化工社化工社 化学情報印刷レポート · 研究参考用
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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Halauxifen-methyl | HCID 16656802 | — |
| 反応物 | 4-Chloro-2-fluoro-3-methoxyphenylboronic acid | HCID 44129706 | — |
| 溶媒 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 生成物 | Methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08754110B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-6a0a6ab1bfdf4f6cba770428f121eed8 |
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| 出典メモ | uspto-grants-2014_06 |
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