تفاعل #171247

ord-e1342269c6c64ced828ebd7673f082dc

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزfollowed by concentration under reduced pressure
  2. 2
    workup.DISTILLATIONazeotropic distillation
  3. 3
    أخرىAfter completion of the reaction
  4. 4
    درجة الحرارةunder ice-cooling
  5. 5
    أخرىthe mixture was reacted for 20 min
  6. 6
    تركيزThe reaction mixture was concentrated under reduced pressure
  7. 7
    workup.ADDITIONWater (150 ml) was added to the concentrate
  8. 8
    استخلاصthe mixture was extracted 3 times with ethyl acetate (100 ml)
  9. 9
    تركيزThe organic layer was concentrated
  10. 10
    أخرىthe obtained oil was purified by silica gel column chromatography

الإجراء التجريبي

Suspending 2′-Deoxycytidine (2.3 g, 10.0 mmol) in dry pyridine, followed by concentration under reduced pressure was repeated 3 times to perform dehydrative azeotropic distillation, the concentrate was suspended again in dry pyridine (60 ml), and trimethylsilyl chloride (6.4 ml, 50 mmol) was added dropwise over 5 min. To the reaction mixture was added 3,5,5-trimethyl-1-hexanoyl chloride (9.5 ml, 50.0 mmol) over 5 min. After completion of the reaction, under ice-cooling, aqueous ammonia (25 ml) was added and the mixture was reacted for 20 min. The reaction mixture was concentrated under reduced pressure. Water (150 ml) was added to the concentrate, and the mixture was extracted 3 times with ethyl acetate (100 ml). The organic layer was concentrated and the obtained oil was purified by silica gel column chromatography to give the title compound (4.7 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846885B2uspto-grants-2014_09