戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 23628作成日:2026年10月24日

Diisopropylethylamine → n-(4-Chlorobenzyl)-2-{[(2-hydroxyethyl)(2-hydroxy-2-phenylethyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide

https://huagongshe.com/ja/reaction/23628

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物alpha-[[(2-Hydroxyethyl)amino]methyl]benzyl alcoholHCID 107278—
反応物N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574363—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物n-(4-Chlorobenzyl)-2-{[(2-hydroxyethyl)(2-hydroxy-2-phenylethyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574378—

反応手順

A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (75 mg, 0.190 mmol), α-2-hydroxyethylaminomethyl-benzyl alcohol (Bulletin of the Chemical Society of Japan, 56(1), 212-18; 1983)(51 mg, 0.28 mmol) and diisopropylethylamine (50 μL, 0.29 mmol) in dry DMF (4.0 mL) was heated to 60° C. for 18 hours. The solution was then diluted with water (20 mL). The resulting precipitate was collected by filtration and the collected solid was dried in vacuo at 60° C. to provide the titled compound (92 mg) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852731B2
出典データセットuspto-grants-2005_02
ORD IDord-ff63e5480333447cb0460776cf01397d
出典メモuspto-grants-2005_02