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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2110001Erstellt: 25. Oktober 2026

Methanol → 2-{[1-(3,5-dichloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2110001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt3,5-DichlorosalicylaldehydeHCID 66660—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt2-[(piperidin-4-ylmethyl)-amino]-1H-benzimidazole-4-carboxylic acid methyl esterHCID 69067985—
LösungsmittelDimethylsulfoxide acetic acidHCID 18355466—
Produkt2-{[1-(3,5-dichloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid methyl esterHCID 10195352—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

After dissolving 2-[(piperidin-4-ylmethyl)-amino]-1H-benzimidazole-4-carboxylic acid methyl ester (20 mg, 0.055 mmol) in dimethylsulfoxide-acetic acid (10:1), 2-hydroxy-3,5-dichlorobenzaldehyde (32.0 mg, 0.166 mmol) and sodium triacetoxyborohydride (35.0 mg, 0.166 mg) were added and the mixture was stirred at 50° C. for 2 days. Methanol (1 ml) was added to the reaction mixture, and then after stirring for 1 minute, it was purified by SCX solid phase extraction (Bond Elute SCX500MG). The product was further purified by preparative HPLC to obtain 2-{[1-(3,5-dichloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid methyl ester. The compound was identified by LC-MS.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07517875B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-432aaa06404b40bea99d45bff01826f0
Quellennotizuspto-grants-2009_04