Reacción #428200

ord-9c2dd8b544be4a40b40514c2ca140f89

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto quench
  2. 2
    Otrothe reaction
  3. 3
    OtroThe solvents were removed
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in EtOAc (100 mL)
  5. 5
    FiltraciónThe salt was filtered off
  6. 6
    Concentraciónthe filtrate was concentrated

Procedimiento

To a solution of (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate (4.2 g, 6.8 mmol, 1.0 equiv.) in MeOH (35 mL), was added HCl (2N, 0.68 mL, 1.36 mmol, 0.2 equiv.). The reaction was stirred at RT for 1 h. NaHCO3 (1.1 g, 13.6 mmol, 2.0 equiv) was added to quench the reaction. The solvents were removed. The residue was dissolved in EtOAc (100 mL). The salt was filtered off and the filtrate was concentrated to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoyl)piperazine-1-carboxylate (3.4 g, quant.). LRMS (M+H+) m/z 501.2.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08895582B2uspto-grants-2014_11