Hydrochloric Acid → HCID 178508865, compound

HRID 22020

Reaction equation

HRID 22020 reaction equation
[CH2:1](OC(OCC)CBr)[CH3:2].Cl.C([O-])(=O)C.[Na+].[NH2:16][C:17]1[N:22]=[C:21]([NH2:23])[CH:20]=[C:19]([OH:24])[N:18]=1>O>[NH2:16][C:17]1[N:18]=[C:19]([OH:24])[C:20]2[CH:2]=[CH:1][NH:23][C:21]=2[N:22]=1

Participants

6

Conditions

Temperature
90 °C

Procedure

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).

Workup

  1. customwas obtained
  2. temperatureThe solution was cooled to ambient temperature
  3. additionThe resulting solution was added
  4. temperaturehad been heated to 70°-85° C
  5. waitto proceed for 2 hours at 70°-85° C., at which time
  6. temperatureThe mixture was cooled to 0° C.
  7. stirringstirred for about 1.5 hours
  8. filtrationThe mixture was then filtered
  9. washthe collected product was washed with 500 mL of water and 500 mL of acetone
  10. customdried

Sources & evidence

ORD record
ord-dfede456fd9e4c148ee79d0562641559
Source dataset
uspto-grants-1995_06
Patent number
US05426187

Linked notes

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