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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236966Generated: October 26, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate

https://huagongshe.com/reaction/2236966

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
Reactant2-Butylamino-4,6-di(3-diethylaminopropoxy)anilineHCID 66977544—
SolventEthanolHCID 702—
Producttert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylateHCID 6697750669%

Reaction Steps

A solution of 1-(t-butyloxycarbonyl)piperdine-4-carboxaldehyde (235 mg; 1.1 mmol) and 2-butylamino-4,6-di(3-diethylaminopropoxy)aniline (synthesized via General Procedures J1 and J2 and I) (424 mg; 1 mmol) in ethanol (5 mL) was subjected to General Procedure K. The crude product was purified by silica gel column chromatography using 10% MeOH in DCM with a gradual increment of triethylamine (0.2 to 1.0%) as eluent to afford 425 mg of tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714013B2
Source datasetuspto-grants-2010_05
ORD IDord-da305e2f10684516a0b5ace39de31406
Source noteuspto-grants-2010_05