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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260883Erstellt: 24. Oktober 2026

Water → N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide

https://huagongshe.com/de/reaction/260883

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-Aminoindan hydrochlorideHCID 122764—
Edukt4-(N-methylacetamido)benzene-1-sulfonyl chlorideHCID 293146—
EduktSodium AcetateHCID 517045—
LösungsmittelEthanolHCID 702—
ProduktN-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamideHCID 2291894795%

Reaktionsschritte

2-Indanylamine hydrochloride (9.68 g, 57.1 mmol) was added to a suspension of the 4-(N-acetyl-N-methylamino)benzenesulfonyl chloride (12.84 g, 51.9 mmol) prepared in Preparative Example 12 and sodium acetate (18.73 g) in ethanol (100 ml). The obtained mixture was stirred at room temperature for 3 hours, followed by the addition of water. The obtained mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of common salt, dried over magnesium sulfate, and concentrated to give N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide as a white crystal (16.92 g, 95%). Ethanol (80 ml) and 1N aqueous sodium hydroxide (80 ml) were added to the white crystal. The obtained mixture was heated under reflux overnight, acidified with 1N aqueous hydrochloric acid, adjusted to pH 8 with sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to precipitate a crystal. This crystal was recovered by filtration and washed with ether to give the title compound as a white crystal (6.79 g, 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05530118
Quelldatensatzuspto-grants-1996_06
ORD IDord-2cade1d80de54dd4a5d051bbc3917325
Quellennotizuspto-grants-1996_06