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CAS No. : | 942947-95-7 | MDL No. : | MFCD11110693 |
Formula : | C5H3BrClN3O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | BLGCPXIDEMLKMS-UHFFFAOYSA-N |
M.W : | 252.45 | Pubchem ID : | 45480236 |
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 |
---|---|---|
99% | With N-Bromosuccinimide In acetonitrile at 80℃; | A solution of 4-chloro-3-nitropyridin-2-amine (2 g, 11.5 mmol) and N-bromosuccinimide (2.5 g, 13.8 mmol) in ACN (125 mL) was heated at 80 °C. After 1h, the reaction mixture was cooled was cooled to room temperature and volatiles were removed under reduced pressure. Purification (FCC, SiO2, 0-5percent EtOAc in DCM), afforded the title compound (2.9 g, 99percent). MS (ESI): mass calcd. for C5H3BrClN3O2, 250.9; m/z found, 251.8 [M+H]+.1H NMR (400 MHz, DMSO-d6) δ 8.42 (s, 1H), 7.37 (br s, 2H). |
85% | With N-Bromosuccinimide In acetonitrile at 80℃; for 1 h; | 4-Chloro-3-nitropyridin-2-amine (0.1 0 g, 0.58 mmol) was dissolved in dryacetonitrile (20 ml). To the stirred solution was then added N-bromosuccinimide (0.124g, 0.70 mmol), and the reaction mixture was heated at 80 °C for 1 h. Volatiles wereremoved in vacuo and the residue purified by silica column chromatography (elution with25 dichloromethane) to provide the title compound as a pale brown powder (0.125 g, 85percent).1 H-NMR (500 MHz, DMSO-d6) 7.35 (s, 2H, NH2), 8.41 (s, 1 H, 6-H). |
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