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Chemical Structure| 211247-60-8 Chemical Structure| 211247-60-8

Structure of 211247-60-8

Chemical Structure| 211247-60-8

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Product Details of [ 211247-60-8 ]

CAS No. :211247-60-8
Formula : C13H19N3O2
M.W : 249.31
SMILES Code : O=[N+](C1=CC=C(N2CCC(N(C)C)CC2)C=C1)[O-]
MDL No. :MFCD11039486

Safety of [ 211247-60-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 211247-60-8 ]

* 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 [ 211247-60-8 ]

[ 211247-60-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4876-59-9 ]
  • [ 350-46-9 ]
  • [ 211247-60-8 ]
YieldReaction ConditionsOperation in experiment
90% With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 100℃; To a stirred solution of 135 1-fluoro-4-nitrobenzene (1 g, 7.08 mmol, 1.0 eq) in 95 DMSO (10 mL); 758 N,N-dimethylpiperidin-4-amine (1.56 g, 7.7 mmol, 2.5 eq) and 27 DIPEA (4.93 mL, 28.3 mmol) were added under stirring and resulting mixture was heated at 100 C. The progress of the reaction was monitored by LCMS. After completion reaction was cooled and quenched with ice cold water. The resulting solid precipitate was filtered, dried to afford 759 N,N-dimethyl-1-(4-nitrophenyl)piperidin-4-amine (1.6 g, 90%) as yellow solid. (0752) LCMS: 250 [M+1]+
77% With N-ethyl-N,N-diisopropylamine; at 95℃; for 18h;Inert atmosphere; Step 1: A mixture of l-fluoro-4-nitrobenzene (3.00 g, 21.3 mmol), N,N-dimethylpiperidin-4- amine dihydrochloride (4.70 g, 23.4 mmol) and DIPEA (15 mL, 86.1 mmol) was stirred at 95 C for 18 h. The mixture was cooled to room temperature, diluted with 1 : 1 EtOAc/hexanes (100 mL), washed twice with aq. calcium gluconate (100 mL each, 50% saturation), and the organic layer was separated and dried over anhydrous Na2S04 and concentrated to yield the desired product as a red oil (4.1 g, 77% yield). 1H NMR (DMSO-d6, 400 MHz) delta 8.03 (d, J = 9.6 Hz, 1H), 7.01 (d, J = 9.6 Hz, 1H), 4.04-4.01 (m, 2H), 3.02-2.95 (m, 2H), 2.39-2.32 (m, 1H), 2.17 (s, 6H), 1.85-1.81 (m, 2H), 1.44-1.34 (m, 2H); MS (ESI): calcd for C13H19N302: 249, found: 250 (MH+).
50% With triethylamine; In methanol; at 90℃; for 3.5h; Dimethyl-piperidin-4-yl-amine dihydrochloride (Aldrich, 2.0 g, 9.95 mmol) and 4-fluoro-nitrobenzene (Aldrich, 2.5 g, 17.7 mmol) were added to methanol (30 mL). The mixture was heated to 90 C. and stirred for 3.5 hours. The mixture was treated with 1 N HCl to pH=1 and then extracted with diethyl ether (2*10 mL). The aqueous layer was treated with saturated sodium carbonate to pH=10 and then extracted with methylene chloride (2*20 mL). The organic layer was dried with sodium sulfate and the solvent was removed to give the desired product. 1.25 g, 50%. MS (m+H)+: 250.
 

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