Reacción #725877

ord-2d1bc0ac75dd440e8f3a6fd78cb87d38

Ecuación de reacción

Cc1ccccc1S(=O)(=O)n1cccc1C(=O)c1cc(NC(=O)C(F)(F)F)cc(NC(=O)C(F)(F)F)c1
N-toluenesulfonyl-2-(3,5-di(trifluoroacetylamino)benzoyl)pyrrole
[K+].[OH-]
KOH
Nc1cc(N)cc(C(=O)c2ccc[nH]2)c1
2-(3,5-diaminobenzoyl)pyrrole
Rendimiento 65.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture was heated
  2. 2
    Temperaturaat reflux until TLC analysis
  3. 3
    OtroThe crude product was purified by column chromatography (SiO2, CH2Cl2:MeOH)

Procedimiento

To a stirred EtOH (10 mL) solution of N-toluenesulfonyl-2-(3,5-di(trifluoroacetylamino)benzoyl)pyrrole (1.00 g, 1.83 mmol), was added 40% KOH solution (2 mL) and the mixture was heated at reflux until TLC analysis showed complete conversion. The resulting solution was cooled to room temperature and worked up as in Example 7. The crude product was purified by column chromatography (SiO2, CH2Cl2:MeOH) to afford the purified product 2-(3,5-diaminobenzoyl)pyrrole (237 mg, 65% yield). 1H NMR (500 MHz, CD3OD, 25° C.) δ 2.43 (s, 3H), 6.45 (m, 1H), 6.90 (m, 1H), 7.41 (d, 2H), 7.88 (m, 3H), 7.93 (d, 2H), 8.39 (t, 1H); 13C NMR (100 MHz, CD3OD, 25° C.) δ 104.8, 105.7, 109.4, 119.5, 125.2, 130.5, 139.8, 147.8, 186.0; HRMS (EI): m/z 201.0896 (100) {M}+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691292B2uspto-grants-2010_04