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HRID 15741作成日:2026年10月23日

Dimethylformamide dimethyl acetal → Ethyl 1-(4-chlorophenylsulfonyl)-3-((dimethylamino)methylene)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate

https://huagongshe.com/ja/reaction/15741

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物Ethyl 1-(4-chlorophenylsulfonyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylateHCID 59342383—
生成物Ethyl 1-(4-chlorophenylsulfonyl)-3-((dimethylamino)methylene)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylateHCID 68502343—

反応条件

温度100 °C

反応手順

Compound 103 (5.0 g, 15 mmol) was dissolved in DMF-DMA (20 mL) and heated at 100° C. for 30 minutes. The reaction mixture was concentrated in vacuo to yield compound 104 as a yellow oil that was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732609B2
出典データセットuspto-grants-2010_06
ORD IDord-916c1a439c9a48dfb8e5e3b3454c7fcd
出典メモuspto-grants-2010_06