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HRID 550357作成日:2026年10月26日

Ethyl 2-aminopyridine-3-carboxylate → 2-[2-(2,4,6-Trifluorophenyl)-acetylamino]-nicotinic acid ethyl ester

https://huagongshe.com/reaction/550357

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-aminopyridine-3-carboxylateHCID 12433260—
反応物2,4,6-Trifluorophenylacetyl chlorideHCID 57428015—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物2-[2-(2,4,6-Trifluorophenyl)-acetylamino]-nicotinic acid ethyl esterHCID 5861723293%

反応手順

2-Aminonicotinic acid ethyl ester (2.4 g) was suspended in dry toluene (50 ml). To the stirred suspension, 2,4,6-trifluorophenylacetyl chloride (3.0 g) in dry toluene (20 ml) was added. The resulting suspension was heated to reflux for 8 hours. The reaction mixture was cooled to ambient temperature, diluted with diethyl ether (100 ml), washed with water and brine, and the organic layer was dried over magnesium sulphate. The solvent was evaporated to give 2-[2-(2,4,6-trifluorophenyl)-acetylamino]-nicotinic acid ethyl ester as a yellow solid (4.5 g, 93%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947679B2
出典データセットuspto-grants-2011_05
ORD IDord-809b9c4f66de4e5d932ec0565894e101
出典メモuspto-grants-2011_05