Alternatived Products of [ 516455-57-5 ]
Product Details of [ 516455-57-5 ]
CAS No. : | 516455-57-5 |
MDL No. : | MFCD03759867 |
Formula : |
C11H10N4O
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | RRXNULSELUJDDO-UHFFFAOYSA-N |
M.W : |
214.22
|
Pubchem ID : | 719005 |
Synonyms : |
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Safety of [ 516455-57-5 ]
Application In Synthesis of [ 516455-57-5 ]
* 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 [ 516455-57-5 ]
- 1
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[ 15108-18-6 ]
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[ 141-97-9 ]
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[ 516455-57-5 ]
Yield | Reaction Conditions | Operation in experiment |
|
In acetic acid; at 20℃; for 2h; |
General procedure: A mixture of 2-hydrazino-5-methyl-benzimidazole (3, 1.0g, 6.17mmol) and ethyl 2-acetyl-3-phenylpropanoate (4, 1.4mL, 6.59mmol) in acetic acid (20mL) was stirred for 2h at ambient temperatures. To a mixture of acetonitrile (100mL) and water (100mL) was added the reaction mixture. After stirring at ambient temperatures, the resulting precipitates were collected by filtration and washed with acetonitrile in water (1:1). The precipitates was purified by recrystallization from ethanol (95mL) to generate 3-methyl-1-(5-methyl-1H-benzimidazol-2-yl)-4-benzyl-1H-pyrazol-5-ol (35, 0.64g, 32.6%). The other compounds studied in this work (5-52) were prepared in a similar manner. The typical experimental procedure for synthesizing and evaluating the compounds used in this study, in addition to the analytical data and the estimated purity (HPLC) of the biologically relevant compounds, are provided in Supplemental data and Table S1, respectively. |