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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 528828Erstellt: 25. Oktober 2026

Benzoyl chloride → 1-Benzoylindoline-5-sulfonamide

https://huagongshe.com/reaction/528828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
Edukt2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
Edukt1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
Produkt1-Benzoylindoline-5-sulfonamideHCID 1768113779%

Reaktionsschritte

Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 100 mg, 0.50 mmol) and benzoyl chloride (64 μL, 0.56 mmol) were converted to the title compound (120 mg, 79%). 1H NMR (DMSO-d6) δ 7.70 (s, 1H), 7.65-7.60 (m, 3H), 7.57-7.49 (m, 4H), 7.24 (s, 2H), 4.07 (t, J=8.5 Hz, 2H), 3.15 (t, J=8.4 Hz, 2H); MS(ESI+) m/z 303.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346795B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-e980f2a76d114151a079ad587acb17b1
Quellennotizuspto-grants-2016_05