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Chemical Structure| 1001394-95-1 Chemical Structure| 1001394-95-1

Structure of 1001394-95-1

Chemical Structure| 1001394-95-1
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Product Details of [ 1001394-95-1 ]

CAS No. :1001394-95-1
Formula : C14H9BrFNO2S
M.W : 354.19
SMILES Code : FC1=CC2=C(C(Br)=C1)C=CN2S(=O)(C3=CC=CC=C3)=O
MDL No. :MFCD29060181

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* 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 [ 1001394-95-1 ]

[ 1001394-95-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 885520-70-7 ]
  • [ 98-09-9 ]
  • [ 1001394-95-1 ]
YieldReaction ConditionsOperation in experiment
100% With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; water; for 1h; Intermediate 36; 4-Bromo-6-fluoro-l-(phenylsulfonyl)-lH-indole; Aq. 4 M NaOH (5 mL) was added to a stirring mixture of 4-bromo-6-fluoro-lH-indole (500 mg, 2.34 mmol; Intermediate 35), benzenesulfonyl chloride (329 muL g, 2.57 mmol) and tetrabutylammonium hydrogen sulfate (78 mg, 0.23 mmol) in DCM (30 mL). The reaction mixture was stirred Ih, combined with an earlier batch of this intermediate (followed this experimental and starting with 4-bromo-6-fluoro-lH-indole, 152 mg, 0.71 mmol; Intermediate 35), washed twice with water, dried and concentrated. The product <n="93"/>(1.08 g, 100percent) was obtained as a beige solid. MS (ESI+) for Ci4H9BrFNO2S m/z 354 (M+H)+.
79% With sodium hydride; In tetrahydrofuran; mineral oil; at 20℃; for 4h;Inert atmosphere; To a solution of 4-bromo-6-fluoro-indole (2 g, 9.38 mmol) in anhydrous tetrahydrofuran (30 mL) cooled in an ice bath was added sodium hydride (0.452 g, 11.3 mmol, 60percent in mineral oil). The reaction mixture was stirred under nitrogen for 10 min before benzenesulfonyl chloride (1.44 mL, 11.3 mmol) was added. The black solution was allowed to warm to room temperature over 4 h. TLC and LCMS indicated completion of the reaction. Saturated aqueous ammonium chloride solution was added slowly, and the resulting solution was extracted with ethyl acetate (2*). The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude solid was triturated with ethanol. The resulting beige solid was collected by filtration to give 4-bromo-6-fluoro-1-(phenylsulfonyl)-1H-indole (2.6 g, 79percent yield).
 

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