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HRID 1410385作成日:2026年10月27日

Sodium Acetate → 4-[5-Benzyl-3-(4-chloro-phenyl)-[1,2,4]triazol-1-yl]-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine

https://huagongshe.com/reaction/1410385

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AcetateHCID 517045—
反応物4-Hydrazinyl-6-(pyridin-2-yl)-1,3,5-triazin-2-amineHCID 608952—
反応物N-(4-chloro-thiobenzoyl)-2-phenyl-acetamideHCID 22174859—
反応物HOAc dioxaneHCID 22565020—
溶媒WaterHCID 962—
生成物4-[5-Benzyl-3-(4-chloro-phenyl)-[1,2,4]triazol-1-yl]-6-pyridin-2-yl-[1,3,5]triazin-2-ylamineHCID 2217486860%

反応条件

温度90 °C

反応手順

To a solution of N-(4-chloro-thiobenzoyl)-2-phenyl-acetamide (0.536 g, 1.85 mmol) and sodium acetate (ca. 0.25 g) in 1:1 acetic acid/1,4-dioxane (30 mL) was added 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (0.376 g, 1.85 mmol). The solution was heated to 90° C. and stirred for 15 hours. The reaction mixture was allowed to cool to room temperature, and water (100 mL) was added. The precipitate was removed by filtration, triturated with hot ethanol (300 mL), and dried to provide 0.489 g (60%) of the product as a white solid: 1H NMR (DMSO-d6) δ 8.78 (d, J=4.3 Hz, 1H), 8.32 (d, J=6.1 Hz, 2H), 8.22 (d, J=7.8 Hz, 1H), 8.06 (d, J=8.5 Hz, 2H), 7.96 (dt, J=1.5, 7.8 Hz, 1H), 7.62-7.57 (m, 3H), 7.36-7.26 (m, 2H), 7.24-7.22 (m, 2H), 7.19-7.16 (m, 1H), 4.90 (s, 2H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921547B2
出典データセットuspto-grants-2014_12
ORD IDord-78e2d5eb3c164f889f1ed70b47f636d2
出典メモuspto-grants-2014_12