Reacción #2122526

ord-72650a73f86e40fd972b5647e64084b9

Ecuación de reacción

CC=O
acetaldehyde
CC(C)(C)OC(=O)N[C@@H](CCN)C(=O)O
(S)-4-amino-2-(tert-butoxycarbonylamino) butanoic acid
CO.O
water MeOH
[BH3-]C#N.[Na+]
NaCNBH3
CC=O
acetaldehyde
CCN(CC)CC[C@H](N)C(=O)O
(S)-2-amino-4-(diethylamino)butanoic acid

Condiciones de reacción

Temperatura
40°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe cooling bath was removed
  2. 2
    workup.STIRRINGthe reaction was stirred for 20.5 hr
  3. 3
    OtroMost of the MeOH component was removed in vacuo
  4. 4
    workup.ADDITIONthe remaining mixture was treated with concentrated HCl until its pH
  5. 5
    OtroThe volatile component was removed in vacuo
  6. 6
    workup.ADDITIONthe residue was treated with 4 M HCl/dioxane (20 mL)
  7. 7
    workup.STIRRINGstirred at ambient condition for 7.5 hr
  8. 8
    OtroThe volatile component was removed in vacuo
  9. 9
    Otrothe residue was purified with Dowex ® 50WX8-100 ion-exchange resin (column
  10. 10
    Lavadowas washed with water
  11. 11
    Lavadothe compound was eluted with dilute NH4OH
  12. 12
    Otroprepared from 18 ml of NH4OH and 282 ml of water)

Procedimiento

NaCNBH3 (1.60 g, 24.2 mmol) was added in batches to a chilled (˜15° C.) water/MeOH (12 mL each) solution of (S)-4-amino-2-(tert-butoxycarbonylamino) butanoic acid (2.17 g, 9.94 mmol). A few minutes later acetaldehyde (2.7 mL, 48.1 mmol) was added drop-wise over 2 min, the cooling bath was removed, and the reaction mixture was stirred at ambient condition for 3.5 hr. An additional acetaldehyde (2.7 mL, 48.1 mmol) was added and the reaction was stirred for 20.5 hr. Most of the MeOH component was removed in vacuo, and the remaining mixture was treated with concentrated HCl until its pH reached ˜1.0 and then heated for 2 hr at 40° C. The volatile component was removed in vacuo, and the residue was treated with 4 M HCl/dioxane (20 mL) and stirred at ambient condition for 7.5 hr. The volatile component was removed in vacuo and the residue was purified with Dowex ® 50WX8-100 ion-exchange resin (column was washed with water and the compound was eluted with dilute NH4OH, prepared from 18 ml of NH4OH and 282 ml of water) to afford intermediate (S)-2-amino-4-(diethylamino)butanoic acid as an off-white solid (1.73 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08574563B2uspto-grants-2013_11