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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

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrahydrothiopyran-4-oneHCID 66173—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamideHCID 21906309—
溶媒TetrahydrofuranHCID 8028—
溶媒Acetic acid methanolHCID 10129899—
生成物5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamideHCID 2190656140.1%

反応条件

温度50 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06635657B1
出典データセットuspto-grants-2003_10
ORD IDord-bd380b5f06b94f91aac911c648f35ed9
出典メモuspto-grants-2003_10