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Structure of 941585-25-7

Chemical Structure| 941585-25-7

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Product Details of [ 941585-25-7 ]

CAS No. :941585-25-7
Formula : C8H15NO2S
M.W : 189.28
SMILES Code : O=C(N1CC(S)C1)OC(C)(C)C
MDL No. :MFCD01861743
InChI Key :GUZYDTTYVXLGCV-UHFFFAOYSA-N
Pubchem ID :58513580

Safety of [ 941585-25-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 941585-25-7 ]

* 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 [ 941585-25-7 ]

[ 941585-25-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 327056-62-2 ]
  • [ 941585-25-7 ]
  • tert-butyl 3-((6-cyanopyridin-3-yl)thio)azetidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
To a mixture of tert-butyl 3-mercaptoazetidine-l-carboxylate (8 g, 42.27 mmol) in DMF (50 mL) was added NaH (2.03 g, 50.72 mmol, 60% purity) in portions at 0 C under nitrogen. The mixture was stirred at 25 C for 30 min, then 5-fluoropyridine-2-carbonitrile (5.16 g, 42.27 mmol) in DMF (10 mL) was added slowly and the mixture was stirred at 25 C for 2 h. The mixture was diluted with H2O (500 mL) and the mixture was extracted with EtOAc. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography to give tert-butyl 3-((6- cyanopyridin-3-yl)thio)azetidine-l-carboxylate (7 g, crude).
 

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