戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 79487作成日:2026年10月25日

Benzyl Alcohol → 7-(Benzyloxy)-N-(3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/79487

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物WaterHCID 962—
反応物Potassium HydroxideHCID 14797—
反応物7-chloro-N-(3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamideHCID 67259969—
溶媒Dimethyl SulfoxideHCID 679—
生成物7-(Benzyloxy)-N-(3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamideHCID 6725964294.6%

反応条件

温度90 °C

反応手順

A mixture of 7-chloro-N-(3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide (1.0 g, 2.2 mmol; prepared as in Example 65, step C), benzyl alcohol (1.2 g, 11 mmol) and potassium hydroxide (0.61 g, 11 mmol) was dissolved in DMSO (7 mL). The reaction mixture was heated at 90° C. for 20 hours. The mixture was cooled to ambient temperature, transferred into water (100 mL) with stirring, and the resulting solid was collected by vacuum filtration and dried under vacuum to give the product (1.1 g). MS (ES+APCI) m/z=529.7 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841455B2
出典データセットuspto-grants-2014_09
ORD IDord-7a997e87398049ab9265f61df49f5c38
出典メモuspto-grants-2014_09