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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818155Generated: October 31, 2026

Water → N-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamide

https://huagongshe.com/reaction/1818155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-(4-aminobutyl)methanesulfonamide hydrochlorideHCID 21984197—
Reactant4-Chloro-3-nitro-7-phenylquinolineHCID 21984335—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamideHCID 2198420382.7%

Reaction Steps

N-(4-aminobutyl)methanesulfonamide hydrochloride (7.8 g, 39 mmol) was added to a suspension of 4-chloro-3-nitro-7-phenylquinoline (35 mmol) and triethylamine (8.0 g, 79 mmol) in NMP (80 mL), and the reaction was stirred at ambient temperature overnight. The resulting solution was poured into water (350 mL) to form a solid, which was isolated by filtration, washed with water, air-dried, and recrystallized from acetonitrile to provide 12.0 g of N-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamide as yellow plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-e1accfaccbfd486495efc1f7efa9b0ae
Source noteuspto-grants-2009_10