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HRID 23629作成日:2026年10月24日

Diisopropylethylamine → N-(4-chlorobenzyl)-2-{[[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-hydroxyethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide

https://huagongshe.com/ja/reaction/23629

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2-(methylamino)ethan-1-olHCID 22574300—
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-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-hydroxyethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 1028980773.1%

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 (100 mg, 0.253 mmol), 1-(1,4-benzodioxan-6-yl)-2-(methylamino)ethanol (Preparation 13, 79 mg, 0.38 mmol), and diisopropylethylamine (66 μL, 0.38 mmol) in dry DMF (5.5 mL) was stirred at room temperature 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 (105 mg) as an off 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-1150ca91e56143a0a81167459b8a350f
出典メモuspto-grants-2005_02