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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824009Generated: October 30, 2026

Ammonium formate → cis-3-(5-Fluoro-1H-indol-3-yl)-cyclopentylamine

https://huagongshe.com/reaction/1824009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactantcis-benzyl-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamineHCID 68827920—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Productcis-3-(5-Fluoro-1H-indol-3-yl)-cyclopentylamineHCID 68827169—

Reaction Steps

A mixture of cis-benzyl-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine (0.45 g, 1.46 mmol), 0.2 g 10% Pd/C and ammonium formate (1.0 g, 15.9 mmol) in methanol (30 mL) were refluxed under nitrogen for 4 hours. The reaction mixture was cooled, filtered through celite, and concentrated. The residue was diluted with 1 N aqueous NaOH (50 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), then were dried over anhydrous sodium sulfate, filtered and concentrated to give 0.28 g (quant.) of the title compound as a thick oil: MS (ESI) m/z 219 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041697B2
Source datasetuspto-grants-2006_05
ORD IDord-41448dc7b87246edb3ce58c0c86ef518
Source noteuspto-grants-2006_05