Reacción #2175517

ord-f7e788e5d2674ba3900d40327732133a

Ecuación de reacción

CCOC(=O)C(N)CCC(=O)NC(CO)C(=O)OCC
alcohol
CCOC(=O)C(N)CCC(=O)NC(CO)C(=O)OCC
2-amino-4-(1-ethoxycarbonyl-2-hydroxy-ethylcarbamoyl)-butyric acid ethyl ester
O=S(Cl)Cl
thionyl chloride
CCOC(=O)C([NH3+])CCC(=O)NC(CCl)C(=O)OCC.[Cl-]
3-(2-chloro-1-ethoxycarbonyl-ethylcarbamoyl)-1-ethoxycarbonyl-propyl-ammonium chloride
Rendimiento 84.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was removed on a rotary evaporator (bath temperature below 28° C.)
  2. 2
    workup.ADDITIONDichloromethane (100 ml) was added
  3. 3
    OtroThe solid residue was triturated with DCM (100 mL), Heptane (100 mL), and MTBE (100 ml)
  4. 4
    Otroto give 10 g (84% yield) of pure 6 (LCMS) as a off-white solid

Procedimiento

A solution of alcohol 5 (10 g, 35 mmol) in dichloromethane (350 ml) was treated with thionyl chloride (20 mL) and stirred at room temperature under nitrogen overnight. The solvent was removed on a rotary evaporator (bath temperature below 28° C.). Dichloromethane (100 ml) was added and stripped under the same conditions twice. The solid residue was triturated with DCM (100 mL), Heptane (100 mL), and MTBE (100 ml) to give 10 g (84% yield) of pure 6 (LCMS) as a off-white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08435956B2uspto-grants-2013_05