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HRID 406455作成日:2026年10月26日

Halauxifen-methyl → Methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/406455

反応式

関与物質

役割名称HCID仕込み量
反応物Halauxifen-methylHCID 16656802—
反応物4-Chloro-2-fluoro-3-methoxyphenylboronic acidHCID 44129706—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物Methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylateHCID 67210962—

反応手順

Another embodiment of the present disclosure includes a method of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate. The method comprises producing an aqueous solution comprising 4-chloro-2-fluoro-3-methoxyphenylboronic acid. Methyl isobutyl ketone is added to the aqueous solution. The methyl isobutyl ketone and 4-chloro-2-fluoro-3-methoxyphenylboronic acid are separated from the water. The 4-chloro-2-fluoro-3-methoxyphenylboronic acid is reacted with methyl 4-(acetylamino)-3,6-dichloropyridine-2-carboxylate in methyl isobutyl ketone to produce methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate, which is deacetylated to produce methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754110B2
出典データセットuspto-grants-2014_06
ORD IDord-6a0a6ab1bfdf4f6cba770428f121eed8
出典メモuspto-grants-2014_06