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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352665Generated: November 1, 2026

4-Amino-1,2,2,6,6-pentamethylpiperidine → 4-(5,6-Dichlorobenzimidazol-2-yl)-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)-3-methoxybenzamide

https://huagongshe.com/reaction/1352665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1,2,2,6,6-pentamethylpiperidineHCID 693792—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5,6-Dichloro-2-(4-carboxy-2-methoxyphenyl)benzimidazoleHCID 21101166—
SolventTetrahydrofuranHCID 8028—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product4-(5,6-Dichlorobenzimidazol-2-yl)-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)-3-methoxybenzamideHCID 991341747.6%

Reaction Steps

A solution of 5,6-dichloro-2-(4-carboxy-2-methoxyphenyl)benzimidazole (0.8 g, 2,36 mmol), prepared as described in Preparation 6,1-hydroxybenzotriazole (0.32 g, 2.36 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.56 g, 2.9 mmol) in 80 ml of DMF/THF (50:50) was refluxed for 5 h. A solution of 1,2,2,6,6-pentamethyl-4-aminopiperidine (0.5 g, 2.9 mmol) in THF (5 ml) was added dropwise and the reaction was refluxed for additional 3 h. After cooling, solvent was removed under reduced pressure and the residue was treated with 1N NaOH (10 ml) and extracted with dichloromethane (50 ml). The organic layer was washed with water, dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was triturated with diisopropyl ether (150 ml), stirred for 1 h, filtered to give 0.55 g of the title compound (yield 47.6%), mp=285–286° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220769B2
Source datasetuspto-grants-2007_05
ORD IDord-af7ad8f0a1dc42b390a8d59218c54b8b
Source noteuspto-grants-2007_05