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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23627생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/23627

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-(Methylamino)-1-(1-oxidopyridin-3-yl)ethanolHCID 22574315—
반응물N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574363—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(4-chlorobenzyl)-2-{[[2-hydroxy-2-(1-oxidopyridin-3-yl)ethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 2257431659.4%

반응 단계

A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (135 mg, 0.342 mmol), 2-(methylamino)-1-(1-oxidopyridin-3-yl)ethanol (Preparation 86, 69 mg, 0.50 mmol) and diisopropylethylamine (89 μL, 0.51 mmol) in dry DMF (5.0 mL) was stirred for 20 hours at room temperature. The solution was then diluted with water (20 mL). The resulting precipitate was collected by filtration and the collected solid was dried in vacuo, providing 107 mg of the titled compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-45faeedd0f14429585b25d393e3512f8
출처 메모uspto-grants-2005_02