反应详情

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.

1. customequipped with a magnetic stirrer and a nitrogen inlet
2. temperaturewas heated
3. temperatureto reflux at an oil bath temperature of ~250° C. under a nitrogen atmosphere
4. customwas consumed
5. additionwas poured into a 1 liter beaker
6. additioncontaining 400 milliliters of ice cold 5 percent of HCl
7. customThe yellow precipitate obtained
8. customwas isolated by filtration
9. washAfter washing with water (~200 milliliters) and ~20 milliliters of methanol and vacuum
10. customdrying
11. custom4.7 grams of crude product resulted
12. customThis product was then recrystallized from a mixture of (dimethylformamide) DMF/MeOH/H2O (~30 milliliter each)