Reacción #44649

Ecuación de reacción

((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid

HOBt

N,O-dimethylhydroxyamine hydrochloride

EDCI

N,N-diisopropylethylamine

→

titled compound

{(1R,2R)-2-benzyloxy-1-[(methoxymethylcarbamoyl)methoxymethyl]propyl}carbamic acid t-butyl ester

Disolventes

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroSolvent was removed by distillation under reduced pressure
2. 2
   workup.ADDITIONthe resultant product was diluted with ethyl acetate and water
3. 3
   OtroThe organic layer was partitioned
4. 4
   Lavadowashed with brine
5. 5
   Secadodried over anhydrous magnesium sulfate
6. 6
   OtroSolvent was removed by distillation under reduced pressure
7. 7
   Concentraciónthe filtrate was concentrated by distillation under reduced pressure

Procedimiento

To a solution of ((2R,3R)-3-benzyloxy-2-t-butoxycarbonylaminobutoxy)acetic acid (42.1 g) in DMF (400 mL) was successively added N,N-diisopropylethylamine (41 mL), N,O-dimethylhydroxyamine hydrochloride (17.4 g), EDCI (34.3 g) and HOBt (24.1 g), and the resultant solution was stirred for 16 hours at room temperature. Solvent was removed by distillation under reduced pressure, and the resultant product was diluted with ethyl acetate and water. The organic layer was partitioned, washed with brine, and then dried over anhydrous magnesium sulfate. Solvent was removed by distillation under reduced pressure. After passing the residue through a silica pad (silica gel 500 cc), the filtrate was concentrated by distillation under reduced pressure, to thereby obtain the titled compound (46.0 g). The physical properties of the compound were as follows.

Fuente