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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 876214Erstellt: 25. Oktober 2026

Acetonitrile → 3-Tetrahydrofuran-3-yl-3,8-diazabicyclo[3.2.1]octane

https://huagongshe.com/reaction/876214

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktN-bromobutanimideHCID 67184—
Edukttert-Butyl 4-(2-oxo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylateHCID 67472855—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Tetrahydrofuran-3-yl-3,8-diazabicyclo[3.2.1]octaneHCID 9041401499%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

Tert-butyl 4-(2-oxoindolin-1-yl)piperidine-1-carboxylate (100 mg, 0.32 mmol) in ACN is cooled down to −10° C., N-bromosuccinimide (56.47 mg, 0.32 mmol) is added and stirred at −10° C. for 2 h. The reaction mixture is diluted with dichlormethane and water. The organic layer is separated, dried and concentrated. The crude product is used for the next step without further purification. Yield 99%, m/z 395 [M+H]+, rt 1.126 min, LC-MS Method Z020_S01.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987249B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-da02d577f2cd441789b6783cfa870619
Quellennotizuspto-grants-2015_03