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CAS No. : | 78887-39-5 | MDL No. : | MFCD00236013 |
Formula : | C8H10BNO3 | Boiling Point : | - |
Linear Structure Formula : | B(OH)2C6H4NHCOCH3 | InChI Key : | IBTSWKLSEOGJGJ-UHFFFAOYSA-N |
M.W : | 178.98 | Pubchem ID : | 157274 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Ethyl 5-bromo-1-benzothiophene-2-carboxylate (2.0 g), 3-acetamidobenzene boronic acid (1.38 g), 1 M potassium carbonate aqueous solution (15 mL) and ethanol (15 mL) were added to toluene (50 mL), and stirred for 30 minutes at room temperature in an argon atmosphere. Tetrakis triphenylphosphine palladium (0.24 g) was added and refluxed for 8 hours. The mixture was extracted with ethyl acetate, the organic layer was washed with water and sodium chloride solution and dried over magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane) to obtain ethyl 5-[3-(acetylamino)phenyl]-1-benzothiophene-2-carboxylate (1.91 g) as pale brown crystals. 1H-NMR (300MHz, CDCl3) δ 1.43 (3H, t, J = 7.1 Hz), 2.22 (3H, s), 4.43 (2H, q, J = 7.1 Hz), 7.34-7.54 (3H, m), 7.69 (1H, dd, J = 1.7, 8.5 Hz), 7.85 (1H, s), 7.91 (1H, d, J = 8.5 Hz), 8.05 (1H, d, J = 1.7Hz), 8.09(1H, s) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Example 280 3-(3-Acetylamino-phenylamino)-4-methoxy-N-phenyl-benzamide The title compound has been made using the procedure of Example 154, but using <strong>[120-35-4]3-amino-4-methoxy-benzanilide</strong>, which is available from Aldrich, and 3-acetamidobenzeneboronic acid, which is available from Lancaster, as starting materials; mp 202-203 C. |
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