Reacción #1654

ord-a66c33e4b2254f71b2ba86198e200a69

Ecuación de reacción

CO
methanol
Nc1ncnc2c1ncn2[C@H]1CC=CO1
product
Nc1ncnc2c1ncn2[C@H]1CC=CO1
(R)-9-(2,3-Dihydro-2-furanyl)-9H-purin-6-amine
CC(C)(C)C(=O)Cl
trimethylacetylchloride
CO.ClCCl
methylene chloride methanol
CC(C)(C)C(=O)Nc1ncnc2c1ncn2[C@H]1CC=CO1
(R)-N-[9-(2,3-Dihydro-2-furanyl)-9H-purin-6-yl]-2,2-dimethylpropanamide
Rendimiento 94.0%

Disolventes

Condiciones de reacción

Temperatura
55°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA slight 3° C. exotherm
  2. 2
    TemperaturaThe reaction solution was cooled to 25° C.
  3. 3
    Concentraciónconcentrated in vacuo to a thick orange syrup
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in methylene chloride (1.5 liters)
  5. 5
    Lavadowashed with 0.5N sodium bisulfate (3×500 mL), 1N sodium bisulfate (2×500 mL)
  6. 6
    Extracciónextracted with methylene chloride (1×500 mL)
  7. 7
    Secadodried over anhydrous sodium sulfate
  8. 8
    Filtraciónfiltered
  9. 9
    Concentraciónconcentrated in vacuo to a light orange oil
  10. 10
    Concentraciónconcentrated in vacuo

Procedimiento

To a suspension of the product of Step C (196 g, 0.97 mole), 4-dimethylaminopyridine (5.9 g, 0.048 mole) in dry pyridine (970 mL) at 26° C. was added dropwise over 1 hr trimethylacetylchloride (145 mL, 142.1 g, 1.18 mole, 1.2 equiv.). A slight 3° C. exotherm was noted. The reaction mixture was then heated to 55° C. for 4 hr becoming a pale yellow-orange solution. Analysis by TLC (methylene chloride:methanol (90:10), Rf (product) 0.75) showed the reaction was complete. The reaction solution was cooled to 25° C. and methanol (40 mL) was slowly added. The reaction solution was then stirred for 30 min, then concentrated in vacuo to a thick orange syrup. The residue was dissolved in methylene chloride (1.5 liters) and washed with 0.5N sodium bisulfate (3×500 mL), 1N sodium bisulfate (2×500 mL), then brine (1×500 mL). All aqueous washes were combined and extracted with methylene chloride (1×500 mL). All methylene chloride extracts were combined and dried over anhydrous sodium sulfate, then filtered and concentrated in vacuo to a light orange oil. The oil was suspended in toluene (200 mL) and concentrated in vacuo. The product solidified to a pale yellow solid weighing 262 g for a yield of 94%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726174uspto-grants-1998_03