Reacción #4858

Ecuación de reacción

NMM

NMM

Racemic t-butoxycarbonyl 2,6-dimethyltyrosine

alanine methyl ester hydrochloride

→

mixture

Rendimiento 98.9%

N-[(1,1-dimethylethoxy)carbonyl]-2,6dimethyl-DL-tyrosyl-D-alanine, methyl ester

Rendimiento 98.9%

Disolventes

CH2Cl2

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturato reflux it
2. 2
   workup.ADDITION1.32 ml (10 mmoles) of IBCF were added to this stirred solution
3. 3
   Otroto rise to -15° C.
4. 4
   Otrolowered to -50° C.
5. 5
   workup.ADDITIONwas added to the solution
6. 6
   Temperaturato warm to room temperature
7. 7
   OtroThe majority of the CH2Cl2 was removed under reduced pressure
8. 8
   workup.ADDITIONEthyl acetate (200 ml) was added
9. 9
   Lavadothis solution was washed twice with 100 ml portions of 0.5 molar KHSO4, once with 100 ml of H2O
10. 10
    Secadodried over MgSO4
11. 11
    OtroRemoval of all solvent

Procedimiento

Racemic t-butoxycarbonyl 2,6-dimethyltyrosine (3.9 g, 10 mmoles) was dissolved in 30 ml of CH2Cl2 by adding 1.12 ml (10 mmoles) of NMM. After bringing this mixture to reflux it was cooled to -30° C. and 1.32 ml (10 mmoles) of IBCF were added to this stirred solution. The temperature was allowed to rise to -15° C. and then lowered to -50° C. (D) alanine methyl ester hydrochloride (1.54 g, 11 mmoles) was added to the solution followed by 1.3 ml (11 mmoles) of NMM. The mixture was allowed to warm to room temperature and stand for 16 hours. The majority of the CH2Cl2 was removed under reduced pressure. Ethyl acetate (200 ml) was added and this solution was washed twice with 100 ml portions of 0.5 molar KHSO4, once with 100 ml of H2O and dried over MgSO4. Removal of all solvent gave 3.9 g of the mixture of diastereomers. Recrystallization of this material from Skelly B/CH2Cl2 produced 1.6 g (4.2 mmoles) of diastereomer F. Removal of the solvent from the filtrate gave 1.3 g (3.3 mmoles) of diastereomer S contaminated by less than 10% of diastereomer F.

Fuente