Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101719Generated: October 26, 2026

1-Aminopiperidine → N-(Piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamide

https://huagongshe.com/reaction/2101719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AminopiperidineHCID 16658—
ReactantEthyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylateHCID 22066075—
ProductN-(Piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamideHCID 10183243—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of ethyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylate (50 mg, 0.125 mmol) from Step D in neat 1-aminopiperidine (1 mL) was heated at 90° C. for 72 hr. Most of the amine was evaporated under a stream of nitrogen and the residue was purified by Prep TLC (2×1 mm, silica) (40% ethyl acetate in hexanes to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572785B2
Source datasetuspto-grants-2009_08
ORD IDord-32a9b6ea237a4719b9ecba72c5ce1b06
Source noteuspto-grants-2009_08