Reacción #1271

Ecuación de reacción

formaldehyde

amine

Nα-CBZ-O-t-butyl L-lysine

NaCNBH3

→

Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine

Disolventes

methanol

methanol

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrowas prepared to which
2. 2
   TemperaturaAfter cooling to 10°-15° C
3. 3
   Lavadomonitored by silica gel TLC with elution
4. 4
   workup.ADDITION1(v/v/v/) mixture of chloroform/methanol/concentrated ammonia (solvent A)
5. 5
   workup.ADDITIONOne hundred milliliters of water was added
6. 6
   Concentraciónthe mixture concentrated to a volume of 200 ml
7. 7
   workup.ADDITIONEthyl acetate (200 mL) was added
8. 8
   Temperaturathe pH raised to 10.5 with 10% NaOH
9. 9
   OtroThe ethyl acetate was separated
10. 10
    Extracciónextracted with 200 mL of fresh ethyl acetate
11. 11
    Lavadowashed with NaCl
12. 12
    Secadodried over Na2SO4
13. 13
    Filtraciónfiltered
14. 14
    Concentraciónconcentrated
15. 15
    Otroto yield
16. 16
    Secadoafter drying overnight under high vacuum, 14.86 g of viscous oil

Procedimiento

A mixture consisting of 3.7 (27.2 mmol) of ZnCl2, 3.2 g (53 mmol) of NaCNBH3 and 60 mL of methanol was prepared to which was added a solution of 18 g (51.7 mmol) of the amine 1 in 180 mL of methanol. After cooling to 10°-15° C. 12.4 mL of 37% formaldehyde (165 mmol) was added dropwise over a 2-3 minute period. The reaction was stirred for 1 hour and monitored by silica gel TLC with elution using a 60:10:1(v/v/v/) mixture of chloroform/methanol/concentrated ammonia (solvent A). One hundred milliliters of water was added and the mixture concentrated to a volume of 200 ml. Ethyl acetate (200 mL) was added and the pH raised to 10.5 with 10% NaOH. The ethyl acetate was separated and the pH of the aqueous phase readjusted to 10.5 and extracted with 200 mL of fresh ethyl acetate. The ethyl acetate extracts were combined, washed with NaCl, dried over Na2SO4, filtered and concentrated to yield, after drying overnight under high vacuum, 14.86 g of viscous oil.

Fuente