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HRID 526153作成日:2026年10月26日

6-Methoxy-3-pyridinylamine → HCID 178471946、化合物

https://huagongshe.com/reaction/526153

反応式

関与物質

役割名称HCID仕込み量
反応物6-Methoxy-3-pyridinylamineHCID 81121—
反応物Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl esterHCID 97734—
溶媒ChlorobenzeneHCID 7964—
生成物HCID 178471946HCID 17847194684.1%

反応条件

温度135 °C

反応手順

A mixture of ethyl 2-(ethoxymethylene)-3-oxobutanoate (100 g, 0.54 mol) and 2-methoxy-5-aminopyridine (67 g, 0.54 mol) in chlorobenzene (500 mL) was heated at 135° C. for 4 h in a round bottomed flask that was equipped with a distillation apparatus to collect the ethanol generated during the reaction. The reaction mixture was cooled and concentrated and the residue was triturated in diethylether and filtered to obtain the desired product (120 g, 84%) as an off-white solid: 1H NMR (500 MHz, CDCl3) δ 12.74 (d, 12.3 Hz, 1H), 8.35 (d, J=13.0 Hz, 1H), 8.07 (d, J=2.8 Hz, 1H), 7.55 (d, J=8.8, 2.9 Hz, 1H), 6.79 (d, J=8.8 Hz, 1H), 4.30 (q, J=7.1 Hz, 2H), 2.55 (s, 3H), 1.33 (t, J=7.1 Hz, 1H); ESI MS m/z 265 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09345709B2
出典データセットuspto-grants-2016_05
ORD IDord-dd98bd0e315e41bbbf0477496d67e4b3
出典メモuspto-grants-2016_05