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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17645Generated: October 29, 2026

1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazine → 1-butyl-2-(4-[2-(4-chlorophenyl)ethoxy]-phenyl)-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole

https://huagongshe.com/reaction/17645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazineHCID 66977666—
Reactant4-[2-(4-Chlorophenyl)ethoxy]benzaldehydeHCID 71350669—
Product1-butyl-2-(4-[2-(4-chlorophenyl)ethoxy]-phenyl)-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazoleHCID 5969914659.6%

Reaction Steps

A mixture of 4-[2-(4-chloro-phenyl)-ethoxy]-benzaldehyde (0.08 g)and 1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazine (0.10 g) was subjected to General Procedure K. Ethanol was removed in vacuo and the residue purified on silica gel with 1-2% MeOH/DCM. The BOC-group was removed employing General Procedure T1 to give 1-butyl-2-{4-[2-(4-chlorophenyl)ethoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole (0.081 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737285B2
Source datasetuspto-grants-2010_06
ORD IDord-eca42764dd114ce49ad583c5931465c2
Source noteuspto-grants-2010_06