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Chemical Structure| 1100598-49-9 Chemical Structure| 1100598-49-9

Structure of 1100598-49-9

Chemical Structure| 1100598-49-9

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Product Details of [ 1100598-49-9 ]

CAS No. :1100598-49-9
Formula : C8H8N4O
M.W : 176.18
SMILES Code : O=C1C=CC(C2=CN(C)N=C2)=NN1
MDL No. :MFCD16109164

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Application In Synthesis of [ 1100598-49-9 ]

* 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 [ 1100598-49-9 ]

[ 1100598-49-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 943541-20-6 ]
  • [ 1100598-49-9 ]
YieldReaction ConditionsOperation in experiment
98% With water; acetic acid; at 120℃; for 4h; A mixture of <strong>[943541-20-6]3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine</strong> (494 mg, 2.5 mmol) in AcOH (20 mL) was stirred at 120 C for 4 h. The reaction mixture was concentrated under reduced pressure, and water was added to the concentrates. The generated solids was filtered and dried to afford 6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3(2H)-one (431 mg, 98 %). 6-(1-Methyl-1H-pyrazol-4-yl)pyridazin-3(2H)-one (2a) 1HNMR (300 MHz, CDCl3) delta 8.70 (d, J = 11.3 Hz, 1H), 7.96(s, 1H), 6.94 (s, 1H), 6.62 (d, J = 11.3 Hz, 1H), 3.95 (s, 3H).
A suspension of 615 g (2.90 mol) of <strong>[943541-20-6]3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-pyridazine</strong> in a mixture of 1.86 l of formic acid and 2.61 l of water is heated to 80 C. with stirring and stirred at this temperature for 28 hours. The reaction mixture is cooled to room temperature, a little activated carbon is added, and the solid is filtered off with suction. The filtrate is adjusted to a pH of 7 using 40% aqueous sodium hydroxide solution with ice cooling and left at 6 C. for 16 h. The resultant precipitate is filtered off with suction, washed with water and dried in vacuo: 6-(1-methyl-1H-pyrazol-4-yl)-2H-pyridazin-3-one as colourless crystals; ESI 177.
  • 2
  • [ 298-12-4 ]
  • [ 37687-18-6 ]
  • [ 1100598-49-9 ]
YieldReaction ConditionsOperation in experiment
25% A stirred mixture of glyoxylic acid (21.46 g, 290 mmol) and 8 (9 g, 72.5 mmol) was heated at 120 C for 7 h. The reaction mixture was allowed to cool to 40 C and then H2O (200 mL) and conc. aq NH3·H2O (40 mL) was added sequentially. The mixture was extracted with EtOAc (150 mL * 4). The aqueous solution was stirred with 85% hydrazine hydrate (11 mL, 290 mmol) and heated under reflux for overnight. The resultant solid was collected by filtration and washed with H2O to give a yellow solid in 25% yield. 1H NMR (300 MHz, CD3OD) delta 8.07 (s, 1H), 7.89 (s, 1H), 7.79 (d, J = 9.8 Hz, 1H), 6.99 (d, J = 9.8 Hz, 1H), 3.93 (s, 3H).
 

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