Reacción #2175468

ord-96c420f0b2704609aa8ed116c9802a80

Ecuación de reacción

CS(=O)(=O)O
Methanesulfonic acid
C[C@H](COC(=O)[C@H](Cc1ccc(O)c(O)c1)NC(=O)OC(C)(C)C)OC(=O)c1ccccc1
(2R)-2-phenylcarbonyloxypropyl (2S)-2-(tert-butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoate
COC(C)(C)C
methyl tert-butyl ether
CS(=O)(=O)O.C[C@H](COC(=O)[C@@H](N)Cc1ccc(O)c(O)c1)OC(=O)c1ccccc1
mesylate salt
Rendimiento 54.4%
CS(=O)(=O)O.C[C@H](COC(=O)[C@@H](N)Cc1ccc(O)c(O)c1)OC(=O)c1ccccc1
(2R)-2-Phenylcarbonyloxypropyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate mesylate
Rendimiento 54.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe mixture was stirred for 2 h
  2. 2
    FiltraciónThe resulting suspension was filtered
  3. 3
    LavadoThe filter cake was washed three times with methyl tort-butyl ether and air
  4. 4
    Otrodried

Procedimiento

Methanesulfonic acid (3.9 mL, 60.1 mmol) was slowly added to a solution of (2R)-2-phenylcarbonyloxypropyl (2S)-2-(tert-butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoate 1e (11.0 g, 22.1 mmol) in 1,4-dioxane (30 mL) while stirred at room temperature. The mixture was stirred for 2 h. The solution was slowly added to methyl tert-butyl ether (MTBE) (600 mL) with vigorous stirring. The resulting suspension was filtered. The filter cake was washed three times with methyl tort-butyl ether and air dried to afford 5.48 g (54% yield) of anhydrous mesylate salt 1 as an off-white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08435562B2uspto-grants-2013_05