Reaction #335505

Reaction equation

4-methoxy-1-phenylethylamine

N-methylpiperidine

t-butoxycarbonyl-L-valine

isobutyl chloroformate

→

N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide

Solvents

CH2Cl2

Conditions

Workup

1. 1
   Otherbeing kept below -15° C
2. 2
   workup.WAITAfter 2 hours at -15° C.
3. 3
   workup.STIRRINGthe mixture is subsequently stirred at room temperature for 15 hours
4. 4
   Filtrationthe solid is filtered off
5. 5
   Washrinsed with CH2Cl2
6. 6
   Concentrationthe filtrate is concentrated
7. 7
   workup.ADDITIONthe residue is introduced into water
8. 8
   Extractionthe mixture is extracted twice with ethyl acetate
9. 9
   Washthe combined ethyl acetate phases are washed with NaHCO3 solution and water
10. 10
    Otherdried
11. 11
    Concentrationconcentrated

Procedure

2.3 g (0.023 mol) of N-methylpiperidine are added to 5.0 g of t-butoxycarbonyl-L-valine (0.023 mol), dissolved in 50 ml of CH2Cl2, at -20° C. 3.2 g (0.023 mol) of isobutyl chloroformate are then rapidly added dropwise at -20° C., the mixture is subsequently stirred at the same temperature for 10 minutes and cooled to -60° C. and 3.5 g (0.023 mol) of 4-methoxy-1-phenylethylamine are allowed to run in, the temperature being kept below -15° C. After 2 hours at -15° C., the mixture is subsequently stirred at room temperature for 15 hours, the solid is filtered off and rinsed with CH2Cl2, the filtrate is concentrated, the residue is introduced into water, the mixture is extracted twice with ethyl acetate and the combined ethyl acetate phases are washed with NaHCO3 solution and water, dried and concentrated. 17.5 g (85% of theory) of N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide of melting point 126°-127° C. are obtained.

Source