戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 64459作成日:2026年10月24日

Cyclopentanemethanol → N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-(cyclopentylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/ja/reaction/64459

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentanemethanolHCID 77195—
反応物CyanomethylenetributylphosphoraneHCID 4622928—
反応物N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamideHCID 86713409—
溶媒TolueneHCID 1140—
生成物N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-(cyclopentylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamideHCID 86713474—

反応条件

温度110 °C

反応手順

A mixture of 120 mg of N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamide, 60 μl of cyclopentylmethanol, 156 μl of (tributylphosphoranylidene)acetonitrile, and 2.4 ml of toluene was stirred at 110° C. for 16 hours, followed by purification using silica gel chromatography, to obtain 100 mg of N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-(cyclopentylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447090B2
出典データセットuspto-grants-2016_09
ORD IDord-5ab65197b73f4c0aac187c473560d72d
出典メモuspto-grants-2016_09