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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378895Erstellt: 25. Oktober 2026

Potassium Carbonate → (4-Bromo-2-methyl-phenyl)-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanone

https://huagongshe.com/reaction/378895

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
Edukt4-Bromo-2-methylbenzoyl chlorideHCID 12846483—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDiethylformamideHCID 12051—
Produkt(4-Bromo-2-methyl-phenyl)-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanoneHCID 1554704953,4%

Reaktionsschritte

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine (3 g, 15.2 mmol) in N,N-dimethylformamide under nitrogen was added solid potassium carbonate (6.3 g, 45.6 mmol). A solution of the crude 4-bromo-2-methylbenzoyl chloride (22.8 mmol) in N,N-diethylformamide was added dropwise, and the mixture stirred at room temperature for 15 minutes. Excess potassium carbonate was filtered off, the filtrate was washed with water and the aqueous layer was extracted with chloroform. The extracts were dried over anhydrous sodium sulfate, evaporated to dryness and the residue dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided the title compound (3.2 g) as a foam which crystallized upon sonication from ethanol hexane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06297234B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-15891177812a46ce937adeb4342eb50b
Quellennotizuspto-grants-2001_10