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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077209Generated: November 3, 2026

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

https://huagongshe.com/reaction/2077209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant1-Bromo-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 86617062—
SolventDimethylformamideHCID 6228—
Product1-Bromo-4-methoxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl esterHCID 8661708252.3%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 1-bromo-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester (1.89 g, 5.07 mmol), iodomethane (632 μL, 10.13 mmol), cesium carbonate (3.3 g, 10.13 mmol) and dimethylformamide (15 mL) was stirred at 45° C. for sixteen hours before it was quenched with water, extracted with ethyl acetate. The organic layer was washed with water, brine, dried over 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 (1.03 g): MS: (+) m/z 387.64, 389.75 (M+1, 79Br/81Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928120B2
Source datasetuspto-grants-2011_04
ORD IDord-fbadac269da54c938b862798cc5ccdb5
Source noteuspto-grants-2011_04