Reacción #76837

ord-fd5c64ed8b2a4ec8b5c23cabdd62366f

Ecuación de reacción

CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)O
N-Boc-L-valine
C(=NC1CCCCC1)=NC1CCCCC1
N,N′-dicyclohexyl carbodiimide
CCCCCCCCCCCCCCCCCC(=O)OCC[C@@H](CO)Cn1cnc2c(=O)[nH]c(N)nc21
(R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine
CN(C)C=O
N,N-dimethylformamide
CCCCCCCCCCCCCCCCCC(=O)OCC[C@@H](COC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)Cn1cnc2c(=O)[nH]c(N)nc21
pure title compound
Rendimiento 39.3%
CCCCCCCCCCCCCCCCCC(=O)OCC[C@@H](COC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)Cn1cnc2c(=O)[nH]c(N)nc21
(R)-9-[2-(N-Boc-L-valyloxymethyl)-4-(stearoyloxy)butyl]guanine
Rendimiento 39.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtracióndicyclohexylurea filtered off
  2. 2
    Extracciónextracted with a small volume of dichloromethane
  3. 3
    Otrothe filtrate evaporated in vacuo to a small volume
  4. 4
    workup.STIRRINGthe mixture was stirred for 4 h at 50° C. under N2
  5. 5
    OtroThe solvent was evaporated in vacuo to a small volume

Procedimiento

A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mg) in dichloromethane (20 ml) was stirred over night at room temperature, dicyclohexylurea filtered off and extracted with a small volume of dichloromethane, and the filtrate evaporated in vacuo to a small volume. (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine (340 mg; 0.654 mmol), 4-dimethylaminopyridine (25 mg; 0.205 mmol), and dry N,N-dimethylformamide (15 ml) were added and the mixture was stirred for 4 h at 50° C. under N2. The solvent was evaporated in vacuo to a small volume. Column chromatography on silica gel, then on aluminum oxide (ethyl acetate:methanol: water 15:2:1 as eluent) gave 185 mg (39%) pure title compound as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06703394B2uspto-grants-2004_03