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HRID 221866作成日:2026年10月26日

Acetic Acid → 5-tert-butyl-2-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine hydrochloride

https://huagongshe.com/reaction/221866

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
反応物3-Methoxyphenylhydrazine hydrochlorideHCID 2723940—
溶媒EthanolHCID 702—
生成物5-tert-butyl-2-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine hydrochlorideHCID 6702227456%

反応手順

To a solution of 4,4-dimethyl-3-oxo-pentanenitrile (5.0 g, 40 mmol) and 3-methoxy-phenylhydrazine hydrochloride (7.0 g, 40 mmol) in anhydrous ethanol (200 mL) was added acetic acid (1.2 mL). The reaction mixture was heated at reflux overnight, then cooled to room temperature and concentrated at reduced pressure. The residue was combined with ethyl acetate (200 mL), and washed with saturated aq NaHCO3, water, and brine. The solution was dried over Na2SO4, evaporated at reduced pressure and the solid residue was re-dissolved in ethanol (100 mL). A solution of 2M HCl in ether was added and the mixture was stirred for 30 min. The solvent was removed at reduced pressure, the solid residue was triturated and washed with hexane (50 mL) and then dried in a vacuum oven overnight to give the product 5-tert-butyl-2-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine hydrochloride (5.46 g, 56%) as an off-white solid. 1H-NMR (DMSO-d6) δ 7.50 (t, 1H), 7.10 (m, 3H), 5.60 (s, 1H), 3.80 (s, 3H), 1.30 (s, 9H); MS LC-MS [M+H]+=246.2, RT=1.90 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207166B2
出典データセットuspto-grants-2012_06
ORD IDord-51567a5ef0f44559aad74e4541740fbb
出典メモuspto-grants-2012_06