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Chemical Structure| 939979-34-7 Chemical Structure| 939979-34-7

Structure of 939979-34-7

Chemical Structure| 939979-34-7

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Product Details of [ 939979-34-7 ]

CAS No. :939979-34-7
Formula : C8H11N3O3
M.W : 197.19
SMILES Code : O=C(C1=C(NC(N)=O)C=CN1)OCC

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Application In Synthesis of [ 939979-34-7 ]

* 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 [ 939979-34-7 ]

[ 939979-34-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 939979-34-7 ]
  • [ 65996-50-1 ]
YieldReaction ConditionsOperation in experiment
(3) To ethyl 3-ureido-1H-pyrrolo-2-carboxylate (69.4g) was added aqueous 6% sodium hydroxide solution (950ml) and the mixture was stirred under reflux for 30 minutes. After being cooled, the reaction solution was adjusted to pH6 with concentrated hydrochloric acid and after stirring, the crystals were filtered. The filtrate was washed with a small amount of water and methanol, concentrated in vacuo and subjected to azeotropic distillation with toluene to give 1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione (32.0g). APCI-MS (m/e): 152 (M+H)+
(3) A 6% aqueous sodium hydroxide solution (950 mL) was added to 3-ureido-1H-pyrrolo-2-carboxylic acid ethyl ester(69.4 g) and the mixture was refluxed under heating with stirring for 30 minutes. After standing to cool, the reaction mixture was adjusted to pH 6 by adding conc.hydrochloric acid and the precipitate was filtered after stirring. It was washed with a little amount of water and methanol, dried under reduced pressure and azeotropically distilled with toluene to give 1,5-dihydro-pyrrolo[3,2-d]pyrimidin-2,4-dione(32 g). APCI-MS(m/e):152[M+H]+.
With sodium hydroxide; In water; for 0.5h;Reflux; To a stirred solution of ethyl 3-ureido-1H-pyrrole-2-carboxylate (26.2 mmol) in H20 (95 mL) was added NaOH (6 g). After stirred at refluxing for 30 mm, the reaction mixture was cooled down to room temperature and acidified to pH 6 by conc. HC1, the brown solid was collected by filtration to provide 1,5- dihydro-2H-pyrrolo[3,2-djpyrimidine-2,4(3H)-dione (1.8 g, 45 % over 2 steps) which was used in the next step without purification. LC-MS (ESI): m/z (M+1) 152.02.
1.8 g With sodium hydroxide; In water; for 0.5h;Reflux; [00473] To a stirred solution of ethyl3-ureido-1H-pyrrole-2-carboxylate (26.2 mmol) in H20 (95 mL) wasadded NaOH (6 g). After stirred at refluxing for 30 min, the reaction mixture was cooled down to roomtemperature and acidified to pH~ 6 by cone. HCl, the brown solid was collected by filtration to provide 1,5-dihydro-2H-pyrrolo[3,2-d]pyrimidine-2,4(3H)-dione (1.8 g, 45% over 2 steps) which was used in the nextstep without purification. LC-MS (ESI): m/z (M+1) 152.02

 

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