Reacción #313640

Ecuación de reacción

HOBt

(2R)-2-[(tert-butoxycarbonyl)amino]-4-(methylthio)butanoic acid

cyclohexanemethylamine

EDCI

→

tert-butyl [(1R)-1-{[(cyclohexylmethyl)amino]carbonyl}-3-(methylthio)propyl]carbamate

Rendimiento 89.5%

Disolventes

AcOEt-H2O

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   Lavadothe organic layer was washed with aqueous ammonium chloride, aqueous sodium hydrogen carbonate, and brine
2. 2
   Secadodried over MgSO4
3. 3
   OtroThe solvent was evaporated in vacuo
4. 4
   Otrothe residue was crystallized from ethyl acetate and hexane

Procedimiento

A mixture of (2R)-2-[(tert-butoxycarbonyl)amino]-4-(methylthio)butanoic acid (4.57 g), cyclohexanemethylamine (2.28 g), HOBt (2.72 g), and EDCI (3.87 g) in DMF (50 mL) was stirred at ambient temperature for 15 hours. The reaction mixture was poured into a mixture of AcOEt-H2O and the organic layer was washed with aqueous ammonium chloride, aqueous sodium hydrogen carbonate, and brine and dried over MgSO4. The solvent was evaporated in vacuo and the residue was crystallized from ethyl acetate and hexane to give tert-butyl [(1R)-1-{[(cyclohexylmethyl)amino]carbonyl}-3-(methylthio)propyl]carbamate (5.65 g).

Fuente