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ChemicalBook CAS DataBase List 5-bromo-1H-pyrazolo[3,4-c]pyridine
929617-35-6

5-bromo-1H-pyrazolo[3,4-c]pyridine synthesis

3synthesis methods
156118-16-0 Synthesis
2-BROMO-5-AMINO-4-PICOLINE

156118-16-0
147 suppliers
$11.00/250mg

-

Yield:929617-35-6 59%

Reaction Conditions:

with acetic acid;sodium nitrite at 20;

Steps:

Synthesis of 5-bromo-1H-pyrazolo[3,4-c]pyridine (28)
To a solutionof 27(4.00 g, 21.4 mmol) in AcOH (300 ml) was added NaNO2 (1.48 g, 21.4mmol) and stirred overnight at roomtemperature. The reaction mixture was concentrated in vacuo. The residue was diluted with EtOAc and washed with saturatedNaHCO3 aqueous solution and brine. Theorganic layer was dried over anhydrous MgSO4 and reduced underpressure. The residue was purified bysilica gel column chromatography (0-50% EtOAc in hexanes) to afford 28 as a yellow solid (2.48 g, 59%yield).1H NMR (300 MHz, CDCl3): δ ppm7.86 - 7.90 (m, 1 H), 8.09 - 8.14 (m, 1 H), 8.83 - 8.88 (m, 1 H).MS ESI/APCI Dual m/z: 198 [M+H] .

References:

Matsuda, Daisuke;Kobashi, Yohei;Mikami, Ayako;Kawamura, Madoka;Shiozawa, Fumiyasu;Kawabe, Kenichi;Hamada, Makoto;Oda, Koji;Nishimoto, Shinichi;Kimura, Kayo;Miyoshi, Masako;Takayama, Noriko;Kakinuma, Hiroyuki;Ohtake, Norikazu [Bioorganic and Medicinal Chemistry Letters,2016,vol. 26,# 15,p. 3441 - 3446] Location in patent:supporting information

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