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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402845Generated: October 25, 2026

Potassium Carbonate → 4-cyclopropyl-1-isopropyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/402845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant4-bromo-1-isopropyl-1H-indole-3-carbaldehydeHCID 77230881—
CatalystHCID 178454869HCID 178454869—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-cyclopropyl-1-isopropyl-1H-indole-3-carbaldehydeHCID 7723087718.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 4-romo-1-(propan-2-yl)-1H-indole-3-carboxaldehyde (120 mg, 0.451 mmol) (from Example 9-1, Step 1) and cyclopropylboronic acid (77 mg, 0.902 mmol) in dioxane (2 mL) and water (0.5 mL) in a 5 mL microwave reaction vial was added potassium carbonate (187 mg, 1.35 mmol) and dichloro[1,1′-bis(di-t-butylphosphino)ferrocene]palladium (II) (29 mg, 0.045 mmol). The reaction was placed under nitrogen, sealed and heated in a microwave reactor at 140° C. for 25 minutes. The solvent was removed in vacuo and the residue was partitioned with ethyl acetate and aqueous sodium bicarbonate and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified on silica gel (COMBI FLASH 24 gm column, gradient of 0-100% ethyl acetate/hexanes) to give the title intermediate (19 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-c464cef29b1846db90279fe2d76f9849
Source noteuspto-grants-2014_06