Reaktion #79452

Reaktionsgleichung

N4-benzyloxycarbonyl-cytosine

potassium carbonate

Sodium carbonate

4-nitrophenol

→

title compound

tert-Butyl 4-nitrophenyl Carbonate

Lösungsmittel

DMF

dioxane

dioxane

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe mixture was refluxed for 1 h
2. 2
   Filtrationfiltered
3. 3
   Einengenconcentrated
4. 4
   workup.ADDITIONpoured into wat
5. 5
   Filtrationfiltered
6. 6
   Sonstigeevaporated to dryness, in vacuo
7. 7
   workup.ADDITIONWater (300 ml) and 4 N hydrochloric acid (10 ml) were added
8. 8
   workup.STIRRINGthe mixture was stirred for 15 minutes at 0° C.
9. 9
   Filtrationfiltered
10. 10
    Waschenwashed with water (2×75 ml)
11. 11
    workup.ADDITIONThe isolated precipitate was treated with water (120 ml), 2N sodium hydroxide (60 ml)
12. 12
    workup.STIRRINGstirred for 30 min
13. 13
    Filtrationfiltered
14. 14
    Temperaturcooled to 0° C.
15. 15
    workup.ADDITION4 N hydrochloric acid (35 ml) was added

Vorschrift

Sodium carbonate (29.14 g; 0.275 mol) and 4-nitrophenol (12.75 g; 91.6 mmol) were mixed with dioxane (250 ml). Boc-anhydride (20.0 g; 91.6 mmol) was transferred to the mixture with dioxane (50 ml). The mixture was refluxed for 1 h, cooled to 0° C., filtered and concentrated to ⅓, and then poured into wat.82 ml;82.6 mmol) and a suspension of N4-benzyloxycarbonyl-cytosine (9, 21.0 g;82.6 mmol) and potassium carbonate (11.4 g;82.6 mmol) in dry DMF (900 ml). The mixture was stirred vigorously overnight, filtered, and evaporated to dryness, in vacuo. Water (300 ml) and 4 N hydrochloric acid (10 ml) were added, the mixture was stirred for 15 minutes at 0° C., filtered, and washed with water (2×75 ml). The isolated precipitate was treated with water (120 ml), 2N sodium hydroxide (60 ml), stirred for 30 min, filtered, cooled to 0° C., and 4 N hydrochloric acid (35 ml) was added. The title compound was isolated by filtration, washed thoroughly with water, recrystallized from methanol (1000 ml) and washed thoroughly with ether. This afforded 7.70 g (31%) of pure compound. The mother liquor from the recrystallization was reduced to a volume of 200 ml and cooled to 0° C. This afforded an additional 2.30 g of a material that was pure by tlc but had a reddish color. M.p. 266-274° C. Anal., for C14H13N3O5. Found(calc.); C, 55.41(55.45); H, 4.23(4.32); N, 14.04(13.86) 1H-NMR (90 MHz; DMSO-d6): 8.02 ppm (d,J=7.32 Hz,1H,H-6); 7.39 (s,5H,Ph); 7.01 (d,J=7.32 Hz,1H,H-5); 5.19 (s,2H,PhCH2—); 4.52. (s,2H).

Quelle