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HRID 553048Erstellt: 26. Oktober 2026

Cesium carbonate → 5-(9H-Fluoren-2-yl)-hexahydropyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/553048

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt2-Bromo-9H-fluoreneHCID 14336—
EduktTert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt5-(9H-Fluoren-2-yl)-hexahydropyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl esterHCID 6716374558,1%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of 3-Boc-3,7-diazabicyclo[3.3.0]octane (340 mg, 1.6 mmol; see WO 0181347), 2-bromofluorene (0.47 g, 1.9 mmol), tris(dibenzylideneacetone)dipalladium (0) (Pd2(dba)3; 44 mg, 0.048 mmol; Strem), racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP; 50 mg, 0.080 mmol; Strem) and Cs2CO3 (1.0 g, 3.2 mmol; Aldrich) in toluene (25 mL) in a sealed tube was warmed to 85° C. and stirred for 18 h. The material was cooled to ambient temperature, filtered, concentrated under reduced pressure and purified by flash chromatography (silica gel, 50% gradient of EtOAc in hexanes) to afford the title compound (350 mg, 0.93 mmol; 58% yield): MS (DCI/NH3) m/z 377 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951791B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-7d83b38a47b246ec96fb11935f3c58f2
Quellennotizuspto-grants-2011_05