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HRID 491994作成日:2026年10月26日

Pentanenitrile, 4,4-dimethyl-3-oxo- → ethyl 3-(3-(3-t-butyl-5-amino-1H-pyrazol-1-yl)phenyl)propanoate

https://huagongshe.com/reaction/491994

反応式

関与物質

役割名称HCID仕込み量
反応物Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
反応物3-(3-Hydrazinophenyl)propionic acid ethyl esterHCID 58842921—
溶媒EthanolHCID 702—
生成物ethyl 3-(3-(3-t-butyl-5-amino-1H-pyrazol-1-yl)phenyl)propanoateHCID 5884289285.2%

反応手順

A mixture of Example Y (13 g, 53.3 mmol) and 4,4-dimethyl-3-oxo-pentanenitrile (6.9 g, 55 mol) in ethanol (150 mL) was heated to reflux overnight. The reaction solution was evaporated under reduced pressure. The residue was purified by column chromatography to give 3-[3-(5-amino-3-t-butyl-pyrazol-1-yl)-phenyl]-propionic acid ethyl ester (14.3 g, 45.4 mmol) as a white solid. 1H NMR (DMSO-d6): 7.39-7.32 (m, 3H), 7.11 (d, J=6.8 Hz, 1H), 5.34 (s, 1H), 5.16 (s, 2H), 4.03 (q, J=7.2 Hz, 2H), 2.88 (t, J=7.6 Hz, 2H), 2.63 (t, J=7.6 Hz, 2H), 1.19 (s, 9H), 1.15 (t, J=7.2 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531566B2
出典データセットuspto-grants-2009_05
ORD IDord-09cdeaa9159f48b4b9097837414a9823
出典メモuspto-grants-2009_05