Reacción #11110

Ecuación de reacción

Diphenylphosphoryl azide

9-methoxy-1,3-dioxo-1,2,3,6-tetrahydropyrrolo[3,4-c]carbazole-4-carboxylic acid

Et3N

→

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

Rendimiento 93.4%

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

Rendimiento 93.4%

Disolventes

t-butanol

CH2Cl2 trifluoroacetic acid

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturathe mixture was refluxed under an atmosphere of nitrogen for 16 h
2. 2
   ConcentraciónThe solution was concentrated in vacuo
3. 3
   Otrothe residue partitioned between EtOAc and saturated aqueous NaHCO3
4. 4
   OtroInsoluble material was removed by filtration of the two layers through Celite
5. 5
   Lavadowashing through with more EtOAc
6. 6
   OtroThe organic phase was dried
7. 7
   Otrothe drying agent was removed
8. 8
   Concentraciónthe solution was concentrated to dryness
9. 9
   Otrogave a yellow solid
10. 10
    ConcentraciónAfter concentration in vacuo the residue
11. 11
    Otrowas partitioned between EtOAc and saturated aqueous NaHCO3 solution
12. 12
    SecadoThe EtOAc solution was dried
13. 13
    Otrothe drying agent was removed
14. 14
    Concentraciónthe solution was concentrated to dryness
15. 15
    Otroto give an orange solid which
16. 16
    Otrochromatographed
17. 17
    LavadoElution with ethyl acetate/petroleum ether (1:1)

Procedimiento

Diphenylphosphoryl azide (1.81 mL, 8.38 mmol) was added to a mixture of the 9-methoxy-1,3-dioxo-1,2,3,6-tetrahydropyrrolo[3,4-c]carbazole-4-carboxylic acid (2.55 g, 8.22 mmol), prepared as in example 4, and Et3N (1.17 mL, 8.38 mmol) in anhydrous t-butanol (300 mL) and the mixture was refluxed under an atmosphere of nitrogen for 16 h. The solution was concentrated in vacuo and the residue partitioned between EtOAc and saturated aqueous NaHCO3. Insoluble material was removed by filtration of the two layers through Celite, washing through with more EtOAc. The organic phase was dried, the drying agent was removed and the solution was concentrated to dryness and gave a yellow solid. This material was dissolved in CH2Cl2/trifluoroacetic acid (1:1) (200 mL) and the solution was held at room temperature for 1 h. After concentration in vacuo the residue was partitioned between EtOAc and saturated aqueous NaHCO3 solution. The EtOAc solution was dried, the drying agent was removed and the solution was concentrated to dryness to give an orange solid which was adsorbed onto silica and chromatographed. Elution with ethyl acetate/petroleum ether (1:1) followed by ethyl acetate and then methanol/ethyl acetate (1:9) gave 4-amino-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione (6) as an orange powder (2.16 g, 93%), mp 342–345° C. 1H NMR δ [(CD3)2SO] 11.18 (s, 1H), 10.78 (br s, 1H), 8.18 (d, J=2.5 Hz, 1H), 7.29 (d, J=8.7 Hz, 1H), 7.01 (dd, J=8.7, 2.5 Hz, 1H), 6.83 (s, 1H), 6.28 (br s, 2H), 3.82 (s, 3H). Found: C, 63.05; H, 3.99; N, 14.05. C15H11N3O3, 1/2H2O requires C, 63.04; H, 4.06; N, 14.7.

Fuente