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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23685생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/23685

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Rac-2-(methylamino)-1-quinolin-2-ylethanolHCID 10149073—
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-quinolin-2-ylethyl)(methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 1031197559.1%

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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 (150 mg, 0.38 mmol), 2-(methylamino)-1-quinolin-2-ylethanol (Preparation 63)(150 mg, 0.74 mmol) and diisopropylethylamine (134 μL, 0.76 mmol) in dry DMF (5 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 6 hours at that temperature. After cooling to room temperature, the solution was diluted with water (15 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 (126 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-29b8a304daac46fbae77ea798b577f56
출처 메모uspto-grants-2005_02