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Chemical Structure| 4876-56-6 Chemical Structure| 4876-56-6

Structure of 4876-56-6

Chemical Structure| 4876-56-6

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Product Details of [ 4876-56-6 ]

CAS No. :4876-56-6
Formula : C14H24Cl2N2
M.W : 291.26
SMILES Code : CN(C1CCN(CC2=CC=CC=C2)CC1)C.[H]Cl.[H]Cl

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Application In Synthesis of [ 4876-56-6 ]

* 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 [ 4876-56-6 ]

[ 4876-56-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4876-56-6 ]
  • [ 4876-59-9 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;palladium 10% on activated carbon; In water; isopropyl alcohol; at 20℃; for 22h; After adding 10% palladium-carbon (2.0 g) to a solution of the crude 4-dimethylamino-1-benzylpiperidine dihydrochloride (30.0 g) in 2-propanol (300 ml)-water (300 ml), the mixture was stirred for 22 hours at room temperature under a hydrogen atmosphere. The catalyst was filtered and washed with 2-propanol. The filtrate was then concentrated. The obtained crystals were suspended in ethanol (50 ml). They were then diluted with diethyl ether (50 ml). The crystals were subsequently filtered and washed with methanol (10 ml). They were then subjected to aeration drying to provide the title compound (16.4 g) as colorless crystals. 1H-NMR Spectrum (CD3OD) delta (ppm): 1.94-2.05 (2H, m), 2.35 (2H, m), 2.89 (6H, s), 3.06-3.16 (2H, m), 3.52-3.62 (3H, m).
With hydrogen;palladium 10% on activated carbon; In methanol; for 48h; To l-benzyl-N,N-dimethylpiperidin-4-amine dihydrochloride (6.7 g, 23 mmol) was added Pd/C (10%, 2.4 g) under argon. Methanol (100 ml) was added via syringe, and H2 gas was introduced and the mixture stirred vigorously under an atmosphere of H2. After 48 h, the mixture was flushed with nitrogen, filtered through celite and concentrated to afford a mixture of starting material and N,N-dimethylpiperidin-4-amine dihydrochloride as a white solid. This solid was treated with l-Fluoro-2-nitro-4- trifluoromethyl-benzene (3.2 ml, 22.9 mmol), triethylamine (12.7 ml, 92 mmol), and 50 ml dry THF. The mixture was heated to 75 0C with a water-cooled reflux condenser for 12 h. The mixture was allowed to cool to ambient temperature, was filtered through a fritted funnel, and concentrated to an orange oil. The residue was purified by silica gel chromatography (MC/MeOH/cone. NH4OH) to give the desired product as an orange oil. MS (m/z) : 318.1 (M+H)+. Calc'd for C14H18F3N3O2: 317.31.
 

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