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HRID 2217964作成日:2026年10月27日

Ethyl 5-aminopyridazine-4-carboxylate → 5-[2-(2,4,6-Trifluorophenyl)-acetylamino]-pyridazine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2217964

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 5-aminopyridazine-4-carboxylateHCID 12352298—
反応物2,4,6-Trifluorophenylacetyl chlorideHCID 57428015—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TolueneHCID 1140—
生成物5-[2-(2,4,6-Trifluorophenyl)-acetylamino]-pyridazine-4-carboxylic acid ethyl esterHCID 68939424101.7%

反応条件

温度70 °C

反応手順

5-Aminopyridazine-4-carboxylic acid ethyl ester (1.26 g, prepared according to J. Het. Chem., (1968), 5, 845) was dissolved in dry toluene (125 ml) at 90° C., and DMAP (0.92 g) was added. 2,4,6-Trifluorophenylacetyl chloride (1.75 g of 95% purity material) was added dropwise with stirring at 70° C., and a white solid precipitated. The reaction was stirred at reflux for 5 hours and then filtered hot. The filtrate was evaporated to give 5-[2-(2,4,6-trifluorophenyl)-acetylamino]-pyridazine-4-carboxylic acid ethyl ester as a white solid (2.6 g), m.p. 143-144° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07410967B2
出典データセットuspto-grants-2008_08
ORD IDord-00ec7cec4a364349b01b9e1274154ad2
出典メモuspto-grants-2008_08