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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23628생성일: 2026년 10월 24일

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/ko/reaction/23628

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물alpha-[[(2-Hydroxyethyl)amino]methyl]benzyl alcoholHCID 107278—
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-hydroxyethyl)(2-hydroxy-2-phenylethyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574378—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-ff63e5480333447cb0460776cf01397d
출처 메모uspto-grants-2005_02