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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407922Erstellt: 24. Oktober 2026

Sodium Carbonate → (S)-tert-butyl 3-(2,5-difluoro-4-(methylsulfonyl)phenylamino)-2-oxo-1,4'-bipiperidine-1'-carboxylate

https://huagongshe.com/de/reaction/407922

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt1,2,4-Trifluoro-5-(methylsulfonyl)benzeneHCID 46739396—
Edukt(S)-tert-butyl 3-amino-2-oxo-1,4'-bipiperidine-1'-carboxylateHCID 66802275—
LösungsmittelDimethylformamideHCID 6228—
Produkt(S)-tert-butyl 3-(2,5-difluoro-4-(methylsulfonyl)phenylamino)-2-oxo-1,4'-bipiperidine-1'-carboxylateHCID 6747043572,3%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

(S)-tert-butyl 3-amino-2-oxo-1,4′-bipiperidine-1′-carboxylate (4.0 g, 13 mmol), 1,2,4-trifluoro-5-(methylsulfonyl)benzene (Preparation C, 4.2 g, 20 mmol) and Na2CO3 (2.9 g, 27 mmol) were dissolved in DMF (30 mL) and heated at 130° C. overnight. The reaction was concentrated and purified over silica gel (25-75% EtOAc in hexanes) to afford (S)-tert-butyl 3-(2,5-difluoro-4-(methylsulfonyl)phenylamino)-2-oxo-1,4′-bipiperidine-1′-carboxylate (4.6 g, 9.4 mmol, 70% yield) as yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754226B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-95ac0d79b0024d8f8fdbe390394d4565
Quellennotizuspto-grants-2014_06