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ChemicalBook CAS DataBase List 5-BROMO-7-NITRO-1H-INDAZOLE
316810-82-9

5-BROMO-7-NITRO-1H-INDAZOLE synthesis

2synthesis methods
77811-44-0 Synthesis
4-Bromo-2-methyl-6-nitroaniline

77811-44-0
248 suppliers
$6.00/1g

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Yield:316810-82-9 47.7%

Reaction Conditions:

with acetic acid;sodium nitrite in water at 0 - 20; for 6 h;

Steps:

9
Starting material 20a (1.00 g, 4.32 mmol) was dissolved in 15 mL of AcOH.An aqueous solution (2 mL) of sodium nitrite (0.66 mg, 9.52 mmol) was added at 0 °C.After the addition, rt was stirred for 6 hours.The TLC monitors the reaction of the starting material completely, spins the reaction solution, extracts, and the crude product is purified by column chromatography.An orange powder compound 20b (0.5 mg, 2.07 mmol) was obtained in a yield: 47.7%.

References:

Xihua University;Yang Lingling;Qian Shan;Li Guobo;Chen Feng;Li Chao;He Yanying;Wang Zhouyu;Lai Peng CN108689937, 2018, A Location in patent:Paragraph 0179; 0181; 0182

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