Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 528825Erstellt: 26. Oktober 2026

Benzoyl chloride, 3,4-dichloro- → 1-(3,4-Dichlorobenzoyl)indoline-5-sulfonamide

https://huagongshe.com/reaction/528825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chloride, 3,4-dichloro-HCID 76403—
Edukt2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
Edukt1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
Produkt1-(3,4-Dichlorobenzoyl)indoline-5-sulfonamideHCID 7106076436,3%

Reaktionsschritte

Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 195 mg, 0.98 mmol) and 3,4-dichlorobenzoyl chloride (412 mg, 1.97 mmol) were converted to the title compound (132 mg, 36%) after purification using preparative HPLC. 1H NMR (DMSO-d6) δ 7.92 (d, J=1.1 Hz, 1H), 7.78 (d, J=8.1 Hz, 1H), 7.71-7.61 (m, 3H), 7.26 (s, 2H), 4.07 (t, J=8.3 Hz, 2H), 3.16 (t, J=8.2 Hz, 2H); MS(ESI+) m/z 370.8 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346795B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-eba422339fb24e8b99caeb21989720c3
Quellennotizuspto-grants-2016_05