HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → N-[(1S)-1-(3-aminophenyl)ethyl]-6-bromopyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Indium | HCID 5359967 | — |
| Reactant | 6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amine | HCID 86641856 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[(1S)-1-(3-aminophenyl)ethyl]-6-bromopyridin-2-amine | HCID 86641857 | 77.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029386B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-2943542f228746ac918d7e9fcb6cb2db |
| Source note | uspto-grants-2015_05 |