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Chemical Structure| 1279105-79-1 Chemical Structure| 1279105-79-1

Structure of 1279105-79-1

Chemical Structure| 1279105-79-1

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Product Details of [ 1279105-79-1 ]

CAS No. :1279105-79-1
Formula : C10H11N3O
M.W : 189.21
SMILES Code : OC1=CC(C2=CC=CN=C2)=NN1CC
MDL No. :MFCD28365964

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Application In Synthesis of [ 1279105-79-1 ]

* 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 [ 1279105-79-1 ]

[ 1279105-79-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6283-81-4 ]
  • [ 6629-60-3 ]
  • [ 1279105-79-1 ]
YieldReaction ConditionsOperation in experiment
22.5% With acetic acid; for 16h;Reflux; 2-Ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol: To <strong>[6283-81-4]3-oxo-3-pyridin-3-yl-propionic acid ethyl ester</strong> (500 mg, 3.57 mmol) in AcOH was added ethylhydrazine oxalate (231.9 mg, 3.86 mmol) and the mixture refluxed for 16 h. After which, the AcOH was evaporated and crude mass neutralized with aq. Na2CO3 solution. Following extraction with EtOAc, the organic phase was washed with brine, dried over Na2SO4 and concentrated. The crude material was purified by column chromatography using 2% MeOH-DCM as an eluent to give 2-ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol (110 mg, 22.5%) as a yellow solid.
22.5% With acetic acid; for 16h;Reflux; 2-Ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol: To <strong>[6283-81-4]3-oxo-3-pyridin-3-yl-propionic acid ethyl ester</strong> (500 mg, 3.57 mmol) in AcOH was added ethylhydrazine oxalate (231.9 mg, 3.86 mmol) and the mixture refluxed for 16 h. After which, the AcOH was evaporated and crude mass neutralized with aq. Na2CO3 solution. Following extraction with EtOAc, the organic phase was washed with brine, dried over Na2SO4 and concentrated. The crude material was purified by column chromatography using 2% MeOH-DCM as an eluent to give 2-ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol (110 mg, 22.5%) as a yellow solid.
22.5% With acetic acid; for 16h;Reflux; To <strong>[6283-81-4]3-oxo-3-pyridin-3-yl-propionic acid ethyl ester</strong> (500 mg, 3.57 mmol) in AcOH was added ethylhydrazine oxalate (231.9 mg, 3.86 mmol) and the mixture refluxed for 16 h. After which, the AcOH was evaporated and crude mass neutralized with aq. Na2CO3 solution. Following extraction with EtOAc, the organic phase was washed with brine, dried over Na2SO4 and concentrated. The crude material was purified by column chromatography using 2% MeOH-DCM as an eluent to give 2-ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol (110 mg, 22.5%) as a yellow solid.
22.5% With acetic acid; for 16h;Reflux; To <strong>[6283-81-4]3-oxo-3-pyridin-3-yl-propionic acid ethyl ester</strong> (500 mg, 3.57 mmol) in AcOH was added ethylhydrazine oxalate (231.9 mg, 3.86 mmol) and the mixture refluxed for 16 h. After which, the AcOH was evaporated and crude mass neutralized with aq. Na2CO3 solution. Following extraction with EtOAc, the organic phase was washed with brine, dried over Na2SO4 and concentrated. The crude material was purified by column chromatography using 2% MeOH-DCM as an eluent to give 2-ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol (110 mg, 22.5%) as a yellow solid.
22.5% In acetic acid; for 16h;Reflux; To <strong>[6283-81-4]3-oxo-3-pyridin-3-yl-propionic acid ethyl ester</strong> (500 mg, 3.57 mmol) in AcOH was added ethylhydrazine oxalate (231.9 mg, 3.86 mmol) and the mixture refluxed for 16 h. After which, the AcOH was evaporated and crude mass neutralized with aq. Na2CO3 solution. Following extraction with EtOAc, the organic phase was washed with brine, dried over Na2SO4 and concentrated. The crude material was purified by column chromatography using 2% MeOH-DCM as an eluent to give 2-ethyl-5-pyridin-3-yl-2H-pyrazol-3-ol (110 mg, 22.5%) as a yellow solid.

 

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