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Chemical Structure| 1177421-54-3 Chemical Structure| 1177421-54-3

Structure of 1177421-54-3

Chemical Structure| 1177421-54-3

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Product Details of [ 1177421-54-3 ]

CAS No. :1177421-54-3
Formula : C5H5BrN2O2S
M.W : 237.07
SMILES Code : O=S(C1=CN=C(Br)C=N1)(C)=O
MDL No. :MFCD14702720
InChI Key :AENSXEJTROWUTN-UHFFFAOYSA-N
Pubchem ID :72219279

Safety of [ 1177421-54-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1177421-54-3 ]

* 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 [ 1177421-54-3 ]

[ 1177421-54-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1049026-49-4 ]
  • [ 1177421-54-3 ]
YieldReaction ConditionsOperation in experiment
(107d) 2-Bromo-5-(methylsulfonyl)pyrazine 2,5-Dibromopyrazine (270 mg, 1.14 mmol) was dissolved in tetrahydrofuran (10 mL), and sodium thiomethoxide (320 mg, 4.57 mmol) was added at room temperature, followed by stirring at room temperature for 2.5 hours under nitrogen atmosphere. To this reaction solution, water (10 mL) was added, and extraction was carried out with diethyl ether (10 mL). The organic layer was washed with saturated brine, and subsequently dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified using silica gel column chromatography (elution solvent: ethyl acetate/hexane=5%-10%) to afford a yellow solid. This was dissolved in methylene chloride (10 mL), and m-chloroperbenzoic acid (approximately 65%, 580 mg, approximately 2.2 mmol) was added at room temperature, followed by stirring at room temperature for 1 hour under nitrogen atmosphere. To this reaction solution, a saturated aqueous sodium hydrogencarbonate solution (10 mL) was added, and extraction was carried out with methylene chloride (10 mL). The organic layer was washed with saturated brine, and subsequently dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified using silica gel column chromatography (elution solvent: ethyl acetate/hexane=15%-25%) to afford the desired compound (190 mg, yield 70%) as a white solid. 1H-NMR (CDCl3, 400 MHz): delta 3.26 (3H, s), 8.80 (1H, d, J=1.2 Hz), 9.06 (1H, d, J=1.2 Hz).
With Oxone; In water; at 20℃; for 3.0h; Step B: 2-bromo-5-(methylsulfonyl)pyrazine: An aqueous solution of Oxone (4.0 g, 6.6 mmol,3.13 mL) was added dropwise to a methanol solution of <strong>[1049026-49-4]2-bromo-5-(methylsulfanyl)pyrazine</strong>(450 mg, 2.2 mmol, 19 mL) at ambient temperature. The reaction mixture was stirred for 3hours, filtered over a pad of CELITE and then organic layer was concentrated in vacuo. The crude residue was purified via MPLC (0-100% EtOAc/hexane gradient) to afford titlecompound.
 

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