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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17644Generated: October 29, 2026

3-(3-Tert-butylphenoxy)benzaldehyde → 1-butyl-2-{3-[3-tert-butyl-phenoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole

https://huagongshe.com/reaction/17644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-Tert-butylphenoxy)benzaldehydeHCID 63943447—
Reactant1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazineHCID 66977666—
Product1-butyl-2-{3-[3-tert-butyl-phenoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazoleHCID 59699164—

Reaction Steps

A mixture of 1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazine (synthesized via General Procedures G1 and G2 and H) (0.130 g, 0.512 mmol) and 3-(3-tert-butylphenoxy)benzaldehyde was subjected to General Procedure K. Reaction was concentrated and purified on silica gel chromatography using DCM-2% MeOH/DCM. The BOC-group was removed employing General Procedure T1 to give 1-butyl-2-{3-[3-tert-butyl-phenoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole (0.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737285B2
Source datasetuspto-grants-2010_06
ORD IDord-a15e7e8b3593451ba01747a6def22a18
Source noteuspto-grants-2010_06