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N2-(1-Benzylpiperidin-4-yl)pyridine-2,3-diaMine synthesis

2synthesis methods
185058-54-2 Synthesis
N-(1-Benzylpiperidin-4-yl)-3-nitropyridin-2-amine

185058-54-2
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N2-(1-Benzylpiperidin-4-yl)pyridine-2,3-diaMine

185058-55-3
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Yield:-

Reaction Conditions:

with hydrogenchloride;stannous chloride in tetrahydrofuran;ethyl acetate;

Steps:

99.B Step B

Step B 2-N-(1-Benzyl-piperidin-4-yl)-pyridine-2,3-diamine To a solution of (1-Benzyl-piperidin-4-yl)-(3-nitro-pyridin-2-yl)-amine (from Step A) in 10 mL of THF was added 2.4 g of SnCl2 and 1 mL of concentrated HCl at room temperature, stirred at room temperature for 2 hours. The reaction was diluted with 40 mL of EtOAc and washed with 30 mL of saturated NaHCO3 aqueous solution. After separating layers, the aqueous phase was extracted with 2*15 mL EtOAc. The combined organic phases were washed with 15 mL of brine, dried over MgSO4 and concentrated under reduced pressure to give 603 mg of yellow soid.

References:

US6248755,2001,B1