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Chemical Structure| 82448-39-3 Chemical Structure| 82448-39-3

Structure of 82448-39-3

Chemical Structure| 82448-39-3

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Product Details of [ 82448-39-3 ]

CAS No. :82448-39-3
Formula : C7H8N4O2
M.W : 180.16
SMILES Code : O=C(N1)N(C)C2=C(NC(C)=N2)C1=O

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Application In Synthesis of [ 82448-39-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 82448-39-3 ]

[ 82448-39-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6972-82-3 ]
  • [ 82448-39-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In sodium hydroxide; acetic anhydride; A solution of <strong>[6972-82-3]5,6-diamino-1-methyluracil</strong> (2.5 g) in acetic anhydride (25 ml) was heated at reflux for 2 hours and then the acetic anhydride was evaporated under reduced pressure. The residue was dissolved in 10 percent aqueous sodium hydroxide solution (50 ml) and heated at reflux for 2 hours. After cooling to room temperature, the mixture was acidified to pH 4 by addition of concentrated hydrochloric acid. The precipitate was filtered, washed with water (15 ml), rinsed with acetone (15 ml) and dried under vacuum to provide 3,8-dimethylxanthine (1.8 g).
In sodium hydroxide; acetic anhydride; B. Preparation of 3,8-Dimethylxanthine A solution of 1-methyl-5,6-diaminouracil (2.5 g) in acetic anhydride (25 ml) was heated at reflux for 2 hours and then concentrated. The residue was dissolved in 10percent sodium hydroxide solution (50 ml) and heated at reflux for 2 hours. After cooling to room temperature the solution was acidified to pH 4 with concentrated hydrochloric acid. The product was filtered, washed with water (15 ml), with acetone (15 ml) and then dried under vacuum. Yield 1.8 g.
With concentrated hydrochloric acid; In aqueous sodium hydroxide; acetic anhydride; A solution of <strong>[6972-82-3]5,6-diamino-1-methyluracil</strong> (2.5 g) in acetic anhydride (25 ml) was heated at reflux for 2 hours and then the acetic anhydride was evaporated under reduced pressure. The residue was dissolved in 10percent aqueous sodium hydroxide solution (50 ml) and heated at reflux for 2 hours. After cooling to room temperature, the mixture was acidified to pH 4 by addition of concentrated hydrochloric acid. The precipitate was filtered, washed with water (15 ml), rinsed with acetone (15 ml) and dried under vacuum to provide 3,8-dimethylxanthine (1.8 g).
With hydrogenchloride; In sodium hydroxide; acetic anhydride; A solution of <strong>[6972-82-3]5,6-diamino-1-methyluracil</strong> (2.5 g) in acetic anhydride (25 ml) was heated at reflux for 2 hours and then the acetic anhydride was evaporated under reduced pressure. The residue was dissolved in 10percent aqueous sodium hydroxide solution (50 ml) and heated at reflux for 2 hours. After cooling to room temperature, the mixture was acidified to pH 4 by addition of concentrated hydrochloric acid. The precipitate was filtered, washed with water (15 ml), rinsed with acetone (15 ml) and dried under vacuum to provide 3,8-dimethylxanthine (1.8 g).

 

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