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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34359Erstellt: 24. Oktober 2026

1-Piperazinecarboxylic acid, ethyl ester → 9-Bromo-6-(4-ethoxycarbonyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine

https://huagongshe.com/de/reaction/34359

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
EduktSodium HydroxideHCID 14798—
Edukt9-Bromo-1,2dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine-6-oneHCID 13823283—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelTolueneHCID 1140—
Produkt9-Bromo-6-(4-ethoxycarbonyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepineHCID 13823299—

Reaktionsschritte

A stirred mixture of 7.88 g (0.025 mole) of 9-bromo-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine-6-one and 1200 ml toluene was heated under nitrogen until a solution resulted. Then there was added 39.6 g (0.250 mole) of ethyl N-piperazinocarboxylate followed by 14.2g (0.075 mole) of titanium tetrachloride. The mixture was heated under reflux for three hours, cooled to room temperature and treated with 500 ml of 2N sodium hydroxide solution. After stirring vigorously for 15 minutes, the layers were separated. The aqueous phase was extracted with 300 ml of toluene. The toluene layers were combined, washed once with 2N sodium hydroxide solution, twice with water, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was taken up in 25 ml of hot methanol from which 8.5 g (75%) of product crystallized. Recrystallization from ethyl acetate gave the analytical sample, mp 128°-131° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04761412
Quelldatensatzuspto-grants-1988_08
ORD IDord-5abf2a09b39d4f6bb44b8042894ca001
Quellennotizuspto-grants-1988_08