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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 873666Erstellt: 24. Oktober 2026

9-Acetyl-9H-carbazole → HCID 66850646, Verbindung

https://huagongshe.com/de/reaction/873666

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt9-Acetyl-9H-carbazoleHCID 95837—
Edukt3-(Aminosulfonyl)-4-chlorobenzoyl chlorideHCID 3017979—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 66850646HCID 66850646—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 1 g of 1-carbazol-9-yl-ethanone and 2.43 g of 4-chloro-3-sulfamoyl-benzoyl chloride in methylene chloride (20 mL) is added 2.55 g of aluminum chloride. The mixture is stirred at 50° C. overnight. The solution is then cooled at −78° C., quenched with a 6 N HCl solution and allowed to warm up to room temperature. Methylene chloride is added to dissolve the precipitate and the solution is extracted, washed with a saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. The residue is loaded on Celite and purified by silica gel chromatography (1:1 hexanes/ethyl acetate) to afford 5-(9-acetyl-9H-carbazole-2-carbonyl)-2-chloro-benzenesulfonamide as yellow foam. MS (m/z): 427 (M+1). HPLC Reverse Phase (Nucleosil 100-5 C18, gradient 10→100% CH3CN in 5 min) room temperature=5.35 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08975439B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-b058d22797e14c7aaa7d8336d8ca5540
Quellennotizuspto-grants-2015_03