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Chemical Structure| 1140507-92-1 Chemical Structure| 1140507-92-1

Structure of 1140507-92-1

Chemical Structure| 1140507-92-1

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Product Details of [ 1140507-92-1 ]

CAS No. :1140507-92-1
Formula : C14H15F3N2
M.W : 268.28
SMILES Code : N#CC1=CC=C(N2C(C)CCCC2)C(C(F)(F)F)=C1
MDL No. :MFCD27991760

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Application In Synthesis of [ 1140507-92-1 ]

* 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 [ 1140507-92-1 ]

[ 1140507-92-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67515-59-7 ]
  • [ 109-05-7 ]
  • [ 1140507-92-1 ]
YieldReaction ConditionsOperation in experiment
at 100℃; for 12h; A mixture of 4-fluro 3-trifluoro-methylbenzonitrile (ABCR F043738; 25 g; 132 mmol; 1 eq.) and 2-methylpiperidine (30.3 ml 264 mmol; 2 eq.) was stirred at 100 C 12 hours. The reaction mixture was cooled, diluted with water (200 ml_) and extracted with ethyl acetate (2 x 200 ml_). The combined organic layer was washed with water (100 ml_) and brine (100 ml_), dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (petroleum ether/ethyl acetate, 80/20) to afford the title compound of the title compound as an off-white solid.LC/MS : 269 (M+H)+. 1H NMR (DMSO-d6, 400MHz) delta 8.19 (s, 1 H), 8.18-8.15 (m, 1 H), 7.90-7.80 (m, 1 H), 3.19-3.15 (m, 1 H), 2.90-2.85 (m, 1 H), 2.71 -2.60 (m, 1 H), 1 .81 -1.75 (m, 2H), 1.60-1.31 (m, 3H), 1.31-1.21 (m, 1 H), 0.70 (d, J = 6.4 Hz, 3H).
at 100℃; for 12h; A mixture of 4-fluro 3-trifluro-methylbenzonitrile (5 g, 26.4 mmol) and 2-methylpiperidine (6.25 ml_, 52.9 mmol) was heated at 10O C under N2 for 12h.The reaction mixture was diluted with water (100 ml_) and was extracted with EtOAc (2chi100ml_). The organic layer was washed with water (2chi100mL) and brine solution (10OmL). The solvent was dried over sodium sulphate and concentrated. The residue was purified by flash chromatography using silica-gel (60-120 mesh) and pet-ether /EtOAc as eluent to afford the title compound as an off-white solid. 1H NMR (CDCI3, 400 MHz) delta 7.87 (s, 1 H), 7.71 -7.74 (d, 1 H), 7.50 (bs, 1 H), 2.95-3.03 (m, 2H), 2.49-2.54 (m, 1 H), 1.71 -1 .77 (m, 3H), 1 .58-1.59 (m, 1 H), 1.36-1.39 (m, 2H), 0.75-0.77 (d, 3H). HPLC (Method C) Rt 5.09 min (Purity: 98.8%).
In dimethyl sulfoxide; at 100℃; for 12h;Inert atmosphere; 4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl) benzonitrile <strong>[67515-59-7]4-fluoro-3-(trifluoromethyl)benzonitrile</strong> (Combi-blocks, 50 g; 264.40 mmol) and 2- methylpiperidine (Acros, 156.08 ml 1 321.98 mmol) in DMSO (500 ml_) were heated at 1000C under nitrogen for 12h. After this time, Et2O and water were added to the reaction mixture and organic phase was washed with water, NaHCtheta3 and a saturated aqueous solution of NH4CI successively. Organics were dried over MgSO4, evaporated under vacuum to give the title compound as a beige powder. 1H NMR (DMSO-d6) delta 8.19 (d, J = 2 Hz, 1 H), 8.12 (dd, J = 8.4, 2 Hz, 1 H), 7.75 (d, J = 8.2 Hz, 1 H), 3.15-3.10 (m, 1 H), 2.90-2.85 (m, 1 H), 2.60-2.51 (m, 1 H), 1.77-1.25 (m, 6H), 0.72 (d, J = 6.0 Hz, 3H). LC/MS (Method B): 269.2 (M+H)+.
In dimethyl sulfoxide; at 100℃; for 12h;Inert atmosphere of nitrogen; A mixture of <strong>[67515-59-7]4-fluoro-3-(trifluoromethyl)benzonitrile</strong> (50.0 g, 0.26 mol, Combi-Blocks AN- 1049) and 2-methylpiperidine (156 ml_, 1.32 mol) in DMSO (500 ml.) was heated at 1000C under nitrogen for 12 hours. The reaction mixture was diluted with Et2O and washed with water, a saturated aqueous solution of NaHCO3 and a saturated aqueous solution of NH4CI. The organic layer was dried (MgSO4) and the solvent was removed under reduced pressure to give the title compound as a beige powder. UPLC/MS, M-(ESI): 269.2. 1H NMR (DMSO-d6, 300 MHz) delta 8.19 (d, J=2.0 Hz, 1 H), 8.12 (dd, J=8.4, 2.0 Hz, 1 H), 7.75 (d, J=8.2 Hz, 1 H), 3.13 (m, 1 H), 2.88 (m, 1 H), 2.56 (m, 1 H), 1.77-1.25 (m, 6H), 0.72 (d, J=6.0 Hz, 3H).

 

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