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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1068009Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSynephrineHCID 7172—
EduktDiisopropylethylamineHCID 81531—
EduktN-(4-Chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamideHCID 21192571—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[(4-chlorophenyl)methyl]-6-[[[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-methyl-amino]methyl]-1-methyl-4-oxo-quinoline-3-carboxamideHCID 984906874,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06248739B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-5a0bd78eeaa84841a4c8b0f8c058ad95
Quellennotizuspto-grants-2001_06