Reacción #497063

ord-6179cc1b1cdc4a15ac08fb4069a591d1

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: US08759374B2uspto-grants-2014_06