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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1857746Erstellt: 25. Oktober 2026

Dichloromethane → HCID 22130469, Verbindung

https://huagongshe.com/reaction/1857746

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktSodium HydroxideHCID 14798—
Edukt3-(Bromomethyl)quinolineHCID 23510331—
Edukt2-Benzyloxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1H-imidazoleHCID 178419034—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 22130469HCID 221304692,6%

Reaktionsschritte

In tetrahydrofuran (10 ml) was dissolved 245 mg (2 mmol) of 2-benzyloxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1H-imidazole (101a). To this solution, a methylene chloride solution of quinolin-3-ylmethylbromide was added at room temperature with stirring, followed by addition of 200 mg (5 mmol) of sodium hydroxide and 39 mg (0.12 mmol) of n-tetrabutylammonium bromide. After stirring for 2 hours, the mixture was left overnight and worked up. The reaction mixture was distilled off under reduced pressure. The residue was extracted with methylene chloride, and the extract was washed with water and dried. The solvent was distilled off, and the residual oil was purified by silica gel column chromatography (methylene chloride-ethyl acetate). As the first eluate, 26 g (2.6%) of 2-benzyloxymethyl-4-(3,5-dichlorophenylthio)-5-isopropyl-1-(quinolin-3-ylmethyl)-1H-imidazole (100a) was obtained. From the subsequent eluate, 730 mg of 2-benzyloxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-(quinolin-3-ylmethyl)-1H-imidazole (100b) suited to the next step of the reaction was obtained (yield 73%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06147097
Quelldatensatzuspto-grants-2000_11
ORD IDord-e9b74a75c0344ecf922f02f2085e4e1a
Quellennotizuspto-grants-2000_11