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Chemical Structure| 123313-07-5 Chemical Structure| 123313-07-5

Structure of 123313-07-5

Chemical Structure| 123313-07-5

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Product Details of [ 123313-07-5 ]

CAS No. :123313-07-5
Formula : C4H8N4O
M.W : 128.13
SMILES Code : O=C1NN=C(C)CN1N

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Application In Synthesis of [ 123313-07-5 ]

* 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 [ 123313-07-5 ]

[ 123313-07-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 22346-73-2 ]
  • [ 123313-07-5 ]
  • [ 133299-01-1 ]
YieldReaction ConditionsOperation in experiment
In ethanol; Example H4 2,3,4,5-tetrahydro-3-oxo-4[(pyridin-N-oxide-3-yl)-methyleneamino]-6-methyl-1,2,4-triazine To a solution of 2.56 g (0.02 mol) 2,3,4,5-tetrahydro-3-oxo-4-amino-6-methyl-1,2,4-triazine in 25 ml of ethanol are added 2.44 g (0.02 mol) of pyridine-3-carbaldehyde-N-oxide. The reaction mixture is refluxed for 1/2 hour, then cooled, and the precipitated solid is isolated by filtration, washed with ether and dried. The title compound of formula STR27 is obtained in the form of a white solid; m.p. 242-244 C. (yield: 3.6 g; 84%).
  • 2
  • [ 173282-69-4 ]
  • [ 123313-07-5 ]
  • (E)-6-methyl-4-((6-phenoxypyridin-3-yl)methyleneamino)-4,5-dihydro-1,2,4-triazin-3(2H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
65% With toluene-4-sulfonic acid; In methanol; for 6h;Reflux; To a solution of 1 (0.51 g, 4.00 mmol) and <strong>[173282-69-4]6-phenoxynicotinaldehyde</strong> (4) (0.80 g, 4.00 mmol) in methanol (50 mL) was added p-toluene sulfonic acid (0.14 g, 0.80 mmol), and then the mixture was refluxed for 6 h. The solution was cooled and then concentrated under reduced pressure. The crude product was purified by recrystallization using methanol to give compound II as a white solid (0.80 g, 65%); mp = 200-201 C; 1H NMR (400 MHz, DMSO-d6): δ 10.10 (s, 1H, NH), 8.37 (s, 1H, N=CH), 8.20 (d, J = 8.8 Hz, 1H, Py-H), 7.89 (s, 1H, Py-H), 7.44 (t, J = 7.6 Hz, 2H, Ar-H), 7.24 (t, J = 7.6 Hz, 1H, Ar-H), 7.17 (d, J = 7.6 Hz, 2H, Ar-H), 7.11 (d, J = 8.8 Hz, 1H, Py-H), 4.35 (s, 2H, CH2), 1.94 (s, 3H, CH3); 13C NMR (100 MHz, DMSO-d6) δ 163.6, 153.6, 147.3, 146.9, 144.0, 137.8, 136.8, 129.8, 126.7, 124.9, 121.4, 111.9, 47.7, 20.2. ESI-HRMS (m/z): Calcd for C16H16N5O2 [M+H]+ 310.1299. Found 310.1300.
65% With toluene-4-sulfonic acid; for 6h;Reflux; In a 250 mL single-mouth bottle, add aminotriazinone (I) (0.5I g, 4 mmol),P-toluenesulfonic acid (0.I4 g, 0.8 mmol) and methanol (I20 mL) were stirred and dissolved.Then 6-phenoxypyridine-3-carbaldehyde (3) (0.80 g, 4 mmol) was added and heated to reflux for 6 h.The reaction was monitored by TLC. After the reaction solution is decomposed under reduced pressure,Recrystallization from methanol gave 0.80 g of a white solid.Yield 65%.
 

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