Reacción #1552038

ord-9afacb27f2cf49fc8f591ed72138b011

Ecuación de reacción

Cl
hydrochloric acid
CCCCCCCCCCCCCCCC(=O)ON1C(=O)CCC1=O
N-palmitoyloxy-succinimide
NCC(=O)O
Gly
CCN(CC)CC
triethylamine
CCCCCCCCCCCCCCCC(=O)NCC(=O)O
desired compound
Rendimiento 67.0%
CCCCCCCCCCCCCCCC(=O)NCC(=O)O
N-palmitoyl-Gly
Rendimiento 67.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawhile cooled with ice
  2. 2
    workup.ADDITIONwere added dropwise
  3. 3
    OtroTo an aqueous solution obtained
  4. 4
    Temperaturawhile cooled with ice
  5. 5
    workup.STIRRINGwith stirring
  6. 6
    workup.ADDITIONthe reaction solution was added dropwise
  7. 7
    Otroto precipitate a solid, which
  8. 8
    Filtraciónwas filtered off
  9. 9
    LavadoThe resultant product was washed with 2 L of water
  10. 10
    Otrowith 1 L of hexane, and was then collected

Procedimiento

260.3 g of the N-palmitoyloxy-succinimide synthesized above as a whole was suspended in 750 ml of DMF and, to the resultant solution while cooled with ice with stirring, 56.3 g (0.750 mol) of Gly and 83.2 mL (0.598 mol) of triethylamine dissolved in 250 ml of water were added dropwise. The resultant solution was stirred for another 30 minutes while cooled with ice and for another 15 hours during which the resultant solution gradually reached room temperature. To an aqueous solution obtained by dissolving 100 mL of 6 N hydrochloric acid in 1 L of water and adjusting the pH to pH 3, while cooled with ice with stirring, the reaction solution was added dropwise to precipitate a solid, which was filtered off. The resultant product was washed with 2 L of water and then with 1 L of hexane, and was then collected to obtain 114 g (67%) of a desired compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08999300B2uspto-grants-2015_04