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[ CAS No. 21630-48-8 ] {[proInfo.proName]}

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Chemical Structure| 21630-48-8
Chemical Structure| 21630-48-8
Structure of 21630-48-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 21630-48-8 ]

CAS No. :21630-48-8 MDL No. :MFCD00023436
Formula : C12H11N3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 229.24 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 21630-48-8 ]

* 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 [ 21630-48-8 ]

[ 21630-48-8 ] Synthesis Path-Downstream   1~10

YieldReaction ConditionsOperation in experiment
2-Benzylamino-5-nitropyridin, Ra/Ni, H2;
  • 2
  • [ 21626-41-5 ]
  • [ 21630-48-8 ]
YieldReaction ConditionsOperation in experiment
In ethanol; dichloromethane 1.2 2. 2. 2-Benzylamino-5-aminopyridine A mixture of 2-benzylamino-5-nitropyridine (2.02 g) and 10% Pd/C (202 mg) in ethanol (20 mL) was placed in a Paar bottle and shaken under hydrogen (50 PSI) for 3 h. The mixture was filtered through Celite using dichloromethane and concentrated in vacuo to afford 1.76 g of 2-benzylamino-5-aminopyridine as a burgundy oil.
With hydrazine hydrate In 1,4-dioxane at 20℃; Inert atmosphere;
  • 3
  • [ 21630-48-8 ]
  • [ 87-13-8 ]
  • diethyl (2-benzylamino-5-pyridylaminomethylene)malonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
1.3 3. 3. Diethyl(2-benzylamino-5-pyridylaminomethylene)malonate A mixture of 2-benzylamino-5-aminopyridine (1.76 g) and diethyl ethoxymethylenemalonate (1.78 mL, 8.82 mmol) was heated at 130° C. for 2 h. While warm, the mixture was evacuated. After cooling, the product was triturated with 2:1 hexanes/ether and collected to give 2.74 g of diethyl (2-benzylamino-5-pyridylaminomethylene)malonate as a gold solid.
  • 4
  • 1-{N-[5-(benzo[1,3]dioxol-5-ylazo)pyridin-2-yl]-N-benzylamino}pyridinium bromide [ No CAS ]
  • [ 21630-48-8 ]
  • [ 14268-66-7 ]
YieldReaction ConditionsOperation in experiment
With formic acid; platinum on carbon; triethylamine In acetonitrile at 0℃; regioselective reaction;
  • 5
  • [ 46224-49-1 ]
  • [ 21630-48-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: potassium carbonate / dichloromethane / 0.33 h / Cooling with ice 2: acetone / 72 h / 20 °C / Inert atmosphere 3: triethylamine; platinum on carbon; formic acid / acetonitrile / 0 °C
  • 6
  • pyridinium N-[5′-(benzo[1,3]dioxol-5-ylazo)pyridin-2-yl]aminide [ No CAS ]
  • [ 21630-48-8 ]
  • [ 14268-66-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: acetone / 72 h / 20 °C / Inert atmosphere 2: triethylamine; platinum on carbon; formic acid / acetonitrile / 0 °C
  • 7
  • [ 100-39-0 ]
  • [ 21630-48-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: acetone / 72 h / 20 °C / Inert atmosphere 2: triethylamine; platinum on carbon; formic acid / acetonitrile / 0 °C
  • 8
  • [ 541-41-3 ]
  • [ 21630-48-8 ]
  • ethyl (6-(benzylamino)pyridin-3-yl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
26% In 1,4-dioxane at 20℃; Inert atmosphere; Darkness;
  • 9
  • [ 4548-45-2 ]
  • [ 21630-48-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: triethylamine / isopropyl alcohol / 3 h / Reflux; Inert atmosphere 2: hydrazine hydrate / 1,4-dioxane / 20 °C / Inert atmosphere
  • 10
  • [ 100-46-9 ]
  • [ 21630-48-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: triethylamine / isopropyl alcohol / 3 h / Reflux; Inert atmosphere 2: hydrazine hydrate / 1,4-dioxane / 20 °C / Inert atmosphere
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