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Chemical Structure| 116705-41-0 Chemical Structure| 116705-41-0

Structure of 116705-41-0

Chemical Structure| 116705-41-0

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Product Details of [ 116705-41-0 ]

CAS No. :116705-41-0
Formula : C8H10N4O4
M.W : 226.19
SMILES Code : O=C1NC(C([N+]([O-])=O)=C(/C=C/N(C)C)N1)=O
MDL No. :MFCD21607947

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Application In Synthesis of [ 116705-41-0 ]

* 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 [ 116705-41-0 ]

[ 116705-41-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 116705-41-0 ]
  • [ 65996-50-1 ]
YieldReaction ConditionsOperation in experiment
89.8% With acetic acid; zinc; 5.1.1.1 Pyrrolo[3,2-d]pyrimidin-2,4-dione (5) To a stirred slurry of (E)-6-(2-(dimethylamino)vinyl)-5-nitropyrimidin-2,4-dione 4<ce-sup primary_key="ce-sup-296167-none">35,38 (1 g, 4.4 mol) in fresh glacial AcOH (50 mL), Zinc dust (stabilized) (2 g) was added in two lots of 1 g with an interval of 1 h. Upon overnight stirring the yellow slurry changed to a pale yellow to off-white slurry which was filtered and the filtrate concentrated in vacuo to obtain brown syrup. The product was precipitated from the brown syrup using ethanol to obtain 4 as white solid (0.6 g, 89.8%). The spectral data agrees with reported data. 38 1H NMR (400 MHz, DMSO-d6): δ 5.82-5.83 (t, 1H, J = 2.28 Hz), 7.12-7.13 (t, 1H, J = 2.72 Hz, J = 2.96 Hz), 10.57 (s, 1H), 10.74 (s, 1H), 11.82 (s, 1H). 13C NMR (400 MHz, DMSO-d6): δ 96.5, 110.9, 127.4, 135.1, 152.0, 156.3.
89.8% With acetic acid; zinc; for 1h; To a stirred slurry of (E)-6-(2-(dimethylamino)vinyl)-5-nitropyrimidin-2,4-dione35,36 (1 g, 4.4 mol) in fresh glacial AcOH (50 mL), Zinc dust (stabilized) (2 g) was added in two lots of 1 g with an interval of 1 h. Upon overnight stirring the yellow slurry changed to a pale yellow to off-white slurry which was filtered and the filtrate concentrated in vacuo to obtain brown syrup. The product was precipitated from the brown syrup using ethanol to obtain as white solid (0.6 g, 89.8%). The spectral data agrees with reported data. 1H NMR (400 MHz, DMSO-d6): δ 5.82-5.83 (t, 1H, J=2.28 Hz), 7.12-7.13 (t, 1H, J=2.72 Hz, J=2.96 Hz), 10.57 (s, 1H), 10.74 (s, 1H), 11.82 (s, 1H). 13C NMR (400 MHz, DMSO-d6): δ 96.5, 110.9, 127.4, 135.1, 152.0, 156.3.
65% With acetic acid; zinc; at 80℃; for 2h; A suspension of 6-[(e)-2-(dimethylamino)vinyl]-5-nitropyrimidine- 2,4(1 H,3H)-dione (1.43g, 6.36 mmol) in acetic acid (23 mL) was heated to 80 then zinc dust (2 g, 30.77 mmol) was added slowly over 1 h. The resulting suspension was heated for a further 1 h then allowed to cool to room temperature. The solid was collected by filtration then washed with acetic acid. The solid was transferred to a beaker and washed with water (25 mL), collected then dissolved in sodium hydroxide (5%, 10 mL). This solution was warmed to 70 and stirred for 30 min. Acetic acid was added until pH 5-6 then the precipitate collected and washed with cold water then ethanol. The resultant solid was dried in vacuo to furnish lH-pyrrolo[3,2-d]pyrimidine- 2,4(3H,5H)-dione (0.62 g, 65%).
 

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