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Chemical Structure| 15579-82-5 Chemical Structure| 15579-82-5

Structure of 15579-82-5

Chemical Structure| 15579-82-5

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Product Details of [ 15579-82-5 ]

CAS No. :15579-82-5
Formula : C5H7N3O
M.W : 125.13
SMILES Code : NC1=CN=CN=C1OC
MDL No. :MFCD09746186

Safety of [ 15579-82-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 15579-82-5 ]

* 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 [ 15579-82-5 ]

[ 15579-82-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52854-14-5 ]
  • [ 15579-82-5 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogen;palladium 10% on activated carbon; In ethanol; at 20℃; under 1500.15 Torr; b) 4-Methoxypyrimidin-5-amine 10% Palladium on carbon (1.10 g) was added to a solution of <strong>[52854-14-5]4-chloro-6-methoxy-5-nitropyrimidine</strong> (Preparation 25a, 1.97 g, 10.4 mmol) in ethanol (80 mL) and the reaction mixture was stirred at ambient temperature overnight under a hydrogen atmosphere at a pressure of 2 bars. The mixture was then filtered through Celite and the filter cake was washed with ethanol. The combined filtrate and washings were concentrated to give the title compound (1.30 g, 100%) as a solid. LRMS (m/z): 126 (M+1)+. 1H NMR delta (300 MHz, DMSO-d6): 4.11 (s, 3H), 7.91 (s, 1 H), 8.59 (s, 1 H).
100% With hydrogen;10% Pt/activated carbon; In ethanol; at 20℃; under 1500.15 Torr; b) 4-Methoxypyrimidin-5-amine10% Palladium on carbon (1 .10 g) was added to a solution of 4-chloro-6-methoxy-5- nitropyrimidine (Preparation 76a, 1 .97 g, 10.4 mmol) in ethanol (80 mL) and the reaction mixture was stirred at ambient temperature overnight under a hydrogen atmosphere at a pressure of 2 bars. The mixture was then filtered through Celite and the filter cake was washed with ethanol. The combined filtrate and washings were concentrated to give the title compound (1 .30 g, 100%) as a solid.LRMS (m/z): 126 (M+1 )+.1H NMR delta (300 MHz, DMSO-d6): 4.1 1 (s, 3H), 7.91 (s, 1 H), 8.59 (s, 1 H).
With hydrogen;5%-palladium/activated carbon; In ethanol; at 20℃; under 1500.15 Torr; for 16.0h; 4-Chloro-6-methoxy-5-nitropyrimidine (0.6g) and 5% Pd on carbon (0.6g) in ethanol(90mL) and under hydrogen (2 bar) was stirred at room temperature for 16h. The mixturewas filtered through a pad of celite and evaporated under reduced pressure to give thesubtitle compound (0.35g).
 

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