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Chemical Structure| 142137-18-6 Chemical Structure| 142137-18-6

Structure of 142137-18-6

Chemical Structure| 142137-18-6

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Product Details of [ 142137-18-6 ]

CAS No. :142137-18-6
Formula : C6H6BrNS
M.W : 204.09
SMILES Code : CSC1=CN=CC(Br)=C1
MDL No. :MFCD08689537

Safety of [ 142137-18-6 ]

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

Application In Synthesis of [ 142137-18-6 ]

* 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.

  • Downstream synthetic route of [ 142137-18-6 ]

[ 142137-18-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 142137-18-6 ]
  • [ 445491-71-4 ]
YieldReaction ConditionsOperation in experiment
82% With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; d 3-Bromo-5-methanesulfonyl-pyridine MCPBA (9.2 g, 38 mmol) was added slowly to a solution of 3-bromo-5-methylsulfanyl-pyridine (3.8 g, 19 mmol) in dichloromethane (50 mL). After stirring for 30 minutes, the reaction was diluted with dichloromethane and quenched carefully with 1N NaOII. The product was extracted with dichloromethane and dried over magnesium sulfate. The solvent was removed under reduced pressure to give title compound (2.7 g, 82% yield) as a white solid.
47% With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20℃; for 0.5h; To a solution of 3-bromo-5-methanesulfanyl-pyridine (8.80 g, 43 mmol) in CH2Cl2 was treated slowly portionwise with 3-chloroperbenzoic acid (21.26 g, 86 mmol) at rt (exothermic reaction). The reaction mixture was stirred for 30 minutes at rt under Argon, then diluted with an additional portion of CH2Cl2 and washed with 1N NaOH solution. The aqueous layer was extracted with 3 portions of CH2Cl2 and the combined layers were dried over MgSO4, filtered and concentrated to give the title compound (4.75 g, 47%) as a white solid. MS (ISP) 236.1 [(M+H)+], 237.9[(M+2+H)+].
With Oxone; sodium hydrogencarbonate; In tetrahydrofuran; methanol; water; at 20℃; for 4.0h; To 3,5-dibromopyridine (2.96 g, 12.5 mmol) in diethyl ether (70 ml) at -78 C. was added n-butyllithium 1.6M in hexanes (8.6 ml, 13.7 mmol) and the resulting mixture was stirred in the cold for 3 hours. Dimethyl disulfide (1.12 ml, 12.5 mmol) was added and the mixture was warmed to room temperature, then partitioned between ether and water. To the crude product from evaporation of the organic phase was added tetrahydrofuran (80 ml), methanol (20 ml), oxone (17 g) and enough saturated aqueous sodium bicarbonate to afford a slightly basic medium. After stirring for 4 hours at room temperature, an excess of 1M aqueous sodium metabisulfite was added, the organic solvents were evaporated, and the residue was partitioned between ethyl acetate and water. The crude product from the organic phase was stirred in a small volume of ethyl acetate and filtered to afford the 3-Bromo-5-methylsulfonylpyridine compound as a solid.
With Oxone; In tetrahydrofuran; water; at 0 - 20℃; Step 2) Formation of 3-bromo-5-(methylsulfonyl)pyridineTo a solution of 2-bromo-6-(methylthio)pyridine (10 g, 49.0 mmol) in THF (125 mL) was added oxone (30 g, 98.0 mmol) in water in a dropwise fashion at 00C and stirred at RT for 3 h. The mixture was extracted with EtOAc washed with water, brine, dried over Na2SO4, evaporated and purified by silica gel column chromatography (PE/EtOAc) to afford the title compound as a white solid. LC/MS, M+(ESI): 237.8.HPLC, Rt: 5.45 min (purity: 99.6%). 1H NMR (DMSO-d6, 400 MHz) delta 9.07-9.04 (m, 2H), 8.58 (s, 1 H), 3.39 (s, 3H).

 

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