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ChemicalBook CAS DataBase List 3-Bromo-6-chloro-1H-indazole
885521-34-6

3-Bromo-6-chloro-1H-indazole synthesis

2synthesis methods
6-Chloro-1H-indazole

698-25-9

3-Bromo-6-chloro-1H-indazole

885521-34-6

Step 1a. 6-Chloro-1H-indazole (3.0 g, 19.66 mmol) was suspended in 2 M NaOH solution (70 mL) and a solution of bromine (2.32 g, 14.52 mmol) in 2 M NaOH (30 mL) was added slowly and dropwise. The reaction mixture was stirred at room temperature for 1.5 hours. Upon completion of the reaction, the pH was adjusted to 8 with 3 M HCl, followed by liquid-liquid partitioning with ethyl acetate and brine. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether) to afford the target compound 3-bromo-6-chloro-1H-indazole as a yellow solid (3.4 g, 44% yield).ESI-MS m/z = 231.00, 233.00 [M + H]+.

61072-56-8 Synthesis
4-CHLORO-2-FLUOROBENZALDEHYDE

61072-56-8
291 suppliers
$14.00/5g

-

Yield:-

Steps:

Multi-step reaction with 2 steps
1: hydrazine hydrate; dmap; pyridine / 100 °C
2: sodium hydroxide; bromine / water / 20 °C

References:

THE REGENTS OF THE UNIVERSITY OF CALIFORNIA;HOGENKAMP, Derk WO2013/169907, 2013, A1

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