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Chemical Structure| 1392429-92-3 Chemical Structure| 1392429-92-3

Structure of 1392429-92-3

Chemical Structure| 1392429-92-3

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Product Details of [ 1392429-92-3 ]

CAS No. :1392429-92-3
Formula : C9H10F2INO2S
M.W : 361.15
SMILES Code : CCCS(=O)(NC1=CC=C(F)C(I)=C1F)=O
MDL No. :MFCD32196966

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Application In Synthesis of [ 1392429-92-3 ]

* 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 [ 1392429-92-3 ]

[ 1392429-92-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1145881-54-4 ]
  • [ 1392429-92-3 ]
  • 2
  • [ 10147-36-1 ]
  • [ 1437316-91-0 ]
  • [ 1392429-92-3 ]
YieldReaction ConditionsOperation in experiment
83% With pyridine; In 1,2-dichloro-ethane; for 2.0h;Reflux; N-(2,4-difluoro-3-iodophenyl)propane-l -sulfonamideTo a solution of <strong>[1437316-91-0]2,4-difluoro-3-iodoaniline</strong> (255mg, lmmol) in 1,2-dichloroethane (3 mL) was added pyridine (lmL), followed by propane- 1-sulfonyl (157mg, 1. lmmol) and the resulting reaction mixture was heated to refluxing for 2 hrs. The solvent was removed in vacuo. The residue was dissolved in EtOAc, washed with aqueous NaHC03, brine, dried over Na2S04, filtered and concentrated in vacuo to afford the desired product (298mg, 83%>).1H NMR (CDCI3): ? 7.56-7.58 (1H, m), 6.90-6.95 (1H, m), 6.44 (1H, br), 3.03-3.07 (2H, m),1.84-1.90 (2H, m), 1.03-1.07 (3H, m).
83% With pyridine; In 1,2-dichloro-ethane; for 2.0h;Reflux; To a solution of <strong>[1437316-91-0]2,4-difluoro-3-iodoaniline</strong> (255 mg, 1 mmol) in 1,2_dichloroethane (3 mL) was slowly added dropwise a solution of P to pyridine (lmL), propylsulfonyl chloride (157 mg, 1. lmmol). The reaction solution was heated under reflux for 2 hours, cooled and concentrated in vacuo to remove the solvent. The resulting oil was dissolved in ethyl acetate (20 mL) and washed with 5% sodium bicarbonate solution, water and saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give N- (2,4-difluoro-3- Iodophenyl) propane-1-sulfonamide (298 mg, 83%).
 

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