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Chemical Structure| 87120-79-4 Chemical Structure| 87120-79-4

Structure of 87120-79-4

Chemical Structure| 87120-79-4

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Product Details of [ 87120-79-4 ]

CAS No. :87120-79-4
Formula : C17H25N3O4
M.W : 335.40
SMILES Code : O=C(N1CCC(NCC2=CC=CC=C2[N+]([O-])=O)CC1)OC(C)(C)C
MDL No. :MFCD14156034

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Application In Synthesis of [ 87120-79-4 ]

* 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 [ 87120-79-4 ]

[ 87120-79-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 79099-07-3 ]
  • [ 24835-08-3 ]
  • [ 87120-79-4 ]
YieldReaction ConditionsOperation in experiment
31. tert-Butyl 4-r(2-nitrobenzyl)amino1piperidine- 1 -carboxylate; To a mixture of <strong>[24835-08-3]2-nitrobenzylamine hydrochloride</strong> (20.0 g, 106.0 mmol) in DCE (250 mL) is added TEA (10.73 g, 106.0 mmol). The mixture is allowed to stir at rt for 5 min. To this mixture N-Boc-4-piperidone (21.13 g, 106.0 mmol), and HOAC (7.96 g, 132.5 mmol), is added and stirred at rt for another 5 min. NaBH(OAc)3 (25.28 g, 119.3 mmol) is added in portions and the mixture is stirred at rt for 1 hr before it is washed with 10 % Na2CO3 solution (100 mL x 3) and brine (50 mL x 2). The organic phase is dried over Na2SO4. The solvent is removed in vacuo to afford the title compound as a red oil, which is used without further purification in subsequent steps.
18. tert-Butyl 4-r(2-nitrobenzyl)aminolρiρeridine-l -carboxvlate; To a mixture of <strong>[24835-08-3]2-nitrobenzylamine hydrochloride</strong> (20.0 g, 106.0 mmol) in DCE (250 mL) is added TEA (10.73 g, 106.0 mmol). The mixture is allowed to stir at rt for 5 min. To this mixture N-Boc-4-piperidone (21.13 g, 106.0 mmol), and HOAC (7.96 g, 132.5 mmol), is added and stirred at rt for another 5 min. NaBH(OAc)3 (25.28 g, 119.3 mmol) is added in portions and the mixture is stirred at rt for 1 hr before it is washed with 10 % Na2CO3 solution (100 mL * 3) <n="59"/>and brine (50 mL x 2). The organic phase is dried over Na2SCU- The solvent is removed in vacuo to afford the title compound as a red oil, which is used without further purification in subsequent steps.
 

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