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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20990Generated: October 25, 2026

Water → tert-Butyl 5-(4-methylpiperazin-1-yl)-1H-indole-1-carboxylate

https://huagongshe.com/reaction/20990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant1-MethylpiperazineHCID 53167—
Reactant5-Iodo-1H-indole, N-BOC protectedHCID 16125958—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Producttert-Butyl 5-(4-methylpiperazin-1-yl)-1H-indole-1-carboxylateHCID 5811740528%

Reaction Steps

1-(tert-Butoxycarbonyl)-5-iodoindole (3.46 g, 10.1 mmol) was dissolved in toluene (45.0 mL), and the solution was added with 4-methylpiperazine (2.24 mL, 20.2 mmol), 2,2′-(diphenylphosphino)-1,1′-binaphthyl (1.26 g, 2.02 mmol), cesium carbonate (4.94 mg, 15.2 mmol) and palladium acetate (226 mg, 1.01 mmol), followed by stirring under reflux for 24 hours. The mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography (chloroform/methanol=9/1) to obtain 1-(tert-butoxycarbonyl)-5-(4-methylpiperazino)indole (887 mg, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-9b5aef98020e4bc380e5b6f42844c23d
Source noteuspto-grants-2010_06