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HRID 75588作成日:2026年10月24日

Pentane → 3-(tert-Butyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-amine

https://huagongshe.com/ja/reaction/75588

反応式

関与物質

役割名称HCID仕込み量
反応物PentaneHCID 8003—
反応物(4-Methoxyphenyl)hydrazineHCID 77023—
反応物Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
生成物3-(tert-Butyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-amineHCID 1113939582.5%

反応手順

4,4-Dimethyl-3-oxo-pentanenitrile (14.28 g, 114 mmol) and 4-methoxyphenyl hydrazine (19.89 g, 114 mmol) were dissolved in a mixture of absolute ethanol (170 mL) and glacial acetic acid (5.0 mL) then heated to reflux for 3 h, before allowing to standing overnight at RT. The resulting red/brown solid was filtered off, and the filtrate was then diluted with water (500 mL), and basified with 880 ammonia solution until the pH=5. This aqueous solution was extracted into diethyl ether (3×). The combined organics were dried (MgSO4) and evaporated in vacuo to a brown oil. Trituration (pentane) gave the title compound as a light purple/brown solid (23.07 g, 94.1 mmol, 82%). LCMS (method 1): Rt 2.87 min, m/z 246/247 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835431B2
出典データセットuspto-grants-2014_09
ORD IDord-9677a2f941934c0ca1ef9a121bd37711
出典メモuspto-grants-2014_09