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Chemical Structure| 353258-16-9 Chemical Structure| 353258-16-9

Structure of 353258-16-9

Chemical Structure| 353258-16-9

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Product Details of [ 353258-16-9 ]

CAS No. :353258-16-9
Formula : C10H13N3O3
M.W : 223.23
SMILES Code : OC1CCN(CC1)C1=NC=C(C=C1)[N+]([O-])=O
MDL No. :MFCD01310144

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Application In Synthesis of [ 353258-16-9 ]

* 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 [ 353258-16-9 ]

[ 353258-16-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 353258-16-9 ]
  • [ 476342-37-7 ]
YieldReaction ConditionsOperation in experiment
89% With hydrogen;palladium 10% on activated carbon; In ethanol; at 20℃; for 3.0h; Example 18C. l-(5-Aminopyridin-2-yl)piperidin-4-ol [00153] A solution of l-(5-nitropyridin-2-yl)piperidin-4-ol (Example, 18B, 0.6g, 2.6 mmol) in ethanol was added 10% palladium on carbon (0.3 g) and the mass was stirred at RT with hydrogen bladder for 3 h. Reaction mass was filtered through CELITE and concentrated to remove ethanol to yield Example 18C (0.45 g, 89% yield) as a brown oil. LC-MS, [M+H]+ = 194. 1U NMR (CD3OD, 400MHz): delta 7.70 (d, J = 2.6 Hz, IH), 7.10 (dd, J = 2.6, 8.8 Hz, IH), 6.73 (d, J = 8.8 Hz, IH), 3.76 (m, 3H), 2.91 (m, 2H), 1.89 (m, 2H), 1.51 (m, 2H).
51% With hydrogenchloride; iron; In ethanol; water; at 90℃; for 2.0h; To a suspension of 1.35g (6.04mmol) of the compound obtained in the Manufacturing Example 73 in 18mL of ethanol and 3mL of water were added 1.3g of reduced iron and 0.25mL of conc. hydrochloric acid, and the mixture was stirred for 2 hours at 90C. After cooling the reaction mixture, the mixture was filtrated by Celite and filtrate was condensed under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: dichloromethane/methanol = 10/1) to give 601mg (51%) of the title compound.
  • 2
  • [ 4548-45-2 ]
  • [ 5382-17-2 ]
  • [ 353258-16-9 ]
 

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