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[ CAS No. 1416146-93-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1416146-93-4
Chemical Structure| 1416146-93-4
Structure of 1416146-93-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1416146-93-4 ]

CAS No. :1416146-93-4 MDL No. :N/A
Formula : C9H12ClN3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 229.66 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1416146-93-4 ]

* 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 [ 1416146-93-4 ]

[ 1416146-93-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1416146-93-4 ]
  • [ 1314978-36-3 ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid In dichloromethane at 20℃; for 0.5h; 15.B Step B.5-chloropyridazin-3-amine A mixture of tert-butyl N-(5-chloropyridazin-3-yl)carbamate (1.70 g, 7.40 mmol) and trifluoroacetic acid (15.4 g, 135 mmol, 10.0 mL) in dichloromethane (20 mL) was stirred for 0.5 hour at 20 °C. The reaction mixture was then concentrated under reduced pressure to provide the title compound: LCMS m/z 259.0 [M+H]+.
With trifluoroacetic acid In dichloromethane at 20℃; for 0.5h; 15.B Step B.5-chloropyridazin-3-amine A mixture of tert-butyl N-(5-chloropyridazin-3-yl)carbamate (1.70 g, 7.40 mmol) and trifluoroacetic acid (15.4 g, 135 mmol, 10.0 mL) in dichloromethane (20 mL) was stirred for 0.5 hour at 20 °C. The reaction mixture was then concentrated under reduced pressure to provide the title compound: LCMS m/z 259.0 [M+H]+.
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