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HRID 840528作成日:2026年10月26日

Methyl iodide → HCID 22610929、化合物

https://huagongshe.com/reaction/840528

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 3-amino-4,4,4-trifluoro-2-butenoateHCID 136209—
反応物2-Ethoxycarbonylamino-3-fluoro-5-chloropyridineHCID 22610930—
反応物HCID 178418361HCID 178418361—
溶媒1-MethylpyrrolidineHCID 8454—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 22610929HCID 22610929—

反応手順

Under a nitrogen atmosphere, while cooling and stirring, a solution of 22.7 g 4,4,4-trifluoro-3-amino-2-butenoic acid ethyl ester is added dropwise to 5.1 g of a sodium hydride dispersion (60%) in 60 ml N-methylpyrrolidine at 0-5° C. and stirred at 22° C. until hydrogen evolution is complete. Then 23.7 g 2-ethoxicarbonylamino-3-fluoro-5-chloropyridine (Example H1) is added and the reaction mixture heated for about 5 hours to 120° C. The mixture is then cooled, 16.7 g methyl iodide is added dropwise and stirring is continued overnight at 22° C. After the reaction mixture has been taken up in ethyl acetate, it is washed with ice water, dried over sodium sulfate, filtered, and concentrated by evaporation. The residue obtained is recrystallized from ethyl acetate/n-hexane. The title compound is obtained with a melting point of 133-134° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06369002B1
出典データセットuspto-grants-2002_04
ORD IDord-3dfbdfd7f56740fe8ffc76e0afe2a60c
出典メモuspto-grants-2002_04