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Chemical Structure| 849203-09-4 Chemical Structure| 849203-09-4

Structure of 849203-09-4

Chemical Structure| 849203-09-4

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Product Details of [ 849203-09-4 ]

CAS No. :849203-09-4
Formula : C16H25NO5
M.W : 311.37
SMILES Code : O=C(C(CCC12CCN(C(OC(C)(C)C)=O)CC2)C1=O)OC
MDL No. :MFCD20527510

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Application In Synthesis of [ 849203-09-4 ]

* 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 [ 849203-09-4 ]

[ 849203-09-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 849203-09-4 ]
  • [ 191805-29-5 ]
YieldReaction ConditionsOperation in experiment
With lithium hydroxide; In tetrahydrofuran; ethanol; water; at 90℃; for 60h; To a solution of tert-butyl 2-(methoxycarbonyl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylate (17.2 g, 0.055 mol) from Step F in a 2:2:1 mixture of ethanol/tetrahydrofuran/water (555 mL) was added pulverized lithium hydroxide (26 g, 1.10 mol). The reaction mixture was heated to 90 C. for 60 h. The reaction mixture was allowed to cool and was then concentrated, dissolved in water and dichloromethane, and extracted three times with dichloromethane. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and concentrated to afford 11.4 g. The residue was purified by flash chromatography eluting with 20-30% ethyl acetate in hexanes to give the title compound (9.41 g). 1H NMR (400 MHz, CDCl3): delta 1.29-1.37 (m, 2 H), 1.47 (s, 9 H), 1.62-1.69 (m, 2 H), 1.92-1.95 (m, 4 H), 2.30-2.34 (m, 2 H), 3.05-3.10 (m, 2 H), 3.87-3.92 (m, 2 H).
With lithium hydroxide; In tetrahydrofuran; ethanol; water; at 90℃; for 60h; Pulverized lithium hydroxide (26 g, 1.10 mol) was added to a solution of (&S)-8-(l,l-dimethylethyl) 2- methyl l-oxo-8-azaspiro[4.5]decane-2,8-dicarboxylate (Description 51, 17.2 g, 0.055 mol) in ethanol/THF/water (2:2:1, 555 mL) and the mixture was stirred at 90 0C for 60 h. The mixture was cooled and the solvent was evaporated under reduced pressure. Water was added and the mixture was EPO <DP n="30"/>extracted with CH2Cl2 (3x). The combined organic fractions were washed with brine, dried (Na2SO4), filtered, and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography, eluting with 20-30% EtOAc in hexanes, to give the title compound (9.41 g). 1H NMR (400MHz, CDCl3) delta 1.29-1.37 (m, 2H), 1.47 (s, 9H), 1.62-1.69 (m, 2H), 1.92-1.95 (m, 4H), 2.30-2.34 (m, 2H), 3.05-3.10 (m, 2H), 3.87-3.92 (m, 2H).
 

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