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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273314Erstellt: 26. Oktober 2026

Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-4-azaindole

https://huagongshe.com/reaction/273314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
Edukt4-AzaindoleHCID 9226—
EduktSodium hydrideHCID 24758—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelHexaneHCID 8058—
Produkt1-(Phenylsulfonyl)-4-azaindoleHCID 4527076683%

Reaktionsschritte

Sodium hydride (60% in mineral oil, 203 mg, 5.08 mmol) was washed twice with hexane, and the residue suspended in DMSO (5 ml). 1H-Pyrrolo[3,2-b]pyridine (500 mg, 4.24 mmol) was added and the reaction stirred for 15 minutes. Benzenesulphonyl chloride (749 mg, 4.42 mmol) was added rapidly and the reaction stirred for 0.5 h. After quenching with water the product was extracted into EtOAc, dried (Na2SO4) and concentrated in vacuo. Chromatography (EtOAc, silica) yielded the title compound as a white crystalline solid (903 mg, 83%). δH (d6-DMSO) 8.48 (1H, dd, J 0.8, 3.8 Hz), 8.31 (1H, m), 8.15 (1H, d, J 3.8 Hz), 8.04 (2H, m), 7.72 (1H, m,), 7.61 (2H, m,), 7.36 (1H, dd, J 4.7, 8.4 Hz), 6.98 (1H, dd, J 0.8, 3.8 Hz). LCMS (ES+) RT 3.056 minutes, 259 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456286B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-7afaea33b9224b6aba0d9aaf3a6888a7
Quellennotizuspto-grants-2008_11