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Chemical Structure| 362703-35-3 Chemical Structure| 362703-35-3

Structure of 362703-35-3

Chemical Structure| 362703-35-3

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Product Details of [ 362703-35-3 ]

CAS No. :362703-35-3
Formula : C13H24N2O4
M.W : 272.34
SMILES Code : COC(=O)C1(CN)CCN(CC1)C(=O)OC(C)(C)C
MDL No. :MFCD07784122

Safety of [ 362703-35-3 ]

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

Application In Synthesis of [ 362703-35-3 ]

* 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 [ 362703-35-3 ]

[ 362703-35-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 362703-34-2 ]
  • [ 362703-35-3 ]
YieldReaction ConditionsOperation in experiment
81% With hydrogen;platinum(IV) oxide; In ethyl acetate; under 2585.81 Torr; for 2.0h; A solution of the piperidine (1.07 g, 3.98 mmol) from reaction (24b) and a catalytic amount of platinum oxide in acetic acid (20 mL) was pressurized with 50 psi of hydrogen for 2 hr. The mixture was filtered through Celite and concentrated. The residue was dissolved in ethyl acetate (20 mL) and washed with saturated sodium bicarbonate solution (2×20mL) and brine (2×20 mL). The organic layer was dried and concentrated to give the desired amine (880 mg, 81%). MS found: (M+H)+=273.
60% With hydrogen; nickel; triethylamine; In methanol; under 2068.65 Torr; To a solution of intermediate 3 (10 g, 37.3 mmol) and triethylamine (1 mL) in MeOH (200 mL) was added Raney-Ni carefully. The resulting mixture was hydrogenated (40 psi H2) overnight. The reaction was filtered through celite, concentrated under vacuum, and purified by preparative HPLC to give intermediate 4 (6 g, 60% yield) as a colorless oil.
 

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