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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187414Generated: October 26, 2026

3-Aminobutan-1-ol → 3-[(7-Bromo-3-nitroquinolin-4-yl)amino]propan-1-ol

https://huagongshe.com/reaction/1187414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobutan-1-olHCID 12202791—
Reactant7-Bromochloro-3-nitroquinolineHCID 86611497—
SolventDichloromethaneHCID 6344—
Product3-[(7-Bromo-3-nitroquinolin-4-yl)amino]propan-1-olHCID 66619878100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-bromochloro-3-nitroquinoline (10.00 g, 34.78 mmol) in dichloromethane (140 mL) was added triethylanine (10.2 mL, 73.1 mmol). The solution was cooled to 0° C., and 3-amino-1-butanol (2.80 mL, 36.5 mmol) was added. The solution was stirred overnight at ambient temperature and then filtered to collect a precipitate. The precipitate was washed with dichloromethane and water. The filtrate was washed with saturated aqueous sodium bicarbonate and then added to the precipitate. The mixture was concentrated under reduced pressure. Methanol and toluene were added several times and removed under reduced pressure. The resulting solid was dried under high vacuum to provide 11.34 g of 3-[(7-bromo-3-nitroquinolin-4-yl)amino]propan-1-ol as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673932B2
Source datasetuspto-grants-2014_03
ORD IDord-9b68e56957564099971895a949267d6f
Source noteuspto-grants-2014_03