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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077210Generated: November 3, 2026

1-Bromo-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester → 1-Cyano-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/2077210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 86617082—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
Product1-Cyano-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 6711048882.7%

Reaction Steps

A mixture of 1-bromo-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester (1.02 g, 2.63 mmol), copper (I) cyanide (470 mg, 5.25 mmol) and anhydrous dimethylformamide (8.8 mL) was refluxed for ten minutes before it was cooled to room temperature quenched with water and ethyl acetate. The slurry was filtered. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate, concentrated in vacuo and the residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a yellow solid (727 mg): MS: (+) m/z 334.83 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928120B2
Source datasetuspto-grants-2011_04
ORD IDord-686686b115bf4f28a322df65b68b73e3
Source noteuspto-grants-2011_04