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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079898Generated: October 26, 2026

Potassium Hydroxide → 4-(1-cyclopentyl-6-nitro-1H-indol-3-yl)-benzonitrile

https://huagongshe.com/reaction/2079898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantCyclopentyl 4-methylbenzene-1-sulfonateHCID 317685—
Reactant4-(6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442197—
SolventDimethyl SulfoxideHCID 679—
Product4-(1-cyclopentyl-6-nitro-1H-indol-3-yl)-benzonitrileHCID 5744224458%

Reaction Steps

Method M Add KOH pellets (200 mg, 3.42 mmol) to a solution of 4-(6-nitro-1H-indol-3-yl)-benzonitrile, 9, (150 mg, 0.57 mmol) in DMSO (10 mL). After the KOH pellets dissolve, add cyclopenyl tosylate (210 mg, 0.85 mmol) in DMSO (3 mL). Allow the reaction mixture to stir overnight at ambient temperature. Add additional cyclopentyl tosylate (210 mg, 0.85) and allow the reaction mixture to stir for another 6 h. Add still more cyclopentyl tosylate (210 mg, 0.85 mmol) and allow the reaction mixture to stir overnight at ambient temperature. Quench the resulting reaction mixture with 5N HCl/ice. Extract the quenched reaction mixture with EtOAc. Wash the EtOAc extracts with brine. Dry the organic layer over MgSO4, filter, and remove the solvent from the filtrate to provide a solid. Purify by silica gel column chromatography (0-100% EtOAc/hexanes gradient) and collect the fractions and remove the solvent to afford 110 mg (58%) of the title compound. LRMS (API ES+)=332.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932284B2
Source datasetuspto-grants-2011_04
ORD IDord-59925e9d0a3643939c0cd70ec81fdb67
Source noteuspto-grants-2011_04