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HRID 535659作成日：2026年10月26日

N,N-dimethyl-7-(piperazin-1-yl)benzofuran-2-carboxamide → 7-(4-(2-(5-Acetamidopyridin-2-yl)ethyl)piperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamide

https://huagongshe.com/reaction/535659

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-dimethyl-7-(piperazin-1-yl)benzofuran-2-carboxamideHCID 59636743—
反応物N-(6-vinylpyridin-3-yl)acetamideHCID 59636765—
生成物7-(4-(2-(5-Acetamidopyridin-2-yl)ethyl)piperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamideHCID 59636773—

反応手順

The compound was prepared according to the procedure disclosed in Example 43 starting from N,N-dimethyl-7-(piperazin-1-yl)benzofuran-2-carboxamide (0.075 g, 0.27 mmol) (Example 39d) and N-(6-vinylpyridin-3-yl)acetamide (0.16 g, 0.96 mmol). The product was purified by preparative HPLC to give the title compound. Yield: 0.055 g (46%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859534B2
出典データセットuspto-grants-2014_10
ORD IDord-101f1da1c24a4e2e88cc796a61c76ab2
出典メモuspto-grants-2014_10