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Chemical Structure| 104797-47-9 Chemical Structure| 104797-47-9

Structure of 104797-47-9

Chemical Structure| 104797-47-9

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Product Details of [ 104797-47-9 ]

CAS No. :104797-47-9
Formula : C14H10N4O3S3
M.W : 378.45
SMILES Code : O=C(SC1=NC2=CC=CC=C2S1)/C(C3=CSC(N)=N3)=N\OC(C)=O
MDL No. :MFCD09031340

Safety of [ 104797-47-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302+H312-H315-H318-H411
Precautionary Statements:P273-P280-P301+P312+P330-P302+P352+P312-P305+P351+P338+P310
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 104797-47-9 ]

* 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.

  • Upstream synthesis route of [ 104797-47-9 ]
  • Downstream synthetic route of [ 104797-47-9 ]

[ 104797-47-9 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 104797-47-9 ]
  • [ 79349-82-9 ]
  • [ 91832-40-5 ]
YieldReaction ConditionsOperation in experiment
88.6%
Stage #1: With triethylamine In tetrahydrofuran at 20 - 23℃; for 5 h;
Stage #2: With hydrogenchloride; methoxybenzene In tetrahydrofuran; dichloromethane at -25 - -20℃; for 1.5 h;
In a dry reaction flask, add 22.6g 7-AVCA, 43g cefdinir side chain active ester and 150 ml tetrahydrofuran. Control temperature 20 °C-23 °C. Add dropwise 12g triethylamine. Stir the reaction for 5h. HPLC measured end point of the reaction. After the reaction is complete, add 200 ml dichloromethane, anisole 30 ml. Cool to -25 °C- -20 °C. Place the dry hydrogen chloride gas. After about 1.5h, HPLC measured end point of the reaction. After the reaction, through N2In the system away excess hydrogen chloride gas, the temperature of not more than 0 °C, dropwise 5percent of K2CO3, Control pH value is 5.5 - 6.0, layered, in the aqueous phase by adding 80mLCH2Cl2Extraction, layered, in the aqueous phase by adding 2g activated carbon to decolorize 1h, filtering, adding water 400 ml, for 2 mol/L hydrochloric acid to adjust the pH value to 2.2 - 2.4, temperature control 25 °C -28 °C, nourishing crystal 2h after filtering, washing, alcohol washing, drying, to obtain cefdinir 35g, yield 88.6percent, purity of 99.2percent.
References: [1] Patent: CN106279207, 2017, A, . Location in patent: Paragraph 0033; 0034; 0035.
[2] Patent: WO2005/121154, 2005, A1, . Location in patent: Page/Page column 10.
[3] Patent: WO2006/117794, 2006, A1, . Location in patent: Page/Page column 4-5.
  • 2
  • [ 104797-47-9 ]
  • [ 91832-40-5 ]
References: [1] Synthetic Communications, 2007, vol. 37, # 13, p. 2275 - 2283.
 

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