Alternatived Products of [ 21626-41-5 ]
Product Details of [ 21626-41-5 ]
CAS No. : | 21626-41-5 |
MDL No. : | MFCD00023436 |
Formula : |
C12H11N3O2
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Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | - |
M.W : | 229.24 g/mol |
Pubchem ID : | - |
Synonyms : |
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Safety of [ 21626-41-5 ]
Signal Word: | |
Class: | |
Precautionary Statements: | |
UN#: | |
Hazard Statements: | |
Packing Group: | |
Application In Synthesis of [ 21626-41-5 ]
* 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 [ 21626-41-5 ]
Yield | Reaction Conditions | Operation in experiment |
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(yield)98percent; |
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2-Chlor-5-nitro-pyridin, Benzylamin; |
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2-Chlor-5-nitropyridin, Benzylamin; |
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2-Chlor-5-nitro-pyridin, Benzylamin; |
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- 2
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[ 100-46-9 ]

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[ 21626-41-5 ]
Yield | Reaction Conditions | Operation in experiment |
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With ethanol |
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- 3
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potassium 5-nitropyridine-2-sulfonate
[ No CAS ]

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[ 100-46-9 ]

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[ 21626-41-5 ]
Yield | Reaction Conditions | Operation in experiment |
106 mg |
In water at 23℃; for 20h; |
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- 4
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[ 2530-26-9 ]

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[ 100-46-9 ]

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4,6-bis(benzylamino)-3-nitropyridine
[ No CAS ]

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2,6-bis(benzylamino)-3-nitropyridine
[ No CAS ]

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[ 21626-41-5 ]
Yield | Reaction Conditions | Operation in experiment |
64% |
With AgPy2MNo4 at 8 - 10℃; for 0.5h; |
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- 5
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[ 4548-45-2 ]

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[ 100-46-9 ]

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[ 21626-41-5 ]
Yield | Reaction Conditions | Operation in experiment |
87% |
With triethylamine In isopropyl alcohol for 3h; Reflux; Inert atmosphere; |
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With hydrogenchloride In ethanol |
1.1 1.
1. 2-Benzylamino-5-nitropyridine A solution of 2-chloro-5-nitropyridine (1.59 g, 10 mmol) and benzylamine (2.3 mL, 21 mmol) in ethanol (10 mL) was heated at reflux for 2 h. The reaction mixture was allowed to ambient temperature, 1.2 N HCl was added, the precipitate collected, rinsed with water, and dried to give 2.02 g of 2-benzylamino-5-nitropyridine as a yellow solid. |
Reference:
[1]Kinarivala, Nihar; Patel, Ronak; Boustany, Rose-Mary; Al-Ahmad, Abraham; Trippier, Paul C.
[Journal of Medicinal Chemistry, 2017, vol. 60, # 23, p. 9739 - 9756]
[2]Current Patent Assignee: LIGAND PHARMACEUTICALS INC - US6143760, 2000, A
- 6
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[ 21626-41-5 ]

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[ 21630-48-8 ]
Yield | Reaction Conditions | Operation in experiment |
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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. |
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With hydrazine hydrate In 1,4-dioxane at 20℃; Inert atmosphere; |
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Reference:
[1]Current Patent Assignee: LIGAND PHARMACEUTICALS INC - US6143760, 2000, A
[2]Kinarivala, Nihar; Patel, Ronak; Boustany, Rose-Mary; Al-Ahmad, Abraham; Trippier, Paul C.
[Journal of Medicinal Chemistry, 2017, vol. 60, # 23, p. 9739 - 9756]
- 7
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[ 4214-76-0 ]

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[ 100-51-6 ]

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[ 21626-41-5 ]
Yield | Reaction Conditions | Operation in experiment |
27% |
With water; palladium diacetate; sodium 3-(diphenylphosphanyl)benzenesulfonate In n-heptane at 120℃; for 17h; Sealed tube; |
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