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Chemical Structure| 790263-62-6 Chemical Structure| 790263-62-6

Structure of 790263-62-6

Chemical Structure| 790263-62-6

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Product Details of [ 790263-62-6 ]

CAS No. :790263-62-6
Formula : C10H14ClN3O4S
M.W : 307.75
SMILES Code : O=S(C1=CC=C(Cl)C([N+]([O-])=O)=C1)(NCCN(C)C)=O
MDL No. :MFCD06357404

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Application In Synthesis of [ 790263-62-6 ]

* 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 [ 790263-62-6 ]

[ 790263-62-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 97-08-5 ]
  • [ 108-00-9 ]
  • [ 790263-62-6 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 0 - 25℃; for 3h;Inert atmosphere; Synthesis of 4-chloro-N-(2-(dimethylamino)ethyl)-3-nitrobenzenesulfonamide Into a 250-mL round-bottom flask under a nitrogen atmosphere, was placed a solution of (2- aminoethyl)dimethylamine (2 g, 22.69 mmol, 1 equiv) and triethylamine (4.6 g, 45.38 mmol,2.00 equiv) in anhydrous DCM (100 ml_). Then 4-chloro-3-nitrobenzene-1 -sulfonyl chloride (6.4 g, 24.96 mmol, 1 .10 equiv) was added at 0. The resulting solution was stirred for 3 hours at 25. The reaction was then quenched by the addition of 50 ml. of water/ice. The resulting solution was extracted with DCM (3 x50 ml_), dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by a silica gel column eluting with dichloromethane/methanol (10:1 ). This resulted in 4-chloro-N-[2-(dimethylamino)ethyl]-3-nitrobenzene-1 -sulfonamide.
With triethylamine; In tetrahydrofuran; at -40 - 20℃; for 1h; General procedure: A solution containing the appropriate aliphatic or cyclic amine substituent (1 equiv.) and triethylamine (2 equiv.) in THF was added dropwise to a solution containing 4-chloro-3-nitrobenzene-l-sulfonyl chloride 5 (1 equiv.) in TH F that was cooled down to -40C. After the addition was complete, the resulting mixture was allowed to warm up to room temperature over the course of one hour. Subsequently the reaction mixture was diluted with EtOAc and washed three times with water. The organic layer was dried using anhydrous sodium sulphate before being concentrated in vacuo. The crude reaction products 6-12 were used without any further purification.
 

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