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Chemical Structure| 6967-89-1 Chemical Structure| 6967-89-1

Structure of 6967-89-1

Chemical Structure| 6967-89-1

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Product Details of [ 6967-89-1 ]

CAS No. :6967-89-1
Formula : C11H9NS
M.W : 187.26
SMILES Code : S=C(C1=CC=C2C=CC=CC2=C1)N
MDL No. :MFCD01571356

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Application In Synthesis of [ 6967-89-1 ]

* 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 [ 6967-89-1 ]

[ 6967-89-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2243-82-5 ]
  • [ 6967-89-1 ]
YieldReaction ConditionsOperation in experiment
64% With Lawessons reagent; In tetrahydrofuran; for 3h;Reflux; General procedure: Thioamides 8a-d were prepared from the corresponding amides 7a-d (3 mmol) in the presence of Lawesson's reagent (3.4 mmol) in dry THF (25 mL) under reflux for 3 h. After evaporation of solvent, the crude was partitioned between H2O (20 mL) and CH2Cl2 (20 mL) and the aqueous phase was extracted with CH2Cl2 (3 * 50 mL). The collected solutions were dried over Na2SO4 and evaporated. The residue was purified on silica gel column chromatography in specific condition below reported for each compound.
With Lawessons reagent; In tetrahydrofuran; at 23℃; for 1h; General procedure: Amides (1 mmol) and Lawesson's reagent (490 mg, 1.2 mmol) were added to dry THF (15 mL). The reaction mixture was stirred at room temperature for 1 h, or heated under reflux for 5 h in the case of the 4-nitro derivative. The solvent was evaporated under reduced pressure and the residue was partitioned between aq NaHCO3 (25 mL) and ethyl acetate (25 mL). The organic solvent was separated and dried over anhydrous MgSO4. The crude product was further purified by silica gel flash chromatography, using hexane-ethyl acetate (4:1), to yield the corresponding thioamides as yellow solids (42-60%). 4-Nitrothioamide (2ff),38 4-cyanothiobenzamide (2gg)39 and 3-cyanothiobenzamide (2hh),40 3-methoxythiobenzamide (2ii)41 have been previously reported.
With Lawessons reagent; In tetrahydrofuran;Reflux; General procedure: The mixture of the corresponding amide (0.2 mmol) and Lawesson?s reagent (0.3 mmol) in tetrahydrofuran 4 mL was refluxed and the reaction was monitored by thin layer chromatography (TLC). After the reaction was complete, the crude product was puried by silica-gel column chromatography using ethyl acetate/hexane as eluent solvent system. The pure product was obtained and identified.
 

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