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Chemical Structure| 61714-77-0 Chemical Structure| 61714-77-0

Structure of 61714-77-0

Chemical Structure| 61714-77-0

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Product Details of [ 61714-77-0 ]

CAS No. :61714-77-0
Formula : C5H4ClNO4S2
M.W : 241.67
SMILES Code : O=S(C1=CC([N+]([O-])=O)=C(C)S1)(Cl)=O
MDL No. :MFCD18838720

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Application In Synthesis of [ 61714-77-0 ]

* 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 [ 61714-77-0 ]

[ 61714-77-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 61714-77-0 ]
  • [ 1597-32-6 ]
  • N-(6-fluoropyridin-2-yl)-5-methyl-4-nitrothiophene-2-sulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% With pyridine; In dichloromethane; at 20℃; for 72h; Step 1. Preparation of N-(6-fluoropyridin-2-yl)-5-methyl-4-nitrothiophene-2-sulfonamide To a solution of 5-methyl-4-nitrothiophene-2-sulfonyl chloride (0.500 g, 2.07 mmol) and 2-amino 6-fluoropyridine (0.256 g, 2.28 mmol) in dichloromethane (11 mL) was added pyridine (0.25 mL, 3.1 mmol). The reaction mixture was stirred at ambient temperature for 72 hours. The reaction mixture was diluted with dichloromethane (10 mL) and water (10 mL). The layers were separated and the aqueous phase was extracted with dichloromethane (3*10 mL).
71% With pyridine; In dichloromethane; at 20℃; for 72h; To a solution of 5-methyl-4-nitrothiophene-2-sulfonyl chloride (0.500 g, 2.07 mmol) and 2-amino 6-fluoropyridine (0.256 g, 2.28 mmol) in dichloromethane (11 mL) was added pyridine (0.25 mL, 3.1 mmol). The reaction mixture was stirred at ambient temperature for 72 hours. The reaction mixture was diluted with dichloromethane (10 mL) and water (10 mL). The layers were separated and the aqueous phase was extracted with dichloromethane (3 c 10 mL). The combined organic phases were washed with a solution of 5% hydrochloric acid (3 x 10 mL) and brine (10 mL), dried over anhydrous magnesium sulfate, and filtered. Concentration of the filtrate in vacuo and purification of the residue by column chromatography, eluting with a gradient of 10 to 80% of ethyl acetate in hexanes, afforded the title compound as a yellow oil (0.465 g, 71 % yield): MS (ES-) m/z 316.0 (M - 1).
 

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