Reacción #541604

ord-97e74bbf2c854af2b0d29fb5dfe0a451

Ecuación de reacción

CCOC(=O)C1CC2(CCOCC2)CN1
ethyl 8-oxa-2-azaspiro[4.5]decane-3-carboxylate
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
COC(=O)N[C@H](C(=O)O)C(C)C
N-[(methyloxy)carbonyl]-L-valine
CCN(C(C)C)C(C)C
Hunig's base
CCOC(=O)C1CC2(CCOCC2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
product
Rendimiento 90.0%
CCOC(=O)C1CC2(CCOCC2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
ethyl 2-{N-[(methyloxy)carbonyl]-L-valyl}-8-oxa-2-azaspiro[4.5]decane-3-carboxylate
Rendimiento 90.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthe reaction was concentrated in vacuo
  2. 2
    Otropurified by C18 RP chromatography
  3. 3
    Lavadoeluting with 10-90% ACN/water/0.2% NH4OH

Procedimiento

To a solution of ethyl 8-oxa-2-azaspiro[4.5]decane-3-carboxylate (101) (200 mg, 0.94 mmol), HATU (392 mg, 1.03 mmol) and N-[(methyloxy)carbonyl]-L-valine (181 mg, 1.03 mmol) in anhydrous CH2Cl2 (6 mL) was added Hunig's base (0.33 mL, 1.88 mmol) and the solution stirred at rt under nitrogen. After 2 h, the reaction was concentrated in vacuo, purified by C18 RP chromatography, eluting with 10-90% ACN/water/0.2% NH4OH, to afford the product as a yellow oil (313 mg, 90% yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08492554B2uspto-grants-2013_07