Reacción #806269

ord-9c4385e7af3d4410a697e93018c48d2e

Ecuación de reacción

CC[NH+](CC)CC.CC[NH+](CC)CC.N#CCCCCC#Cc1nc(N)c2ncn([C@@H]3O[C@H](COP(=O)([O-])[O-])[C@@H](O)[C@H]3O)c2n1
triethylammonium 2-(6-cyano-1-hexyn-1-yl)adenosine 5′-monophosphate
Cl
HCl
N#CCCCCC#Cc1nc(N)c2ncn([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)c2n1
2-(6-cyano-1-hexyn-1-yl)adenosine 5′-monophosphate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    Filtraciónthe resultant mixture was filtered
  3. 3
    LavadoThe residue was washed with water (20 mL)

Procedimiento

A triethylammonium 2-(6-cyano-1-hexyn-1-yl)adenosine 5′-monophosphate (1.1 g) was dissolved in water (20 mL), and, under ice-cooling conditions, 1N HCl solution (2 mL) was added thereto, followed by standing for 10 minutes. After having been diluted with water (20 mL), the resultant mixture was filtered. The residue was washed with water (20 mL) and then with ethanol (20 mL×2), to thereby yield 617 mg of the above-titled compound as a colorless amorphous substance.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07132409B2uspto-grants-2006_11