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CAS No. : | 885271-63-6 | MDL No. : | MFCD03840642 |
Formula : | C9H7BrN2O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | YRCSUTRLSRFUKC-UHFFFAOYSA-N |
M.W : | 255.07 | Pubchem ID : | 24728204 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-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 |
---|---|---|
69% | With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20℃; for 1h; | Compound 2a (1.0 g, 5.68 mmol) and KOH (1.28 g, 22.7 mmol) were dissolved in DMF (15 mL) as a suspension and NBS (2.0 g, 11.4 mmol) was added.And the mixture was stirred at room temperature for 1 hour.The reaction was poured into water and extracted with EtOAc (100 mL x 2).The organic phase was washed with a saturated aqueous sodium bicarbonate solution and saturated brine, dried over sodium sulfate and filtered.The organic phase was concentrated and purified by column chromatography (EtOAc / Pet. Ether, 1/100 to 1/5, v / v).Obtained as a light yellow solid product 2b (1.0 g, 69%). |
With N-Bromosuccinimide; potassium hydroxide; In N,N-dimethyl-formamide; for 1h; | To a solution of lH-<strong>[192945-49-6]indazole-4-carboxylic acid methyl ester</strong> (380 mg, 2.2 mmol) in DMF (5 mL) was added N-bromosuccinimide (nuBS) (976 mg, 4.32 mmol) and KOeta (485 mg, 8.64 mmol). After 1 hour, the reaction mixture was diluted with saturated aqueous ammonium chloride (20 mL) and extracted with ethyl acetate (3 x 20 mL). The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine (20 mL), dried over sodium sulfate and concentrated in vacuo to afford the title compound as a solid. |
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