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HRID 1502352作成日:2026年10月25日

5-Bromo-4,6-dimethylpyridin-3-amine → 4-bromo-5-methyl-1H-pyrazolo[3,4-c]pyridine

https://huagongshe.com/reaction/1502352

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-4,6-dimethylpyridin-3-amineHCID 7060666—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
生成物4-bromo-5-methyl-1H-pyrazolo[3,4-c]pyridineHCID 6797640153%

反応条件

温度60 °C

反応手順

To a solution of 5-bromo-4,6-dimethylpyridin-3-amine (1.00 g, 4.98 mmol) in acetic acid (12 mL) at ambient temperature was added sodium nitrite (364 mg, 5.28 mmol) and the mixture heated to 60° C. for 1.5 hr. The cooled reaction mixture was concentrated in vacuo, the residue partitioned between ethyl acetate and saturated aqueous sodium bicarbonate and the biphasic mixture filtered through a celite pad. The separated aqueous phase was extracted with ethyl acetate, and the combined organic phases washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica, ISCO, 10-100% ethyl acetate in heptane) to afford the title compound as a pale brown solid (554 mg, 53%). 1H NMR (300 MHz, DMSO) δ 13.91 (s, 1H), 8.95 (s, 1H), 8.14 (s, 1H), 2.67 (s, 3H). LCMS: M+H+=212 & 214.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09206175B2
出典データセットuspto-grants-2015_12
ORD IDord-b862ed3e55e84604b5e6a22148427850
出典メモuspto-grants-2015_12