تفاعل #11111

معادلة التفاعل

4-Iodo-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione

→

9-Hydroxy-4-iodopyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione

المردود 89.5%

المذيبات

Water

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONwas added in one portion
2. 2
   أخرىto dry
3. 3
   أخرىfreshly-prepared pyridine hydrochloride
4. 4
   أخرىmelt at 200° C. under a CaCl2 drying
5. 5
   استخلاصthe mixture was extracted with EtOAc
6. 6
   تجفيفThe EtOAc extracts were dried
7. 7
   أخرىthe drying agent was removed
8. 8
   تركيزthe solution was concentrated to dryness
9. 9
   أخرىto give a solid which
10. 10
    أخرىwas chromatographed on silica
11. 11
    غسيلElution with EtOAc

الإجراء التجريبي

Powdered 4-Iodo-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione (0.50 g, 1.27 mmol) prepared as in example 6 was added in one portion to dry, freshly-prepared pyridine hydrochloride melt at 200° C. under a CaCl2 drying tube and the mixture was stirred at this temperature for 15 min. Water was added and the mixture was extracted with EtOAc. The EtOAc extracts were dried, the drying agent was removed and the solution was concentrated to dryness to give a solid which was chromatographed on silica. Elution with EtOAc gave 9-Hydroxy-4-iodopyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione (8) (0.43 g, 89%) as an orange powder; mp>350° C. 1H NMR δ [(CD3)2SO] 11.76 (br s, 1H), 11.24 (br s, 1H), 9.29 (br s, 1H), 8.27 (d, J=2.4 Hz, 1H), 8.13 (s, 1H), 7.44 (d, J=8.7 Hz, 1H), 7.08 (dd, J=8.7, 2.4 Hz, 1H). Found: C, 44.90; H, 1.79; N, 7.14. C14H71N2O3 requires C, 44.47; H, 1.87; N, 7.40.

المصدر