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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255829Generated: October 25, 2026

Ammonium Chloride → N-[(1S)-1-(3-aminophenyl)ethyl]-6-bromopyridin-2-amine

https://huagongshe.com/reaction/1255829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantIndiumHCID 5359967—
Reactant6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amineHCID 86641856—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-[(1S)-1-(3-aminophenyl)ethyl]-6-bromopyridin-2-amineHCID 8664185777.3%

Reaction Steps

To a solution of 6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amine (100 mg, 0.31 mmol) in ethanol (5 mL) was added a solution of ammonium chloride (166 mg, 3.1 mmol) in water (2.5 mL), then indium powder (142 mg, mesh 100, 1.24 mmol). The mixture was heated at reflux for 4.5 hours, was allowed to cool to room temperature and was filtered through Celite. The filter cake was washed with water and ethanol and the combined filtrates were extracted with dichloromethane (2×30 mL) and the extracts washed with brine (30 mL), dried (Na2SO4) and concentrated under reduced pressure to give N-[(1S)-1-(3-aminophenyl)ethyl]-6-bromopyridin-2-amine (70 mg, 77%) as a dark yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461161B2
Source datasetuspto-grants-2013_06
ORD IDord-6fd67f33b2c94ed4a2a2ac85edb7d796
Source noteuspto-grants-2013_06