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Chemical Structure| 1022091-74-2 Chemical Structure| 1022091-74-2

Structure of 1022091-74-2

Chemical Structure| 1022091-74-2

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Product Details of [ 1022091-74-2 ]

CAS No. :1022091-74-2
Formula : C8H10N6
M.W : 190.21
SMILES Code : CN1N=CC(C2=NN=C(NN)C=C2)=C1
MDL No. :MFCD16169018

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Application In Synthesis of [ 1022091-74-2 ]

* 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 [ 1022091-74-2 ]

[ 1022091-74-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 943541-20-6 ]
  • [ 1022091-74-2 ]
YieldReaction ConditionsOperation in experiment
90.4% With hydrazine hydrate; In ethanol; at 4℃; for 18h;Reflux; Preparation 2 3-Hydrazinyl-6-(1-methyl-1H-pyrazol-4-yl)pyridazine To a 1000 mL round bottom flask containing a solution of hydrazine monohydrate (280 mL, 4.89 mol) in ethanol (300 mL) is added <strong>[943541-20-6]3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine</strong> (60 g, 308.3 mmol) at 4 C. The resulting clear solution is heated to reflux for 18 h, and then cooled to 10 C. The product precipitated is collected by filtration and dried under vacuum to give the title compound as a white solid (53 g, 90.4%) and is used as is.
90% With hydrazine hydrate; In ethanol; for 18h;Cooling with ice; Reflux; To 100 ml of ethanol is added to the flask (40 ml) as the solvent, then steps are sequentially added under ice bath 1 (HJ-8) made of (1.90g) and hydrazine hydrate (3.5 ml), stirring 10 minutes evacuation goes to the ice-bath, heated up to reflow. Reaction 18 hours later, cold to 10 C, a white solid precipitated. Buchner filter for filtering, the filter cake is washed with cold ethanol washing 2 times, vacuum drying, to obtain 3-hydrazino-6 - (1-methyl -1H-pyrazol-4-yl) pyridazine (HJ-9) 1.68g, yield 90%
87% With hydrazine; In ethanol; for 18h;Heating / reflux; Step 2: [6-(l-Methyl-ljfiT-pyrazol-4-yl)-pyridazin-3-yl]-hydrazine; [0346] To a suspension of 3-chloro-6-(l-methyl-lH-pyrazole-4-yl)-pyridazine (21.0 g, 108 mmol) in ethanol (370 mL) was added hydrazine monohydrate (36 mL). The reaction mixture was stirred at reflux for 18h, then cooled to room temperature. The precipitate was collected via filtration, washed with cold ethanol and dried in vacuo to provide 18 g of [6- (1 -methyl- lH-pyrazol-4-yl)-pyridazin-3-yl]-hydrazine as a beige solid (87% yield): 1HNMR (DMSO-ct°) delta 3.88 (s, 3H), 4.28 (s, 2H), 7.02 (d, IH), 7.59 (d, IH), 7.83 (s, IH), 7.91 (s, IH), 8.19 (s, IH); MS (m/z) 191 [M+H+]+.
 

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