Reacción #51428

Ecuación de reacción

Compound 78

Ethyl-(2-{[1-(5-nitro-1H-indol-2-yl)-methanoyl]-amino}-ethyl)-carbamic acid dimethyl-ethyl ester

1H-indole-2,5-dicarboxylic acid bis-(pentafluorophenyl-amide)

1H-Indole-2,5-dicarboxylic acid bis-(pentafluorophenyl-amide)

→

76

Rendimiento 40.0%

1H-Indole-2,5-dicarboxylic acid bis-{[2-(2-ethylamino-ethylcarbamoyl)-1H-indol-5-yl]-amide}

Rendimiento 40.0%

Disolventes

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe solvent was evaporated to dryness
2. 2
   workup.DISSOLUTIONThe residue was dissolved in 5 ml of TFA/anisole (8:2)
3. 3
   workup.WAITthe mixture was kept at room temperature for 1 h
4. 4
   OtroThe product was precipitated by ether
5. 5
   Otropurified by HPLC

Procedimiento

Compound 78 (127 mg, 0.336 mmol) was reduced to 79 by hydrogenation according to general procedure A in example 10. A mixture of above amine DS13a and 1H-indole-2,5-dicarboxylic acid bis-(pentafluorophenyl-amide) 74 (45 mg, 0.084 mmol) in 2 ml of anhydrous DMF under argon was stirred at 55° C. overnight. The solvent was evaporated to dryness. The residue was dissolved in 5 ml of TFA/anisole (8:2) and the mixture was kept at room temperature for 1 h. The product was precipitated by ether and purified by HPLC described in general procedure B in example 10 to give 76 (22 mg, 40%). ESI MS: 662.27 (M+H+), 331.64 (M/2+H+).

Fuente