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HRID 1174839作成日:2026年10月25日

Water → 3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenol

https://huagongshe.com/reaction/1174839

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Pyridinium hydrochlorideHCID 21584435—
反応物5-tert-butyl-2-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine hydrochlorideHCID 67022274—
溶媒Ethyl AcetateHCID 8857—
生成物3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenolHCID 5955796619%

反応条件

温度195 °C

反応手順

In a 500 mL round bottom flask was added 5-tert-butyl-2-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine hydrochloride (8.42 g, 30 mmol) and pyridinium hydrochloride (13.8 g, 120 mmol). The reaction mixture was heated neat at 195° C. with stirring for 3 h. The mixture was cooled to room temperature, water (300 mL) and EtOAc (300 mL) were added, and then the organic phase was washed with saturated aq NaHCO3 and brine, dried (Na2SO4) and concentrated at reduced pressure. The residue was purified by MPLC (80:20 hexane/EtOAc) to give the product 3-(5-amino-3-tert-butyl-pyrazol-1-yl)-phenol (1.3 g, 19%). 1H-NMR (DMSO-d6) δ 7.20 (t, 1H), 7.00 (m, 2H), 6.50 (d, 1H), 5.30 (s, 1H), 5.10 (bs, 2H), 1.30 (s, 9H); MS LC-MS [M+H]+=232.2, RT=0.57 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07838524B2
出典データセットuspto-grants-2010_11
ORD IDord-0cd0390e4450440fbe469bf0479d133d
出典メモuspto-grants-2010_11