Reaktion #50298

Reaktionsgleichung

2,4-diamino-6-hydroxypyrimidine

sodium acetate

bromoacetaldehyde diethylacetal

HCl

sodium acetate

→

2-amino-4 -hydroxy-7H-pyrrolo[2,3-d]pyrimidine

Ausbeute 79.0%

Lösungsmittel

water

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewas obtained
2. 2
   TemperaturThe solution was cooled to ambient temperature
3. 3
   workup.ADDITIONThe resulting solution was added
4. 4
   Temperaturhad been heated to 70°-85° C
5. 5
   workup.WAITto proceed for 2 hours at 70°-85° C., at which time
6. 6
   TemperaturThe mixture was cooled to 0° C.
7. 7
   workup.STIRRINGstirred for about 1.5 hours
8. 8
   FiltrationThe mixture was then filtered
9. 9
   Waschenthe collected product was washed with 500 mL of water and 500 mL of acetone
10. 10
    Sonstigedried

Vorschrift

A mixture of 136.7 g of bromoacetaldehyde diethylacetal, 347 mL of water, and 17.3 mL of concentrated HCl was heated to about 90° C. with vigorous stirring for about 30 minutes, at which time a clear solution was obtained. The solution was cooled to ambient temperature and 68.3 g of sodium acetate was added. The resulting solution was added, with stirring, to a suspension of 100 g of 2,4-diamino-6-hydroxypyrimidine and 34.2 g of sodium acetate in 739 mL of water, which had been heated to 70°-85° C. The reaction was allowed to proceed for 2 hours at 70°-85° C., at which time the reaction was complete. The mixture was cooled to 0° C. and stirred for about 1.5 hours. The mixture was then filtered and the collected product was washed with 500 mL of water and 500 mL of acetone, and dried, affording 72.3 g (79%) of 2-amino-4 -hydroxy-7H-pyrrolo[2,3-d]pyrimidine, mp>300° C. NMR δ6.03 (s, 2H), 6.13 (m, 1H), 6.56 (dd, J=3.3, 2.3 Hz, 1H), 10.23 (br s, 1H), 10.93 (br s, 1H).

Quelle