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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160827Generated: November 3, 2026

Toluene → methyl 2-{3-cyano-4-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]phenyl}isonicotinate

https://huagongshe.com/reaction/1160827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Triisopropylsilyl)pyrrole-3-boronic acidHCID 2763303—
ReactantMethyl 2-(3-cyano-4-([(trifluoromethyl)sulfonyl]oxy)phenyl)isonicotinateHCID 86616562—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Productmethyl 2-{3-cyano-4-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]phenyl}isonicotinateHCID 669954305.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

58 mg of tetrakis(triphenylphosphine)palladium and 208 mg of potassium carbonate were added to a toluene (10 ml) solution of 386 mg of methyl 2-(3-cyano-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)isonicotinate and 534 mg of 1-(triisopropylsilyl)pyrrole-3-boronic acid, then this was irradiated with microwaves and heated at 130° C. in a nitrogen atmosphere for 1 hour. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5 to 70:30) to obtain 24 mg of methyl 2-{3-cyano-4-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]phenyl}isonicotinate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816558B2
Source datasetuspto-grants-2010_10
ORD IDord-971291149a64418383462c801f215b18
Source noteuspto-grants-2010_10