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Chemical Structure| 152879-73-7 Chemical Structure| 152879-73-7

Structure of 152879-73-7

Chemical Structure| 152879-73-7

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Product Details of [ 152879-73-7 ]

CAS No. :152879-73-7
Formula : C9H9NO2S
M.W : 195.24
SMILES Code : O=S(C1=CC2=C(NC=C2)C=C1)(C)=O
MDL No. :MFCD13190320

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Application In Synthesis of [ 152879-73-7 ]

* 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 [ 152879-73-7 ]

[ 152879-73-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 387350-92-7 ]
  • [ 152879-73-7 ]
YieldReaction ConditionsOperation in experiment
100% With manganese(IV) oxide; In dichloromethane; at 20℃; Example 112; 2-(3-Fluoro-phenyl)-pyrimidine-5-carboxylic acid (5-methanesulfonyl-indol-l-yl)-amide; Step 1 : A solution of 5-methanesulfonyl-indoline (4.11 mmol) and MnO2 (20.55 mmol) in DCM (20 mL) is stirred at rt overnight. The reaction mixture is filtered and the filtrate is concentrated in vacuo to afford 5 -methanesulfonyl- 1 H-indole (782 mg, 100%) as a solid. MS: 196 (M+H); 1H NMR (300 MHz, CDCl3): δ 3.09 (s, 3H), 6.71 (s, H), 7.39 (s, H), 7.53 (d, H), 7.74 (m, H), 8.30 (s, H), 8.66 (br, N-H).
71% With manganese(IV) oxide; In chloroform; at 20℃; for 9h; (a) Step 1 A solution of <strong>[387350-92-7]5-(methylsulfonyl)indoline</strong> (0.213 g, 1.08 mmol) in chloroform (4 mL) was added with manganese dioxide (0.939 g, 10.8 mmol), and the mixture was stirred at room temperature for 9 hours. The reaction mixture was filtered through Celite, and the resulting filtrate was concentrated to obtain 5-(methylsulfonyl)-1H-indole (0.151 g, 71%). 1H NMR (300 MHz, DMSO-d6) δ 3.08 (s, 3H), 6.71 (t, J = 2.2 Hz, 1H), 7.38 (t, J = 2.9 Hz, 1H), 7.53 (d, J = 8.8 Hz, 1H), 7.72-7.75 (m, 1H), 8.30 (br s, 1H), 8.57 (br s, 1H).
 

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