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HRID 1582956作成日:2026年10月25日

Sodium hydride → ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoate

https://huagongshe.com/reaction/1582956

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物3-(3-Chlorobenzoyl)-2-ethylamino-6-methylpyridineHCID 11054902—
反応物Monoethyl chloroglutarateHCID 22716689—
溶媒DimethylformamideHCID 6228—
生成物ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoateHCID 22716702—

反応手順

A DMF solution of 3-(3-chlorobenzoyl)-2-ethylamino-6-methylpyridine was treated with 60% sodium hydride and then reacted with monoethyl chloroglutarate under heating. Thereafter, the whole was worked up and purified in a usual manner to obtain ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoate. The resulting compound was reacted with sodium methoxide in ethanol under heating, then concentrated sulfuric acid was added to the reaction mixture, followed by reaction under heating for 2 days. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain ethyl 3-[4-(3-chlorophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]propanoate. MS: 399.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06740662B1
出典データセットuspto-grants-2004_05
ORD IDord-275262b710cf4a448b90a8a6fff1385a
出典メモuspto-grants-2004_05