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Chemical Structure| 193631-86-6 Chemical Structure| 193631-86-6

Structure of 193631-86-6

Chemical Structure| 193631-86-6

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Product Details of [ 193631-86-6 ]

CAS No. :193631-86-6
Formula : C9H12N2Si
M.W : 176.29
SMILES Code : C[Si](C#CC1=NC=CC=N1)(C)C

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Application In Synthesis of [ 193631-86-6 ]

* 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 [ 193631-86-6 ]
  • Downstream synthetic route of [ 193631-86-6 ]

[ 193631-86-6 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 193631-86-6 ]
  • [ 37972-24-0 ]
YieldReaction ConditionsOperation in experiment
68.8% With tetrabutyl ammonium fluoride In tetrahydrofuran for 0.05 h; To a solution of 3 (3.2g, 18 l5mmol) in IOmLTHF was added IM of TBAF (18.l5mL,i8.i5rnrnoi over 3 minutes. TLC showed the starting material was consumed. The reactionmixture was then concentrated in vacuo. The crude product was purified by silica gel column chromatography to give product 4 (1 .3 g, yield: 68.8percent).LCMS: ith. 105 (M÷H).
67.4% With tetrabutyl ammonium fluoride In tetrahydrofuran for 0.05 h; To a solution of 3.0g, 17.O2mmoi) in iOmL THE was added IM of TBAF over 3 minutes. TLC showed the starting material was consumed. The reaction mixture was then concentrated in vacuo. The crude product was purified by silica gel column chromatography to give product4(1.2 g, yield: 67.4percent).LCMS: m/, 105 (M+HY.
References: [1] Patent: WO2017/173604, 2017, A1, . Location in patent: Page/Page column 17; 18.
[2] Patent: WO2017/117708, 2017, A1, . Location in patent: Page/Page column 18.
[3] Carbohydrate Research, 2011, vol. 346, # 9, p. 1083 - 1092.
[4] MedChemComm, 2019, vol. 10, # 2, p. 263 - 267.
  • 2
  • [ 193631-86-6 ]
  • [ 54-42-2 ]
  • [ 37972-24-0 ]
References: [1] Patent: US5645985, 1997, A, .
 

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