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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721091Erstellt: 24. Oktober 2026

p,alpha-DIMETHYLBENZYL ALCOHOL → 1-(4-Methylphenyl)ethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate

https://huagongshe.com/de/reaction/721091

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp,alpha-DIMETHYLBENZYL ALCOHOLHCID 10817—
EduktTriphosgeneHCID 94429—
Edukt4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylanilineHCID 21890421—
EduktToluene triethylamineHCID 22504574—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(4-Methylphenyl)ethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamateHCID 2189003673,3%

Reaktionsschritte

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline (80 mg) was added to toluene/triethylamine=10/1 (8 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (111 mg) in methylene chloride was then added to the solution, and the mixture was heated under reflux for 15 min. Subsequently, 4-methyl-α-methylbenzyl alcohol (50 mg) was added thereto, and the mixture was further stirred with heating under reflux for 2 hr. After the completion of the reaction, the reaction solution was allowed to cool to room temperature before distilled water was added thereto. The mixture was subjected to separatory extraction with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution and saturated brine. The washed solution was dried over sodium sulfate and was concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (88mg, yield 68%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-f4d8cc99eb694ad49393c5bc975c7366
Quellennotizuspto-grants-2006_11