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Chemical Structure| 191338-94-0 Chemical Structure| 191338-94-0

Structure of 191338-94-0

Chemical Structure| 191338-94-0

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Product Details of [ 191338-94-0 ]

CAS No. :191338-94-0
Formula : C14H18N2O4
M.W : 278.30
SMILES Code : O=C(OCC)C(C1=C(NC(C(C)(C)C)=O)C=CN=C1)=O
MDL No. :MFCD11044174

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Application In Synthesis of [ 191338-94-0 ]

* 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 [ 191338-94-0 ]

[ 191338-94-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 70298-89-4 ]
  • [ 95-92-1 ]
  • [ 191338-94-0 ]
YieldReaction ConditionsOperation in experiment
25.6% To a stirred solution of B (3 g, 16.83 mmol) in dry THF (30 mL) was added n-BuLi (21.5 mL, 50.5 mmol, 2.3M in hexane) dropwise at -78C under an inert atmosphere. After being stirred for 30 min at 0C, a solution of diethyl oxalate (5.6 mL, 42 mmol) in dry tetrahydrofuran (THF) (5.6 mL) was added to reaction mixture at -78C. The resulting reaction mixture was warmed to room temperature (RT) and the stirring was continued for another 2 h. The reaction mixture was diluted with cold water (100 mL) and extracted with diethyl ether (2x20 mL). The combined organic phases were dried over anhydrous sodium sulfate (Na2S04), filtered and concentrated in vacuo. The crude material was purified by silica gel column chromatography eluting with 30% ethyl aceate (EtOAc)/hexane to afford C (1.2g, 25.6%) as a thick syrup. *H NMR (500 MHz, CDC13): delta 11.47 (bs, NH), 8.92 (s, 1H), 8.74 (d, / = 5.5 Hz, 1H), 8.66 (d, / = 5.5 Hz, 1H), 4.51 (q, / = 7.5 Hz, 2H), 1.45 (t, 7 = 7.5 Hz, 3H), 1.36 (s, 9H).
To a solution of compound 13 (5.34 g, 30 mmoi) in TH (200 ml) st - ?8:0C was added dropwise / BuLi (47 ml, 75 mmoi) and the reaction was stirred for 3 hr at -10C. The reaction was cooled to ~78eC and a solution of diethyl oxalate (22 g, 150 mmoi) In THF (20 rnl) was added dropwise and the mixture was stirred overnight at room temperature. NH4CI was added, and the reaction was extracted with EtOAc, washed with brine, dried, concentrated under reduced pressure and purified by flash chromatography (silica gel/EtOAc PE 1 :10-1:8) to give the product 1.4 as a solid. MS: m/z caicd for C14H18N204 278.13, found [M+Hf 279.
 

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