تفاعل #58780

ord-82096f8f3d144aaebd4748ff49216b99

معادلة التفاعل

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
adenosine
COC(C)(C)OC
2,2-dimethoxypropane
CC(C)=O
acetone
CC1(C)OC2C(CO)OC(n3cnc4c(N)ncnc43)C2O1
2′,3′-Isopropylidene-adenosine

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe resulting reaction
  2. 2
    تركيزThe reaction mixture was concentrated in vacuo
  3. 3
    workup.ADDITIONdiluted with a mixture of saturated aqueous NaHCO3 (250 mL) and ethyl acetate (250 mL)
  4. 4
    أخرىThe resulting solution was transferred to a separatory funnel
  5. 5
    أخرىthe organic layer was separated
  6. 6
    تجفيفdried over sodium sulfate
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىto provide a solid residue
  9. 9
    ترشيحfiltered
  10. 10
    غسيلwashed with hexane
  11. 11
    أخرىdried

الإجراء التجريبي

A solution of adenosine (43 g) and 2,2-dimethoxypropane (5 eq.) in acetone (75 eq.) was treated with D-camphorsulphonic acid (1 eq) at and the resulting reaction was allowed to stir for 3 hr. The reaction mixture was concentrated in vacuo and diluted with a mixture of saturated aqueous NaHCO3 (250 mL) and ethyl acetate (250 mL). The resulting solution was transferred to a separatory funnel and the organic layer was separated, dried over sodium sulfate, and concentrated in vacuo to provide a solid residue. The solid residue was suspended in hexane, filtered, washed with hexane and dried to provide 2′,3′-Isopropylidene-adenosine (43 g). 1H NMR (DMSO-d6, 300 MHz): δ 4.12-4.17 (m, 1H), 4.22-4.26 (m, 1H), 4.59 (d, J=4.8 Hz, 1H), 4.74-4.85 (m, 2H), 5.49-5.52 (m, 1H), 5.51 (d, J=5.1 Hz, 1H), 5.84 (d, J=5.1 Hz, 1H), 7.85 (s, 2H), 8.33 (s, 1H). MS m/z 347.11 [M+H]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07423144B2uspto-grants-2008_09