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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706130Generated: October 31, 2026

Dimethylformamide → 1-Cyano-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/706130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChloroform isopropyl alcoholHCID 21906603—
Reactant1-Bromo-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 86617062—
ReactantHCID 178418546HCID 178418546—
SolventWaterHCID 962—
Product1-Cyano-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 6711010754.3%

Reaction Steps

A mixture of 1-bromo-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester (1.22 g, 3.3 mmol), copper(I) cyanide (585 mg, 6.6 mmol), and anhydrous dimethylformamide (16 mL) was refluxed for ten minutes before it was cooled to room temperature and diluted with water. To the resulting slurry was added a chloroform/isopropanol mixture (3:1, 150 mL). After stirring for 10 minutes the solid components were separated by filtration and discarded. The organic layer of the filtrate was washed with water, and brine before it was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of methanol and dichloromethane to give the title compound as a white solid (574 mg): 1H NMR (CDCl3, 200 MHz): δ=12.26 (s, 1H), 8.15 (m, 1H), 7.71 (t, J=8.2 Hz, 1H), 7.38 (m, 2H), 7.17 (m, 4H), 4.12 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174976B2
Source datasetuspto-grants-2015_11
ORD IDord-9a26b6eaf1a84eef8eaface5a9ad5646
Source noteuspto-grants-2015_11