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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1684563Erstellt: 26. Oktober 2026

Dansyl chloride → 5-(dimethylamino)-N-(5-bromo-3-methyl-2-pyridyl)-1-naphthalenesulphonamide

https://huagongshe.com/reaction/1684563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDansyl chlorideHCID 11801—
Edukt2-Amino-5-bromo-3-methylpyridineHCID 137934—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
Produkt5-(dimethylamino)-N-(5-bromo-3-methyl-2-pyridyl)-1-naphthalenesulphonamideHCID 10645779—

Reaktionsschritte

A solution of 5-dimethylamino-1-naphthalenesulphonyl chloride (269.5 mg), 2-amino-5-bromo-3-methylpyridine (187 mg) and 4-dimethylaminopyridine (100 mg) in pyridine (5 ml) was heated at 85° C. for 18 hours. Volatile material was removed by evaporation and dichloromethane (50 ml) was added. Insoluble material was removed by filtration and the filtrate was concentrated by evaporation. The residue was purified by flash chromatography, eluting with ethyl acetate/hexane (1:1 v/v), to give 5-(dimethylamino)-N-(5-bromo-3-methyl-2-pyridyl)-1-naphthalenesulphonamide as a foam (135) mg); NMR (CDCl3): 2.2(s, 3H), 2.9(s, 6H), 7.15 (d, 1H), (7.4-7.8(m, 4H), 8.4(d, 1H), 8.5(d, 2H); mass spectrum (+ve CI): 420 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05641793
Quelldatensatzuspto-grants-1997_06
ORD IDord-f0d04c2a21534de4970c9509173e77ce
Quellennotizuspto-grants-1997_06