: November 3, 2026

2,8-Dichloro-quinoline-3-carbaldehyde → 8-Chloro-2-(6-methoxypyrazin-2-yl)quinoline-3-carbaldehyde

https://huagongshe.com/reaction/572126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,8-Dichloro-quinoline-3-carbaldehydeHCID 14917125—
Reactant2-Methoxy-6-(tributylstannyl)pyrazineHCID 16427103—
Solvent1,4-DioxaneHCID 31275—
Product8-Chloro-2-(6-methoxypyrazin-2-yl)quinoline-3-carbaldehydeHCID 8670116863.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2,8-dichloroquinoline-3-carbaldehyde (0.5 g, 2.21 mmol), 2-methoxy-6-(tributylstannanyl)pyrazine (1.0 g, 2.51 mmol) and tetrakis(triphenyl-phosphine)palladium(0) (0.2 g, 0.173 mmol) in 1,4-dioxane (10 mL) was degassed and heated at 110° C. overnight. The mixture was allowed to cool to room temperature and diluted with EtOAc. The resulting solid was collected by filtration, washed with EtOAc, then ether, and dried to give the title compound (0.42 g, 63%) as a yellow solid. δH(DMSO-d6) 10.58 (s, 1H), 9.24 (s, 1H), 8.93 (s, 1H), 8.53 (s, 1H), 8.27 (dd, J 8.3, 1.2 Hz, 1H), 8.17 (dd, J 7.5, 1.2 Hz, 1H), 7.75 (m, 1H), 3.96 (s, 3H). LCMS (ES+) 300 (M+H)+, RT 1.51 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029392B2
Source datasetuspto-grants-2015_05
ORD IDord-3e2e90a550e94e229125eb32bf4e785c
Source noteuspto-grants-2015_05