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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61687Generated: October 28, 2026

HCID 66834104, compound → 2-[1-(6-Cyano-1-methanesulfonyl-1H-indol-2-yl)-1-methylethyl]-4-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/61687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66834104HCID 66834104—
Reactant2-(1,1-Dimethylprop-2-ynyl)-4-methoxy-benzoic acid methyl esterHCID 86663815—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
Product2-[1-(6-Cyano-1-methanesulfonyl-1H-indol-2-yl)-1-methylethyl]-4-methoxy-benzoic acid methyl esterHCID 6683428262%

Reaction Conditions

Temperature90 °C

Reaction Steps

To the DMF (2 ml) solution of 2-(1,1-dimethylprop-2-ynyl)-4-methoxy-benzoic acid methyl ester (Compound AA3, 134 mg, 0.577 mmol) and N-(2-bromo-5-cyanophenyl)methanesulfonamide (Compound AA3, 167 mg, 1.05 eq.), copper iodide (9 mg, 0.08 eq.) and TEA (129 μl, 1.6 eq.) were added, degassed and flushed with nitrogen gas, added with dicholorobis(triphenylphosphine) palladium (20 mg, 0.05 eq.), and then degassed and flushed again with nitrogen gas. After stirring for 2 hr at 90° C., the reaction solution was added with water, extracted with ethyl acetate. The organic layer was washed with an brine and dried over magnesium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (white solid, 152 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440922B2
Source datasetuspto-grants-2016_09
ORD IDord-a58d2fd7fa4f4359a8324c9c29e54fd3
Source noteuspto-grants-2016_09