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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992604Generated: October 26, 2026

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

https://huagongshe.com/reaction/1992604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Aminobutan-1-olHCID 12202791—
Reactant7-Bromo-4-chloro-3-nitroquinolineHCID 21984361—
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-bromo-4-chloro-3-nitroquinoline (10.00 g, 34.78 mmol) in dichloromethane (140 mL) was added triethylamine (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 numberUS07648997B2
Source datasetuspto-grants-2010_01
ORD IDord-8ff7da53d6e9481986735a297c4d5aa3
Source noteuspto-grants-2010_01