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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1068009생성일: 2026년 10월 25일

Synephrine → N-[(4-chlorophenyl)methyl]-6-[[[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-methyl-amino]methyl]-1-methyl-4-oxo-quinoline-3-carboxamide

https://huagongshe.com/reaction/1068009

반응식

참여 물질

역할이름HCID투입량
반응물SynephrineHCID 7172—
반응물DiisopropylethylamineHCID 81531—
반응물N-(4-Chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamideHCID 21192571—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-[(4-chlorophenyl)methyl]-6-[[[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-methyl-amino]methyl]-1-methyl-4-oxo-quinoline-3-carboxamideHCID 984906874.2%

반응 단계

A solution of N-(4-chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide (0.09 gm) from Preparation No. 35 in dry DMF (2 mL) containing diisopropylethylamine (0.07 mL) is treated with synephrine (0.05 gm). The reaction mixture is stirred overnight. The reaction mixture is diluted with dichloromethane (50 mL) and washed with water (2×10 mL), brine (10 mL), dried (Na2SO4) and concentrated under reduced pressure. The residue is purified by flash column chromatography eluting with 3% to 6% methanol in dichloromethane and then by recrystallization from toluene to afford 0.09 gm of the title compound as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06248739B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-5a0bd78eeaa84841a4c8b0f8c058ad95
출처 메모uspto-grants-2001_06