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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175346Generated: October 29, 2026

Ammonium Acetate → 1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanamine

https://huagongshe.com/reaction/2175346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanoneHCID 58565366—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanamineHCID 5856535196.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 1-[1-(3-fluorophenyl)-3-methyl-1H-indol-2-yl]ethanone (0.165 g, 0.617 mmol) and ammonium acetate (0.476 g, 6.17 mmol) in methanol (2.0 mL) and acetonitrile (2.0 mL) was heated at 65° C. in a sealed tube for 1 hour. After cooling to room temperature, sodium cyanoborohydride (0.12 g, 1.9 mmol) was added to the resultant mixture. The reaction was heated at 65° C. over the weekend. The reaction was cooled to room temperature and quenched with saturated NaHCO3 solution and then extracted with dichloromethane, dried over MgSO4 and concentrated to give the crude amine (0.16 g), which was used directly in next step. LCMS calculated for C17H18FN2(M+H)+: m/z=269.1. Found: 252.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062055B2
Source datasetuspto-grants-2015_06
ORD IDord-d0f917a4a43740829fa8f313a35afcb8
Source noteuspto-grants-2015_06