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Chemical Structure| 1089279-90-2 Chemical Structure| 1089279-90-2

Structure of 1089279-90-2

Chemical Structure| 1089279-90-2

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Product Details of [ 1089279-90-2 ]

CAS No. :1089279-90-2
Formula : C14H21N3O3
M.W : 279.34
SMILES Code : CN(C)C1CCN(C2=CC=C([N+]([O-])=O)C(OC)=C2)CC1
MDL No. :MFCD22190905

Safety of [ 1089279-90-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1089279-90-2 ]

* 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 [ 1089279-90-2 ]

[ 1089279-90-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 448-19-1 ]
  • [ 4876-59-9 ]
  • [ 1089279-90-2 ]
YieldReaction ConditionsOperation in experiment
85.3% With potassium carbonate; In acetonitrile; at 85℃;Large scale; At room temperature, a 100-L reaction kettle was charged with Compound 1 (13.80 kg), Compound 2 (9.78 kg), and acetonitrile (70 L), and stirred to dissolve. Potassium carbonate (27.66 kg) was added, mechanically stirred, the temperature was raised to 85 C, and the reaction was allowed to proceed overnight. The mixture was filtered under reduced pressure to room temperature, and the filtrate was distilled under reduced pressure. The obtained solid was mechanically slurried with n-heptane (40L) and isopropyl ether (20L) overnight. The compound 3 was 16.22 kg as a yellow powdery solid with a filtration rate of 85.3%. .
75.9% With potassium carbonate; In acetonitrile; at 60℃; for 3h;Inert atmosphere; Add compound 1 to a 50 mL single-mouth flask equipped with magnetic stirring(887 mg, 4.72 mmol) and acetonitrile(20 mL), stirred and dissolved, added the dihydrochloride salt of compound 22 (1.1 g, 5.66 mmol)And potassium carbonate (2.2 g, 15.57 mmol),The reaction mixture was heated to 60 C under a nitrogen atmosphere and stirred for 3 hours while stirring.Cool to room temperature, distill off the solvent under reduced pressure and add water (60 mL).A large amount of yellow solid was precipitated, filtered, washed with water (10 mL) and dried to give a yellow solid1.0g,The yield was 75.9%.
 

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