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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-Methylphenylethanolamine | HCID 913 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-(4-Chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide | HCID 21192571 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | N-(4-Chlorobenzyl)-6-{[(2-hydroxy-2-phenylethyl)(methyl)-amino]methyl}-1-methyl-4-oxo-1,4-dihydro-3quinolinecarboxamide | HCID 21192531 | 63,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06248739B1 |
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| Quelldatensatz | uspto-grants-2001_06 |
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| ORD ID | ord-69358d5342f5415e8d81080eb6212e47 |
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| Quellennotiz | uspto-grants-2001_06 |
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