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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23658생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/23658

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574363—
반응물1-(2,6-Dimethoxyphenyl)-2-(methylamino)ethan-1-olHCID 22574395—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(4-chlorobenzyl)-2-{[[2-(2,6-dimethoxyphenyl)-2-hydroxyethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 2257440652.6%

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온도60 °C

반응 단계

A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (50 mg, 0.13 mmol), 1-(2,6-dimethoxyphenyl)-2-(methylamino)ethanol (PNU-149291, Arch. Intern. Pharmacodyn. 1965, 154, 26-39) (42 mg, 0.20 mmol) and diisopropylethylamine (34 μL, 0.20 mmol) in dry DMF (2.7 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 7 hours at that temperature. After cooling to room temperature, the solution was diluted with water (7 mL). The resulting milky suspension was stirred vigorously for 30 minutes, and then left standing overnight at room temp. The mixture was filtered, and the collected solid was washed with water and dried in vacuo, leaving a white solid. Recrystallization from acetonitrile (10 mL, dissolved with warming and then cooled to 0° C. overnight) gave the title compound (39 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-797449f7fa6946f490124dbc304acff7
출처 메모uspto-grants-2005_02