Hydrochloric Acid → 4-(1-Methyl-2,6-dioxo-1,2,6,7-tetrahydro-3H-purin-3-yl)butanoic acid

HRID 904273Notes

Reaction equation

HRID 904273 reaction equation
[CH3:1][N:2]1[C:11](=[O:12])[C:10]2[N:9](COC(=O)C(C)(C)C)[CH:8]=[N:7][C:6]=2[N:5]([CH2:21][CH2:22][CH2:23][C:24]([O:26]CC)=[O:25])[C:3]1=[O:4].Cl>[OH-].[Na+]>[CH3:1][N:2]1[C:11](=[O:12])[C:10]2[NH:9][CH:8]=[N:7][C:6]=2[N:5]([CH2:21][CH2:22][CH2:23][C:24]([OH:26])=[O:25])[C:3]1=[O:4]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 128798421-Methyl-3(carboethoxypropyl)-7-(pivaloyloxymethyl)xanthine

Product 1

HCID 128798434-(1-Methyl-2,6-dioxo-1,2,6,7-tetrahydro-3H-purin-3-yl)butanoic acid

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

An oily suspension of 1-methyl-3-(carboethoxypropyl)-7-(pivaloyloxymethyl)xanthine (508 mg) in 2N NaOH(36.2 ml) was heated under nitrogen at 95°-100° for 2 hrs. The oil dissolved and the reaction was shown to be complete by TLC. After cooling the reaction mixture, it was acidified to pH 2-3 with 15 ml 12% hydrochloric acid and the solution extracted with 3×5 ml chloroform to remove the pivalic acid. After washing the chloroform extracts with 5 ml 0.5 N HCl, the aqueous solutions were combined and stripped to dryness and the residue dried in vacuo at room temperature. The crude product was dissolved in about 22 ml hot water, decolorized and concentrated to 15 ml, at which time 159 mg of a crystalline product was obtained upon cooling. m.p. 220°-221°.

Workup

  1. temperaturewas heated under nitrogen at 95°-100° for 2 hrs
  2. dissolutionThe oil dissolved
  3. temperatureAfter cooling the reaction mixture, it
  4. extractionthe solution extracted with 3×5 ml chloroform
  5. customto remove the pivalic acid
  6. washAfter washing the chloroform
  7. customthe residue dried in vacuo at room temperature
  8. dissolutionThe crude product was dissolved in about 22 ml hot water
  9. concentrationdecolorized and concentrated to 15 ml, at which time 159 mg of a crystalline product
  10. customwas obtained
  11. temperatureupon cooling

Sources & evidence

ORD record
ord-638a4301c1e3489c9170b04d3c9d5f85
Source dataset
uspto-grants-1980_10
Patent number
US04230805

Reaction notes

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