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Chemical Structure| 2925-55-5 Chemical Structure| 2925-55-5

Structure of 2925-55-5

Chemical Structure| 2925-55-5

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Product Details of [ 2925-55-5 ]

CAS No. :2925-55-5
Formula : C9H5ClFNO2S
M.W : 245.66
SMILES Code : O=S(C1=C2N=CC(F)=CC2=CC=C1)(Cl)=O

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Application In Synthesis of [ 2925-55-5 ]

* 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 [ 2925-55-5 ]

[ 2925-55-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 396-31-6 ]
  • [ 2925-55-5 ]
YieldReaction ConditionsOperation in experiment
With chlorosulfonic acid; at 130℃; A mixture of <strong>[396-31-6]3-fluoroquinoline</strong> (0.6 g, 4.08 mmol) and HSO3CI (2 mL) in a round bottom flask equipped with a cooling condenser was stirred at 130C overnight. When TLC indicated that the reaction was complete, the resulting mixture was carefully poured into crushed ice, the mixture was extracted with DCM (100 mL x 3), and the combined organic layers were dried over Na2S04, and concentrated. The crude mixture was purified by chromatography (5% Ethyl Acetate/PE) to give the desired 3- fluoroquinoline-8-sulfonyl chloride. 1H NMR (CHLOROFORM-d) δ: 9.15 (d, J = 2.6 Hz, 1H), 8.53 (d, J = 7.6 Hz, 1H), 8.23 (dd, J = 8.2, 0.9 Hz, 1H), 7.97 (dd, J = 8.1, 2.8 Hz, 1H), 7.69 - 7.83 (m, 1H). LC-MS: m/z 246.7 (M+H)+
With chlorosulfonic acid; at 130℃; A mixture of <strong>[396-31-6]3-fluoroquinoline</strong> (0.6 g, 4.08 mmol) and HSO3Cl (2 mL) in a round bottom flask equipped with a cooling condenser was stirred at 130 C. overnight. When TLC indicated that the reaction was complete, the resulting mixture was carefully poured into crushed ice, the mixture was extracted with DCM (100 mL×3), and the combined organic layers were dried over Na2SO4, and concentrated. The crude mixture was purified by chromatography (5% Ethyl Acetate/PE) to give the desired <strong>[396-31-6]3-fluoroquinoline</strong>-8-sulfonyl chloride. 1H NMR (CHLOROFORM-d) δ: 9.15 (d, J=2.6 Hz, 1H), 8.53 (d, J=7.6 Hz, 1H), 8.23 (dd, J=8.2, 0.9 Hz, 1H), 7.97 (dd, J=8.1, 2.8 Hz, 1H), 7.69-7.83 (m, 1H). LC-MS: m/z 246.7 (M+H)+
With chlorosulfonic acid; at 130℃; A mixture of <strong>[396-31-6]3-fluoroquinoline</strong> (0.6 g, 4.08 mmol) and HSO3CI (2 mL) in a round bottom flask equipped with a cooling condenser was stirred at 130C overnight. When TLC indicated that the reaction was complete, the resulting mixture was carefully poured into crushed ice, the mixture was extracted with DCM (100 mL x 3), and the combined organic layers were dried over Na2S04, and concentrated. The crude mixture was purified by chromatography (5% Ethyl Acetate/PE) to give the desired 3- fluoroquinoline-8-sulfonyl chloride. 1H NMR (CHLOROFORM-d) δ: 9.15 (d, J = 2.6 Hz, 1H), 8.53 (d, J = 7.6 Hz, 1H), 8.23 (dd, J = 8.2, 0.9 Hz, 1H), 7.97 (dd, J = 8.1, 2.8 Hz, 1H), 7.69 - 7.83 (m, 1H). LC-MS: m/z 246.7 (M+H)+
 

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