Reacción #64855

Ecuación de reacción

BOC-L-Ala

serinol hydrochloride

N-methylmorpholine

HOBT

H2O

1,3-dicyclohexylcarbodiimide

→

crude product

BOC-L-Ala-SerOH

Disolventes

acetic acid

DMF

CH2Cl2

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONtreated dropwise with a solution that
2. 2
   workup.STIRRINGThe reaction mixture was stirred at RT for 20 hours
3. 3
   workup.STIRRINGstirred for another hour
4. 4
   OtroThe solid reaction by-products
5. 5
   Otrowere removed by filtration
6. 6
   Lavadowashed with 20 ml CH2Cl2
7. 7
   ConcentraciónThe combined filtrate and washings was concentrated to dryness on the rotary evaporator
8. 8
   Otrothen further dried under high vacuum
9. 9
   Temperaturacooled at 4° C. for several hours
10. 10
    Filtraciónfiltered
11. 11
    ConcentraciónThe filtrate was concentrated to dryness on the rotary evaporator
12. 12
    Otrofurther dried under high vacuum

Procedimiento

BOC-L-Ala (567 mg, 2 mMol) and HOBT.H2O (505 mg, 3.3 mMol) were dissolved in 5 ml CH2Cl2 and 5 ml DMF, then treated with 1,3-dicyclohexylcarbodiimide (DCC, 680 mg, 3.3 mMol). The resulting solution was stirred at RT for one hour, then treated dropwise with a solution that contained 421 mg (3.3 mMol) of serinol hydrochloride (Aldrich) and 333 mg (3.3 mMol) of N-methylmorpholine in 5 ml of DMF. The reaction mixture was stirred at RT for 20 hours, then treated with 0.5 ml of glacial acetic acid and stirred for another hour. The solid reaction by-products were removed by filtration and washed with 20 ml CH2Cl2. The combined filtrate and washings was concentrated to dryness on the rotary evaporator then further dried under high vacuum. The oily residue was taken up in 50 ml of H2O, cooled at 4° C. for several hours, then filtered. The filtrate was concentrated to dryness on the rotary evaporator, then further dried under high vacuum to yield the crude product as a yellow oil.

Fuente