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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818176Generated: November 1, 2026

Water → (7-Bromo-3-nitroquinolin-4-yl)-(5-chloropentyl)amine

https://huagongshe.com/reaction/1818176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21984273HCID 21984273—
SolventDichloromethaneHCID 6344—
Product(7-Bromo-3-nitroquinolin-4-yl)-(5-chloropentyl)amineHCID 21984402—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 5-(7-bromo-3-nitroquinolin-4-ylamino)pentan-1-ol (0.92 g, 2.6 mmol) in dichloromethane (13 mL) was cooled to 0° C.; thionyl chloride was added dropwise. The reaction was stirred for five minutes at 0° C. then allowed to warm to ambient temperature and stirred overnight. Saturated aqueous sodium bicarbonate (25 mL) was slowly added followed by water (25 mL). The aqueous layer was separated and extracted with dichloromethane (3×50 mL), and the combined organic fractions were dried over magnesium sulfate and concentrated under reduced pressure to provide 0.91 g of (7-bromo-3-nitroquinolin-4-yl)-(5-chloropentyl)amine as a yellow semisolid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-bc04bbb9b0ab4733a3a97b0655fe2813
Source noteuspto-grants-2009_10