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Chemical Structure| 17459-03-9 Chemical Structure| 17459-03-9

Structure of 17459-03-9

Chemical Structure| 17459-03-9

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Product Details of [ 17459-03-9 ]

CAS No. :17459-03-9
Formula : C8H10N2O4S
M.W : 230.24
SMILES Code : O=S(C1=CC=C([N+]([O-])=O)C=C1)(N(C)C)=O
MDL No. :MFCD00277215
InChI Key :ZCWXRMBVAKOURU-UHFFFAOYSA-N
Pubchem ID :2747580

Safety of [ 17459-03-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 17459-03-9 ]

* 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 [ 17459-03-9 ]

[ 17459-03-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17459-03-9 ]
  • [ 1709-59-7 ]
YieldReaction ConditionsOperation in experiment
95% With hydrogen;palladium on carbon; In methanol; Step 2. Under H2, N,N-dimethyl-4-nitrobenzenesulfonamide (879 mg, 3.8 mmol, 1.0 equiv.) was catalytically hydrogenated in the presence of Pd/C (40 mg) in MeOH (25 mL.). When no more H2 was consumed, the reaction mixture was filtered. The filtrate was concentrated and crystallized to afford compound 4-amino-N,N-dimethyl benzenesulfonamide (722 mg, 95%).
palladium; In methanol; b. 4-(N,N-dimethyl)sulfamoylaniline. A solution of N,N-dimethyl-4-nitrobenzene sulfonamide (1.00 g) in methanol (100 mL) was treated with 10% (w/v) palladium on carbon (200 mg). The mixture was placed under a hydrogen atmosphere (3 atm) and agitated for 6 h. The mixture was filtered through diatomaceous earth and the filtrate was concentrated. The crude product was triturated with hexane/ether (20 mL, 9/1 (v/v)) to afford the title compound as an off white powder. 1H NMR (300 MHz, DMSO-d6): delta7.36 (d, J=8.7 Hz, 2H), 6.65 (d, J=8.7 Hz, 2H), 6.05 (s, 2H), 2.51 (s, 6H).
B. 4-(N,N-Dimethylaminosulfonyl)aniline Using methods substantially equivalent to those described in Example 173-B, 4-(N,N-dimethylaminosulfonyl)-aniline (11.7 g, 85%) was prepared from 4-(N,N-dimethylaminosulfonyl)nitrobenzene 1H-NMR; IS-MS, m/e 201.2 (m+1); Analysis for C8H12N2O2S: Calcd: C, 47.98; H, 6.04; N, 13.99; Found: C, 48.30; H, 6.03; N, 13.74.
 

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