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CAS No. : | 7254-19-5 | MDL No. : | MFCD00022705 |
Formula : | C9H6BrNO2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | YAULOOYNCJDPPU-UHFFFAOYSA-N |
M.W : | 240.05 | Pubchem ID : | 252137 |
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 |
---|---|---|
2% | With N-ethyl-N,N-diisopropylamine; HATU; In 1-methyl-pyrrolidin-2-one; at 20℃; for 48h; | To a mixture of 5-bromo-1H-indole-2-carboxylic acid (264 mg, 1.10 mmol, 1.0 eq.) and HATU (500 mg, 1.32 mmol, 1.2 eq.) in NMP (30 mL) were added<strong>[20358-03-6]5-bromo-1,3-benzothiazol-2-amine</strong> (250 mg, 1.10 mmol, 1.0 eq.) andDIPEA (0.38 mL, 2.18 mmol, 2.0 eq.).The reaction mixture was stirred at room temperature during 48 hours, then quenched with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4, the solvent evaporated under reduced pressure and the residue purified by silica gel flash-column chromatography (eluent: heptane/EtOAc, 90/10 to 70/30) to afford26das a pale green solid (8 mg, 2 percent).1H NMR(DMSO-d6, 400 MHz):d(ppm): 7.39 (1H, dd, J6-7= 8.8Hz, J6-4=1.4Hz, H6), 7.45 (1H, d, J7-6= 8.8Hz, H7), 7.29 (1H, t, J5-4=J5-6=7.6Hz, H5), 7.51 (1H, dd, J6?-7?= 8.8Hz, J6?-4?= 1.4Hz, H6?), 7.72 (1H, s, H3), 7.95 (1H, s, H4), 7.99 (1H, s, H4?), 8.01 (1H, d, J7?-6?= 8.8Hz, H7?), 12.21 (1H, s, indolic H), 13.17 (1H, s, amide H).13C NMR (DMSO-d6, 100 MHz):d(ppm): 106.5 (C3), 113.2 (C5), 115.1, 119.4 (C5?), 124.1 (C7?), 124.9, 126.7 (C6?), 127.9, 129.1 (C3a), 136.6 (C7a).HRMS calcd for C16H879Br81BrN3OS: m/z = 449.8734, found: 449.8657. |
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