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Chemical Structure| 4945-46-4 Chemical Structure| 4945-46-4

Structure of 4945-46-4

Chemical Structure| 4945-46-4

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6-(Piperidin-1-yl)pyridin-2-amine

CAS No.: 4945-46-4

,98%

4.5 *For Research Use Only !

Cat. No.: A1412706 Purity: 98%

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    Product Details of [ 4945-46-4 ]

    CAS No. :4945-46-4
    Formula : C10H15N3
    M.W : 177.25
    SMILES Code : NC1=NC(N2CCCCC2)=CC=C1
    MDL No. :MFCD19543781

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    Application In Synthesis of [ 4945-46-4 ]

    * 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 [ 4945-46-4 ]

    [ 4945-46-4 ] Synthesis Path-Downstream   1~1

    • 1
    • [ 110-89-4 ]
    • [ 1597-32-6 ]
    • [ 4945-46-4 ]
    YieldReaction ConditionsOperation in experiment
    94% at 205℃; for 0.5h;Microwave irradiation; A suspension of <strong>[1597-32-6]6-fluoropyridin-2-amine</strong> (500 mg, 4.4 mmol), piperidine (1.4 mL, 14.1 mmol) in water (0.5 mL) was heated to 205 C. in a microwave oven for 30 minutes. The reaction mixture was purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=3:1) to give 6-(piperidin-1-yl)pyridin-2-amine (740 mg, 94%) as a light yellow oil. LC-MS: [M+H]+, 178.1, tR=0.974 min.
    94% In water; at 205℃; for 0.5h;Microwave irradiation; A suspension of <strong>[1597-32-6]6-fluoropyridin-2-amine</strong> (500 mg, 4.4 mmol), piperidine (1.4 mL , 14.1 mmol) in water (0.5 mL) was heated to 205 C in a microwave oven for 30 minutes. The reaction mixture was purified by chromatography (silica gel, 200 - 300 mesh, petroleum ether : ethyl acetate = 3 : 1) to give 6-(piperidin-l-yl)pyridin-2-amine(740 mg, 94 %) as a light yellow oil. LC-MS : [M+H]+, 178.1 , tR = 0.974min.
     

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