2H-Purine-2-thione, 6-amino-3,7-dihydro- → HCID 178420864, compound

HRID 2227353Notes

Reaction equation

HRID 2227353 reaction equation
[NH:1]1[C:10](N)=[C:9]2[C:5]([N:6]=[CH:7][NH:8]2)=[N:4][C:2]1=S>C(O)CC.[Ni]>[N:1]1[CH:10]=[C:9]2[C:5](=[N:6][CH:7]=[N:8]2)[NH:4][CH:2]=1

Participants

4

Reactant 1

HCID 15020112H-Purine-2-thione, 6-amino-3,7-dihydro-

Product 1

HCID 178420864HCID 178420864, compoundYield 140.8%

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 10311-PropanolSolvent

Procedure

4.39 g (11 mmoles) of thioisoguanine and 7.10 g (121 mmoles) of neutral Raney-nickel are refluxed in 50 ml of 1-propanol for 4.5 hours. The nickel was filtered off and the filtrate evaporated to dryness. The residue (3.79 g/93.8%) was dissolved in 20 ml of chloroform and 0.4 ml methanol and filtered through 24 g of silicagel in a column also with 2% methanol. The combined fractions were washed with 1N NaOH and the organic phase evaporated to dryness. The residue (2.69 g/66.6%) was dissolved in 30 ml of dichloromethane and 0.6 ml methanol and again filtered through 30 g of silicagel. A total of 1.86 g (46.0%) of 3H-purine was isolated, which was dissolved in 20 ml of methanol, treated with 5.4 ml of 1N methanolic HCl, and evaporated in vacuo to dryness. Crystallization and recrystallization from dichloromethane and ethyl acetate gave 1.75 g (39.4%) of 3H-purine hydrochloride with mp 170-85° C.

Workup

  1. filtrationThe nickel was filtered off
  2. customthe filtrate evaporated to dryness
  3. dissolutionThe residue (3.79 g/93.8%) was dissolved in 20 ml of chloroform
  4. filtration0.4 ml methanol and filtered through 24 g of silicagel in a column also with 2% methanol
  5. washThe combined fractions were washed with 1N NaOH
  6. customthe organic phase evaporated to dryness
  7. dissolutionThe residue (2.69 g/66.6%) was dissolved in 30 ml of dichloromethane
  8. filtration0.6 ml methanol and again filtered through 30 g of silicagel

Sources & evidence

ORD record
ord-f2a342afe59d4507a86fe8a88f2d344b
Source dataset
uspto-grants-2002_07
Patent number
US06413975B1

Reaction notes

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