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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165920Erstellt: 25. Oktober 2026

Sodium Hydroxide → Ethyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamate

https://huagongshe.com/reaction/1165920

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt1-(4-Fluorobenzyl)-2-chlorobenzimidazoleHCID 3020241—
EduktSodium MethoxideHCID 10942334—
EduktEthyl piperidin-4-ylcarbamate hydrochlorideHCID 19861299—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamateHCID 15595031—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

19 g (0.09 mole) of ethyl 4-piperidylcarbamate hydrochloride is solubilized in 120 ml of methanol and neutralized with 17.2 ml of 5.3N sodium methylate. The mixture is filtered and the filtrate evaporated to dryness. The evaporation residue is then mixed with 21.6 g (0.083 mole) of 2-chloro-1-[(4-fluorophenyl)methyl]-1H-benzimidazole and heated to 140° C. for 5 hours. The reaction mass is taken up with methylene chloride and alkalinized with 2N sodium hydroxide. The organic phase is washed with water, dried, filtered and evaporated. The oil obtained is chromatographed on silica (eluent: methylene chloride/methanol, 97.5:2.5). Ethyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamate is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04912219
Quelldatensatzuspto-grants-1990_03
ORD IDord-571380de5f4c497b8cb3777447036cb8
Quellennotizuspto-grants-1990_03