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Chemical Structure| 2323-17-3 Chemical Structure| 2323-17-3

Structure of 2323-17-3

Chemical Structure| 2323-17-3

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Product Details of [ 2323-17-3 ]

CAS No. :2323-17-3
Formula : C7H12OS
M.W : 144.23
SMILES Code : O=C1CC(SC(C1)C)C
MDL No. :MFCD24688787

Safety of [ 2323-17-3 ]

Application In Synthesis of [ 2323-17-3 ]

* 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 [ 2323-17-3 ]

[ 2323-17-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2323-17-3 ]
  • [ 1065181-58-9 ]
  • [ 1065182-49-1 ]
YieldReaction ConditionsOperation in experiment
26% Intermediate 59:Ethyl S-bromo-S^jtheta-dimethyltetrahydro^H-thiopyran^-ylJ-IH-indole-y-carboxylate.2,6-Dimethyltetrahydro-4H-thiopyran-4-one (0.293g, 2.03mmol) was dissolved in dichloromethane (35ml_) in an oven dried flask containing 3 A molecular sieves and stirred under argon at 0 0C. TMS-OTf (0.451 g, 2.03mmol, 0.36 ml.) was added slowly to the mixture over 10 min. Ethyl 5-bromo-1 /-/-indole-7-carboxylate (0.293g, 2.031 mmol) was dissolved in DCM (1OmL) and added to the reaction via syringe pump over 2 hours, after which it was stirred for 3 hours between 0 and 10 0C. The reaction was cooled to 0 0C and triethylsilane (0.353 g, 0.485 ml_, 3.04 mmol) was then added all at once and the reaction was stirred at room temperature overnight. The reaction was then quenched with a saturated sodium bicarbonate solution, filtered, then extracted with DCM. The combined organics were washed with water. The combined aqueous layers were back-extracted with DCM. The combined organics were washed with brine, dried with MgSO4, and concentrated. The crude compound was purified on Combiflash silica column with 0-30% EA/DCM to give 0.212g (26%) of the the title compound. LC/MS: m/z 397 (M+H), Rt 1.51 min.
 

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