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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072452Generated: October 30, 2026

Ammonium formate → trans-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine

https://huagongshe.com/reaction/1072452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactanttrans-benzyl-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamineHCID 68830416—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttrans-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamineHCID 68827696100%

Reaction Steps

A mixture of trans-benzyl-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine (0.45 g, 1.46 mmol), 0.20 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 (100%) of the title compound as a thick oil: MS (ESI) m/z 219 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911445B2
Source datasetuspto-grants-2005_06
ORD IDord-acfa7053bfbf469abdfc8e3ad3dabba3
Source noteuspto-grants-2005_06