戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2056611作成日:2026年10月27日

Sodium Cyanide → 6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid (PYRIDIN-2-YL-METHYL)AMIDE

https://huagongshe.com/reaction/2056611

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CyanideHCID 8929—
反応物2-Pyridinamine, N-methyl-HCID 20727—
反応物6-[4-(2-Trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid methyl esterHCID 66849526—
生成物6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid (PYRIDIN-2-YL-METHYL)AMIDEHCID 1603609548%

反応手順

A mixture of 6-[4-(2-Trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid methyl ester (0.099 g, 0.25 mmol), pyridin-2-yl-methylamine (0.7 mL) and sodium cyanide (0.245 g, 0.5 mmol) was stirred at ambient temperature overnight and purified by column chromatography to yield the title compound in 48% yield (0.057 g). m.p. 179-181° C. 1H NMR (300 MHz, CDCl3) δ 8.81, 8.59, 8.12, 7.78-7.50, 7.37, 7.21-7.13, 6.93, 4.83, 4.17-3.66, 3.37. 13C NMR (75 MHz, CDCl3) δ 167.6, 163.3, 160.0, 156.5, 149.0, 145.3, 137.0, 134.2, 132.4, 129.5, 127.2, 122.5, 121.9, 112.3, 46.4, 44.6, 44.4, 41.3. MS (ES+) m/z 471 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07335658B2
出典データセットuspto-grants-2008_02
ORD IDord-573499f9cab24bd8b626bb4deb4811ae
出典メモuspto-grants-2008_02