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HRID 988679作成日:2026年10月27日
Tetrahydrothiopyran-4-one → 5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamide
https://huagongshe.com/reaction/988679
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrothiopyran-4-one | HCID 66173 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | 5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide | HCID 21906309 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Acetic acid methanol | HCID 10129899 | — |
| 生成物 | 5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamide | HCID 21906561 | 40.1% |
反応手順
5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide from Example 99-A (0.45 g, 1.25 mmol) was dissolved in 95:5 methanol-acetic acid (10 mL), followed by addition of tetrahydrothiopyran-4-one (1.46 g, 12.6 mmol) and sodium cyanoborohydride (5.0 mL of a 1 M solution in tetrahydrofuran, 6.0 mmol). After stirring at 50° C. for 96 h, the mixture was concentrated in vacuo; and the residue was directly subjected to silica gel chromatography. Elution with 9:1 dichloromethane-methanol provided 0.23 g (40%) of the title product as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06635657B1 |
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| 出典データセット | uspto-grants-2003_10 |
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| ORD ID | ord-bd380b5f06b94f91aac911c648f35ed9 |
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| 出典メモ | uspto-grants-2003_10 |
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