Reacción #1929057

ord-1123e1cfa31346568212ddbfce7260de

Ecuación de reacción

O=C(O)c1ccc(O)cc1
4-hydroxybenzoic acid
CN(C)[P+](On1nnc2ccccc21)(N(C)C)N(C)C.F[P-](F)(F)(F)(F)F
BOP
NC(=O)c1ccc(O)cc1
4-hydroxybenzamide

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe DMF was removed by evaporation under reduced pressure
  2. 2
    workup.DISSOLUTIONdissolved by addition of aqueous sodium hydroxide solution 1M (pH 11)
  3. 3
    Otrosubjected to dialysis
  4. 4
    Otroagainst water (1 L, 2 changes over 24 h)

Procedimiento

A solution of freshly prepared 4-hydroxybenzoic acid (635 mg; 4.6 mmol) and BOP (1.7 g; 5.06 mmol) in DMF (20 mL) was added dropwise and at room temperature to a solution of PEI (1 g, 23.2 mmol) in DMF (50 mL). After 2 hours under stirring, the DMF was removed by evaporation under reduced pressure. The crude product was taken in water, dissolved by addition of aqueous sodium hydroxide solution 1M (pH 11) and subjected to dialysis using a SpectraPor 12-14 kDa membrane against water (1 L, 2 changes over 24 h). Lyophilization provided 4-hydroxybenzamide-PEI (0.7 g) at a modification degree of 28%. 1H NMR (D2O) δppm: 2.6 (bm, 2.9H, —NHCH2CH2NH—), 3.22 (m, 0.55H, Phe-CONHCH2CH2NH—), 3.35 (m, 0.55H, Phe-CONHCH2CH2NH) 6.57 (d, J=7.3 Hz, 0.55 H, CHaro), 6.97 (m, 0.55H, CHaro).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08945927B2uspto-grants-2015_02