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Chemical Structure| 612532-09-9 Chemical Structure| 612532-09-9

Structure of 612532-09-9

Chemical Structure| 612532-09-9

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Product Details of [ 612532-09-9 ]

CAS No. :612532-09-9
Formula : C17H26N2O2
M.W : 290.41
SMILES Code : NC(C1CCN(C(OC(C)(C)C)=O)CC1)C2=CC=CC=C2
MDL No. :MFCD12912652

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Application In Synthesis of [ 612532-09-9 ]

* 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 [ 612532-09-9 ]

[ 612532-09-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 193217-39-9 ]
  • [ 612532-09-9 ]
YieldReaction ConditionsOperation in experiment
90% Synthesis of tert-butyl 4-(amino(phenyl)mefhyl)piperidine-l-carboxylate½r/-butyl 4-benzoylpiperidine-l-carboxylate (484 mg, 1.67 mmol) was dissolved in MeOH (15mL) and then NH4OAc (1.54 g, 20 mmol) was added. Reaction was stirred for 10 minutes at 25 C. NaCNBH3 (420 mg, 6.68 mmol) was then added and the reaction was heated to 60 C and stirred at that temperature for 16 hours. The solvent was removed under reduced pressure and the reaction mixture was suspended in 0.5 M NaOH (75 mL). Extracted with EtOAc (3 x 20 mL) and then dried with MgS04 and then under reduced pressure to give the title compound: clear oil (435 mg, 90%) NMR (400 MHz, CHLOROFORM-d) δ ppm 7.33 (m, .7=7.30 Hz, 2 H), 7.28 (d, 7=4.77 Hz, 3 H), 4.19 (br. s, 1 H), 4.02 (br. s, 1 H), 3.62 (d, 7=7.78 Hz, 1 H), 2.62 - 2.74 (m, 1 H), 2.48 - 2.61 (m, 1 H), 1.93 (d, 7=12.55 Hz, 1 H), 1.50 - 1.69 (m, 4 H), 1.44 (s, 9 H), 1.25 - 1.33 (m, 1 H), 1.00 - 1.14 (m, 1 H)
40% To a solution of tert-butyl 4-benzoylpiperidine-l-carboxylate (0.188 g, 0.65 mmol) in MeOH (5 mL) was added ammonium acetate (0.6 g, 7.8 mmol). The reaction was stirred for 10 minutes at 25 C, then sodium cyanoborohydride (0.163g, 2.59 mmol) was added. The reaction heated to 60 C for 16 hours. The reaction completion was monitored by TLC and the reaction was quenched with 0.5N NaOH solution and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried using Na2S04 and concentrated under reduced pressure to a residue which was purified by column chromatography to obtain tert-butyl 4-(amino(phenyl)methyl)piperidine-l- carboxylate (0.2g, 40%) . LCMS: m/z = 190.3 (M+H) +.
 

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