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HRID 221866생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/221866

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
반응물3-Methoxyphenylhydrazine hydrochlorideHCID 2723940—
용매EthanolHCID 702—
생성물5-tert-butyl-2-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine hydrochlorideHCID 6702227456%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207166B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-51567a5ef0f44559aad74e4541740fbb
출처 메모uspto-grants-2012_06