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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18697Erstellt: 26. Oktober 2026

Tributylstannane → 1-(4-methoxy-benzenesulfonyl)-2,3-dihydro-1H-indol-7-ylamine

https://huagongshe.com/reaction/18697

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylstannaneHCID 5948—
EduktAzobisisobutyronitrileHCID 6547—
Edukt5-Bromo-1-(4-methoxy-benzenesulfonyl)-2,3-dihydro-1H-indol-7-yl amineHCID 68610232—
LösungsmittelTolueneHCID 1140—
Produkt1-(4-methoxy-benzenesulfonyl)-2,3-dihydro-1H-indol-7-ylamineHCID 2474825490%

Reaktionsschritte

To a stirred solution of 18 (2 g, 4.84 mmol), AIBN (0.08 g, 0.48 mmol), Bu3SnH (3.91 ml, 14.50 mmol) in toluene (49 ml) was heated to reflux for 15 h. After cooling, the reaction mixture was evaporated and then extracted by CH2Cl2. The combined organic layer was dried by MgSO4 and concentrated to give a residue that was purified by silica gel flash column chromatography (EtOAc:n-hexane=1:2) to give compound 19, yield 90%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741495B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3196d557fb8848f3bf1af18536d3e07f
Quellennotizuspto-grants-2010_06