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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1068006Erstellt: 25. Oktober 2026

N-Methylphenylethanolamine → N-(4-Chlorobenzyl)-6-{[(2-hydroxy-2-phenylethyl)(methyl)-amino]methyl}-1-methyl-4-oxo-1,4-dihydro-3quinolinecarboxamide

https://huagongshe.com/reaction/1068006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylphenylethanolamineHCID 913—
EduktDiisopropylethylamineHCID 81531—
EduktN-(4-Chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamideHCID 21192571—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktN-(4-Chlorobenzyl)-6-{[(2-hydroxy-2-phenylethyl)(methyl)-amino]methyl}-1-methyl-4-oxo-1,4-dihydro-3quinolinecarboxamideHCID 2119253163,8%

Reaktionsschritte

A solution of N-(4-chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide (0.06 gm) from Preparation No. 35 in dry NMP (2 mL) containing diisopropylethylarnine (0.04 mL) is treated with α-(methylaminomethyl)-benzyl alcohol (0.04 gm). The reaction mixture is shaken at room temperature for 3 days then concentrated under reduced pressure. The residue is partioned between dichloromethane and water. The separated organic layer is washed with two additional portions of water, brine, dried (Na2SO4) and concentrated under reduced pressure. The residue is adsorbed onto silica and purified by flash column chromatography eluting with 2% to 6% methanol in dichloromethane and then by recrystallization from ethyl acetate-hexanes to afford 0.05 gm of the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06248739B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-69358d5342f5415e8d81080eb6212e47
Quellennotizuspto-grants-2001_06