Water → HCID 178508925, compound

HRID 1761235Notes

Reaction equation

HRID 1761235 reaction equation
C([O:4][CH2:5][CH:6]([CH2:20][O:21]C(=O)C)[CH2:7][CH2:8][N:9]1[CH:17]=[N:16][C:15]2[C:10]1=[N:11][C:12]([NH2:19])=[N:13][C:14]=2Cl)(=O)C.[OH2:25].[OH-].[Na+]>C(O)=O>[OH:4][CH2:5][CH:6]([CH2:20][OH:21])[CH2:7][CH2:8][N:9]1[CH:17]=[N:16][C:15]2[C:14](=[O:25])[NH:13][C:12]([NH2:19])=[N:11][C:10]1=2.[CH:17]1[N:9]([CH2:8][CH2:7][CH:6]([CH2:20][OH:21])[CH2:5][OH:4])[C:10]2[N:11]=[C:12]([NH2:19])[N:13]=[C:14]([OH:25])[C:15]=2[N:16]=1

Participants

5

Conditions

Temperature
42.5 °C

Procedure

A mixture of 9-(4-acetoxy-3-acetoxymethylbut-1-yl)-2-amino-6-chloropurine (10 g, 28.1 mmole), formic acid (96%. 6.3 ml) and water (55 ml) was stirred and heated to reflux for about 4 hours. After cooling the solution was basified by mixing with sodium hydroxide solution (12.5M, 27 ml) and the resulting solution was stirred for 1.5 hrs. The solution was neutralised by the addition of formic acid. The resultant slurry was heated to reflux (ca 105° C.) then cooled to 40-45° C. and stirred for about 3 hours. The crude product is then isolated and washed with water (20 ml). The isolated product was dissolved in sodium hydroxide solution (3M, 80 ml). Carbon (ca 1.5 g) was added and the slurry stirred for about 1 hr then the carbon was removed by filtration and washed with water (20 ml). The solution was neutralised by the addition of formic acid and the resultant precipitate was redissolved by heating to ca 100° C. and was then cooled. The precipitated product was stirred for about 3 hrs then isolated and washed with water (2×20 ml) before being dried.

Workup

  1. temperatureheated
  2. temperatureto reflux for about 4 hours
  3. temperatureAfter cooling the solution
  4. stirringthe resulting solution was stirred for 1.5 hrs
  5. temperatureThe resultant slurry was heated
  6. temperatureto reflux (ca 105° C.)
  7. stirringstirred for about 3 hours

Sources & evidence

ORD record
ord-c5149472863c4681aff50f29e86d2eaf
Source dataset
uspto-grants-2005_01
Patent number
US06846927B1

Reaction notes

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