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Chemical Structure| 1562692-35-6 Chemical Structure| 1562692-35-6

Structure of 1562692-35-6

Chemical Structure| 1562692-35-6

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Product Details of [ 1562692-35-6 ]

CAS No. :1562692-35-6
Formula : C13H9ClF3NO2S
M.W : 335.73
SMILES Code : NC1=CC=C(S(=O)(C2=CC=C(Cl)C(C(F)(F)F)=C2)=O)C=C1

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Application In Synthesis of [ 1562692-35-6 ]

* 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 [ 1562692-35-6 ]

[ 1562692-35-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 61929-24-6 ]
  • [ 1562692-35-6 ]
  • 4-(4-((4-chloro-3-(trifluoromethyl)phenyl)sulfonyl)phenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione [ No CAS ]
YieldReaction ConditionsOperation in experiment
8% With toluene-4-sulfonic acid; In isopropyl alcohol; at 80℃; for 4h; To the mixture of A-5 (100 g, 298 mmol) in isopropanol (1.20 L) was added 2-bromo-l,3,4-thiadiazole (49.2 g, 298 mmol) and TsOHH20 (8.50 g, 44.7 mmol). The mixture was stirred at 80C for 4 hrs. The mixture was filtered, and the filtrate was evaporated to give a crude product. The crude product was purified by column (0272) chromatography on silica gel (petroleum ether/ethyl acetate = 3/1-0/1, 0-10% 0.5M (0273) H3 H20/MeOH in DCM) to give a yellow solid which was made a slurry from MeOH (300 mL), MTBE (500 mL), and H20 (500 mL), then dried in vacuum to give Compound 1 (20 g, 8% yield) as a white solid. 1H MR (500 MHz, DMSO-d6) delta 14.07 (s, 1H), 8.77 (s, 1H), 8.42 - 8.32 (m, 2H), 8.32 - 8.25 (m, 2H), 8.03 (dd, J = 8.8, 2.3 Hz, 3H). LCMS ES+ (m/z), 420.0 (M+l)+, Cl pattern found.
8% With toluene-4-sulfonic acid; In isopropyl alcohol; at 80℃; for 4h; Step 5 : To the mixture of A-5 (100 g, 298 mmol) in isopropanol (1.20 L) was added 2-bromo-l,3,4-thiadiazole (49.2 g, 298 mmol) and TsOH H20 (8.50 g, 44.7 mmol). The mixture was stirred at 80C for 4 hrs. The mixture was filtered, and the filtrate was evaporated to give a crude product. The crude product was purified by column (0593) chromatography on silica gel (petroleum ether/ethyl acetate = 3/1-0/1, 0-10% 0.5M (0594) NH3 H20/MeOH in DCM) to give a yellow solid which was made a slurry from MeOH (300 mL), MTBE (500 mL), and H20 (500 mL), then dried in vacuum to give Compound 1 (20 g, 8% yield) as a white solid. 1H NMR (500 MHz, DMSO-d6) d 14.07 (s, 1H), 8.77 (s, 1H), 8.42 - 8.32 (m, 2H), 8.32 - 8.25 (m, 2H), 8.03 (dd, J = 8.8, 2.3 Hz, 3H). LCMS ES+ (m/z), 420.0 (M+l)+, Cl pattern found
 

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