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Chemical Structure| 1357289-08-7 Chemical Structure| 1357289-08-7

Structure of 1357289-08-7

Chemical Structure| 1357289-08-7

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Product Details of [ 1357289-08-7 ]

CAS No. :1357289-08-7
Formula : C20H23NO8
M.W : 405.40
SMILES Code : O=C(C1=C(OCC2=CC=CC=C2)C(C(C(OC)=O)=CN1CC(OC)OC)=O)OC
MDL No. :MFCD28978324

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Application In Synthesis of [ 1357289-08-7 ]

* 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 [ 1357289-08-7 ]

[ 1357289-08-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1246616-66-9 ]
  • [ 22483-09-6 ]
  • [ 1357289-08-7 ]
YieldReaction ConditionsOperation in experiment
91% In toluene; at 100℃; for 3h; Add 10 mol of 4-oxo-3-benzyloxy-4H-pyran-2,5-dicarboxylic acid dimethyl ester obtained in Example 3 to 100 ml of toluene into a reaction flask,Then, the reaction bottle was placed in an oil bath and heated to 100 C. When refluxed, 12 mol of aminoacetaldehyde dimethyl acetal was added dropwise. After the addition, the reflux was continued for 3 h. After the reaction was completed,After cooling to room temperature, the toluene solvent was removed by rotary evaporation, and then the crude product was separated by column chromatography. The eluent was n-hexane: ethyl acetate:methanol = 12:3:2.2,5-pyridinedicarboxylic acid, 1-(2,2-dimethoxyethyl)-1,4-dihydro-4-oxo-3-benzyloxy-2,5-dimethyl ester,The yield was 91%;
88% In methanol; for 6h;Reflux; Aminoacetaldehyde dimethyl acetal (0.72 g, 6.9 mmol) was added dropwise to a methanol (20 mL) slurry solution of compound 12A (2.0 g, 6.3 mmol) at room temperature, and the mixture was then stirred for 6 hours under heating to reflux. After the completion of reaction, the solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate = 3:17 (v/v)) to obtain 2.26 g (yield: 88%) of compound 12B as a colorless oil. 1H-NMR (CDCl3) delta: 3.38 (6H, s), 3.81 (3H, s), 3.91 (2H, d, J = 4.7 Hz), 3.93 (3H, s), 4.47 (1H, t, J = 4.7 Hz), 5.29 (2H, s), 7.29-7.37 (3H, m), 7.42-7.44 (2H, m), 8.15 (1H, s). The compound 12B was dried under conditions of concentration under reduced pressure and left standing at 5C for approximately 2 months. In this case, this compound was still in an oil form and was not crystallized. As a result of various studies, however, the compound was successfully crystallized by repeating the addition of ethyl acetate and concentration and isolated as white crystals.
 

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