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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 反応物 | Ethyl 1-(4-chlorophenylsulfonyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate | HCID 59342383 | — |
| 生成物 | Ethyl 1-(4-chlorophenylsulfonyl)-3-((dimethylamino)methylene)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate | HCID 68502343 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07732609B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-916c1a439c9a48dfb8e5e3b3454c7fcd |
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| 出典メモ | uspto-grants-2010_06 |
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