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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535870Erstellt: 25. Oktober 2026

Sodium hydride → HCID 58459895, Verbindung

https://huagongshe.com/reaction/535870

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2-Chloro-1-piperidine-1-yl-ethanoneHCID 222312—
Edukt2,3,4,9,10,10a-hexahydro-1H-3a,8,9-triaza-cyclopenta[b]fluoreneHCID 67036560—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 58459895HCID 58459895—

Reaktionsschritte

To a solution of 7,8,9,9a,10,11-hexahydro-5H-pyrido[3′,2′:4,5]pyrrolo[3,2-f]indolizine (70 mg, 0.32 mmol) in DMF (1 mL) was added a suspension of NaH (40.0 mg, 0.986 mmol) in DMF (1 mL). After stirring for 5 min at RT, a solution of 2-chloro-1-(piperidin-1-yl)ethanone (159 mg, 0.986 mmol) in DMF (1 mL) was added dropwise into the reaction mixture and stiffing continued for another 3 h. The progress of reaction was monitored by TLC and NMR. The reaction mixture was diluted with ice-water (20 mL) and extracted with EtOAc (3×25 mL). The organic layer was washed with water (3×20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford crude material, which was purified by silica gel flash chromatography (10% MeOH-DCM) to yield 1-(piperidin-1-yl)-2-(8,9,9a,10-tetrahydro-5H-pyrido[3′,2′:4,5]pyrrolo[3,2-f]indolizin-11(7H)-yl)ethanone;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859561B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-82c93003d63f494ebfd5d4ece434e888
Quellennotizuspto-grants-2014_10