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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019395Generated: November 3, 2026

2-Bromopyridine → HCID 18398987, compound

https://huagongshe.com/reaction/1019395

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18399114HCID 18399114—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
ProductHCID 18398987HCID 18398987—

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of the compound obtained in Example 5 (300 mg), 2-bromopyridine (57 μl), copper iodide (113 mg) and potassium carbonate (82 mg) in dimethylformamide (5 μl) is heated with stirring at 80° C. for five hours. After the reaction is complete, the reaction mixture is extracted with ethyl acetate. The extract is washed with aqueous ammonia, and further washed with water, dried, and concentrated under reduced pressure. The residue is purified by Chromatotron (solvent; hexane:ethyl acetate=1:1) to give 2-[4-(tert-butoxycarbonylamino)phenyl]-6-methoxy-3-methoxycarbonyl-7-(2-pyridyloxy)-4-(3,4,5-trimethoxyphenyl)-1(2H)-isoquinolinone (40 rag) as listed in Table 20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486155B1
Source datasetuspto-grants-2002_11
ORD IDord-bad48635fa3244e8809dddd1177ece23
Source noteuspto-grants-2002_11