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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18432Erstellt: 23. Oktober 2026

3-Chloropropanesulphonyl chloride → N-{5-[3-(1,1-dioxido-2-isothiazolidinyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamide

https://huagongshe.com/de/reaction/18432

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloropropanesulphonyl chlorideHCID 15410—
EduktSodium hydrideHCID 24758—
EduktDiisopropylethylamineHCID 81531—
EduktN-[5-(3-aminophenyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamideHCID 46899970—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-{5-[3-(1,1-dioxido-2-isothiazolidinyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamideHCID 115756869,2%

Reaktionsschritte

A mixture of N-[5-(3-aminophenyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide (100 mg, 0.30 mmol), and diisopropylethylamine (79 mg, 0.61 mmol), in dry dimethylformamide (2 ml) was treated with 3-chloropropanesulfonyl chloride (54 mg, 0.30 mmol) and stirred at room temperature for 1 h. Sodium hydride (60% dispersion in oil, 15 mg, 0.38 mmol) was added and the mixture stirred at 60° C. for 0.5 h. The reaction mix was cooled then partitioned between dichloromethane and 0.5M hydrochloric acid, and the organic layer was evaporated under reduced pressure to give a brown oil which was purified by column chromatography on a 5 g isolute silica sep-pak column eluting from 0-50% ethyl acetate in 40-60° C. petroleum ether to give the title compound as a yellow oil (12 mg, 9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741351B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-cf415d9399974ffea9b7863d9a6fca64
Quellennotizuspto-grants-2010_06