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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654348Erstellt: 24. Oktober 2026

Aniline → 2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamide

https://huagongshe.com/de/reaction/654348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
EduktPhenyl2-hydroxy-11H-benzo[a]carbazole-3-carboxylateHCID 19933809—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamideHCID 15596992166,2%

Reaktionsschritte

The phenyl 2-hydroxy-11H-benzo(a)carbazole-3-carboxylate obtained from Example I (5 grams, 14 millimoles), aniline (2.75 grams, 28 millimoles) and 15 milliliters of N-methyl pyrrolidinone were charged in a 100 milliliter 3-neck flask equipped with a magnetic stirrer and a nitrogen inlet. The resulting mixture was stirred and was heated to reflux at an oil bath temperature of ~250° C. under a nitrogen atmosphere. After 3 hours, TLC analysis revealed that all the starting phenyl ester was consumed. The mixture was cooled to room temperature and was poured into a 1 liter beaker containing 400 milliliters of ice cold 5 percent of HCl. The yellow precipitate obtained was isolated by filtration. After washing with water (~200 milliliters) and ~20 milliliters of methanol and vacuum drying, 4.7 grams of crude product resulted. This product was then recrystallized from a mixture of (dimethylformamide) DMF/MeOH/H2O (~30 milliliter each) yielding 4.1 grams (83 percent) of 2-hydroxy-11H-benzo(a)carbazole-3-carboxanilide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05130443
Quelldatensatzuspto-grants-1992_07
ORD IDord-e182c9a22cc24161b9e73f13b2aeca9b
Quellennotizuspto-grants-1992_07