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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 460536Erstellt: 26. Oktober 2026

Hydrochloric Acid → 6-[[1-Phenyl-2-propylamino-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl Ester

https://huagongshe.com/reaction/460536

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethyl iodideHCID 6328—
EduktAmmonium ChlorideHCID 25517—
EduktPropyl IsothiocyanateHCID 69403—
Edukt6-(3-Phenylamino-4-aminophenyl)oxyhexanoic acid methyl esterHCID 12043085—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt6-[[1-Phenyl-2-propylamino-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl EsterHCID 10200735—

Reaktionsschritte

200 mg of 6-(3-phenylamino-4-aminophenyl)oxyhexanoic acid methyl ester was dissolved in 2 ml of methanol, the solution was mixed with 90 μl of propylisothiocyanate, and the mixture was heated for 3 hours to 50° C. After cooling, it was mixed with saturated ammonium chloride solution, diluted with water, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 140 mg of a thiourea derivative, which was dissolved in 1.5 ml of methanol, was obtained. 0.16 ml of iodomethane was added to this solution, and it was refluxed for 4 hours. After cooling, it was mixed with IN aqueous hydrochloric acid, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 72 mg was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196202B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-f98b9b517ccf4f888b9a125c52b6dba9
Quellennotizuspto-grants-2007_03