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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572207Generated: October 25, 2026

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

https://huagongshe.com/reaction/572207

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 numberUS09029386B2
Source datasetuspto-grants-2015_05
ORD IDord-2943542f228746ac918d7e9fcb6cb2db
Source noteuspto-grants-2015_05