Reaktion #640642

ord-081afe95e6734940bcb30313933b840c

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe mixture was stirred for 4 h at room temperature
  2. 2
    SonstigeThe solid that formed in the mixture
  3. 3
    Sonstigewas removed by filtration
  4. 4
    Waschenwashed with EtOAc
  5. 5
    Waschenwashed with 1N HCl and saturated aqueous NaHCO3
  6. 6
    TrocknenThe organic layer was dried over Na2SO4
  7. 7
    Filtrationfiltered
  8. 8
    Einengenconcentrated

Vorschrift

A solution of 3-tert-butoxycarbonylaminopropanoic acid (2 g, 10.6 mmol.) and HOSu (1.22 g, 10.6 mmol.) in 40 mL DCM/Dioxane (2:1) was cooled in an ice bath. To this solution was added DCC (2.4 g, 11.6 mmol.), and the mixture was stirred at room temperature for 1 h. To the resulting mixture was added benzylamine (1.7 g, 15.8 mmol.), the mixture was stirred for 4 h at room temperature. The solid that formed in the mixture was removed by filtration and washed with EtOAc. The filtrate and washings were combined and washed with 1N HCl and saturated aqueous NaHCO3. The organic layer was dried over Na2SO4, filtered and concentrated to afford 3-tert-butoxycarbonylamino-N-benzylpropionamide (2.4 g, 82%). 3-tert-Butoxycarbonylamino-N-benzylpropionamide was dissolved in cooled HCl/MeOH (20 mL) and the resulting mixture was stirred at room temperature for 1.5 h. The solvent was removed to afford 3-amino-N-benzylpropionamide hydrochloride (1.8 g, 100%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08048862B2uspto-grants-2011_11