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Chemical Structure| 6647-92-3 Chemical Structure| 6647-92-3

Structure of 6647-92-3

Chemical Structure| 6647-92-3

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Product Details of [ 6647-92-3 ]

CAS No. :6647-92-3
Formula : C5H7N3O
M.W : 125.13
SMILES Code : CC(NC1=CNN=C1)=O
MDL No. :MFCD12194780

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Application In Synthesis of [ 6647-92-3 ]

* 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 [ 6647-92-3 ]

[ 6647-92-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 28466-26-4 ]
  • [ 108-24-7 ]
  • [ 6647-92-3 ]
YieldReaction ConditionsOperation in experiment
54% at 0 - 20℃; Intermediate Example 17.N-( 1 H-pyrazol-4-yl)acetamide Acetic anhydride (0.7 ml, 8.433 mmol.) was added dropwise at 0 C to 1H- pyrazol-4-amine (0.7 g, 8.433 mmol). The mixture was stirred for 30 min at RT and quenched by the addition of crushed ice. The mixture was extracted with ethyl acetate The combined organic layer was washed with water, brine and dried over sodium sulphate. The solvent was distilled off to afford the product in 54 % yield. (0.6 g). LC- MS (ESI): Calculated mass: 125.0; Observed massl26.0 [M+H] + (rt: 0.115 min).
54% at 20℃; for 0.5h; Acetic anhydride (0.7 ml, 8.433 mmol) was added dropwise at 0 C. to <strong>[28466-26-4]1H-pyrazol-4-amine</strong> (0.7 g, 8.433 mmol). The mixture was stirred for 30 min at RT and quenched by the addition of crushed ice. The mixture was extracted with ethyl acetate The combined organic layer was washed with water, brine and dried over sodium sulphate. The solvent was distilled off to afford the product in 54% yield. (0.6 g). LC-MS (ESI): Calculated mass: 125.0; Observed mass 126.0 [M+H]+ (rt: 0.115 min).
 

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