Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383974Generated: October 27, 2026

Dicyclohexylcarbodiimide → 1-[3-[3-(Piperidin-1-yl)propylcarbamoyl]butyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazole

https://huagongshe.com/reaction/1383974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPiperidine-1-propylamineHCID 19049—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(3-Carboxybutyl)-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazoleHCID 21188512—
SolventDimethylformamideHCID 6228—
Product1-[3-[3-(Piperidin-1-yl)propylcarbamoyl]butyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazoleHCID 21188479125.7%

Reaction Steps

To a stirring solution of 1-[3-carboxybutyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazole (1.2 g, 3.2 mmol) in N,N-dimethylformamide (75 ml) were added sequentially 1-amino-3-(piperidin-1-yl)propane (500 mg, 1.1 eq), 1-hydroxybenzotriazole (475 mg, 1.1 eq), and dicyclohexylcarbodiimide (726 mg, 1.1 eq). The resulting mixture was then stirred under a nitrogen atmosphere at room temperature for 64 hours. The reaction mixture was then filtered and the resulting filtrate was concntrated under reduced pressure. This residue was taken into ethyl acetate (200 ml) and washed once with water (200 ml), dried over potassium carbonate. The solvents were removed in vacuo to yield 2.00 grams of a semi-solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255494B1
Source datasetuspto-grants-2001_07
ORD IDord-4d1e0e0d00914703b078d61615c5a1e9
Source noteuspto-grants-2001_07