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HRID 225883作成日:2026年10月25日

Ethyl Acrylate → Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate

https://huagongshe.com/reaction/225883

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcrylateHCID 8821—
反応物Tri-o-tolylphosphineHCID 80271—
反応物DiisopropylethylamineHCID 81531—
反応物2-Amino-5-bromo-4-methylpyridineHCID 817695—
触媒palladium(II) acetateHCID 167845—
溶媒PropionitrileHCID 7854—
生成物Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylateHCID 5744084559%

反応手順

To a stirred solution of 2-amino-5-bromo-4-methylpyridine (10 g, 54 mmole) in propionitrile (50 mL) was added ethyl acrylate (17 mL, 157 mmole), DIEA (19 mL, 106 mmole), palladium(II) acetate (0.61 g, 2.7 mmole) and tri-o-tolylphosphine (1.64 g, 5.4 mmole). The reaction was purged with argon and heated at reflux for 6 hr, then was cooled to RT and concentrated to dryness under vacuum. The resulting residue was taken up in ethyl acetate and filtered through a pad of silica gel. The filtrate was concentrated and the remaining residue was triturated with 1:1 Et2O/petroleum ether (50 mL), filtered, and dried under vacuum to give the title compound (6.50 g, 59%) as a pale yellow solid: 1H NMR (400 MHz, DMSO-d6) δ 8.31 (s, 1 H), 7.66 (d, J=16.0 Hz, 1 H), 6.40 (br s, 2 H), 6.32 (d, J=16.0 Hz, 1 H), 6.28 (s, 1 H), 4.15 (q, 2 H), 2.24 (s, 3 H), 1.24 (t, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557125B2
出典データセットuspto-grants-2009_07
ORD IDord-11ef8d546f2942e882ed85f1ac542b6a
出典メモuspto-grants-2009_07