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Chemical Structure| 847157-47-5 Chemical Structure| 847157-47-5

Structure of 847157-47-5

Chemical Structure| 847157-47-5

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Product Details of [ 847157-47-5 ]

CAS No. :847157-47-5
Formula : C9H10INO4S
M.W : 355.15
SMILES Code : O=C(OC)C1=CC(NS(=O)(C)=O)=CC(I)=C1

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Application In Synthesis of [ 847157-47-5 ]

* 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 [ 847157-47-5 ]

[ 847157-47-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 217314-45-9 ]
  • [ 124-63-0 ]
  • [ 847157-47-5 ]
YieldReaction ConditionsOperation in experiment
With pyridine; In dichloromethane; at 0 - 20℃; To a0 C solution of aniline from step B (21.7 g, 78.3 mmol) in 3: 1CECl2 : pyridine (75mL) was added methanesulfonyl chloride (6.36mL, 82.2 mmol). The ice bath was removed after 15 minutes and the solution was. stirred overnight at rt. The reaction mixture was extracted several times with INHC1. <Desc/Clms Page number 47>The organic phase was dried, concentrated, and chromatographed (1: 1 EtOAc: Hex) to afford the desired sulfonamide as a white solid.
With pyridine; In dichloromethane; at 0 - 20℃; Step C: To a 0C solution of aniline from step B (21.7 g, 78.3 mmol) in 3:1 DCM:pyridine (75 mL) wasadded methanesulfonyl chloride (6.36 mL, 82.2 mmol). The ice bath was removed after 15 min and thesolution was stirred overnight at rt. The reaction mixture was extracted several times with IN HC1. Theorganic phase was dried, concentrated, and cliromatographed (1:1 EtOAc:Hex) to afford the desiredsulfonamide as a white solid.
With pyridine; In dichloromethane; at 0 - 20℃; Step C: Mesylation; To a 0 C solution of aniline from step B (21.7 g, 78.3 mmol) in 3:1 1 CH2Cl2: pyridine (75 mL) was added methanesulfonyl chloride (6.36 mL, 82.2 mmol). The ice bath was removed after 15 min and the solution was stirred overnight at rt. The reaction mixture was extracted several times with IN HCI. The organic phase was dried, concentrated, and chromatographed (1:1 EtOAc:Hex) to afford 25.2 g of the desired sulfonamide as a white solid.
With pyridine; In dichloromethane; at 0 - 20℃; Step C: To a 0C solution of the aniline from step B (21.7 g, 78.3 mmol) in 3: 1 CH2CIZ : PYRIDINE (75 mL) was added methanesulfonyl chloride (6.36 ML, 82.2 mmol). The ice bath was removed after 15 minutes and the reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted with EtOAc (200 mL), washed 2x IN HC1, and dried over MGSO4. The solvent was removed in vacuo and the residue was purified by silica gel chromatography (1 : 1 EtOAc/Hexanes) to provide he sulfonamide. LCMS [M+] 355. 8. IH NMR (CDC13) 6 8.17 (s, 1H), 7.86 (s, 1H), 7.18 (s, 1H), 3.95 (s, 3H), 3.08 (s, 3H).

 

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