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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101692Generated: October 30, 2026

Piperidine → N-(Piperidin-1-yl)-4,5-di(4-methylphenyl)-1-methylimidazole-2-carboxamide

https://huagongshe.com/reaction/2101692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1-AminopiperidineHCID 16658—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
ReactantHCID 22066080HCID 22066080—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(Piperidin-1-yl)-4,5-di(4-methylphenyl)-1-methylimidazole-2-carboxamideHCID 1015711932.2%

Reaction Steps

A mixture of 4,5-di-(4-methylphenyl)-1-methylimidazole-2-carboxylic acid (25 mg, 0.08 mmol) from Step A, 1-aminopiperidine (0.020 mL, 0.16 mmol) (containing a small percent of piperidine as an impurity), PyBOP (NovaChem) (65 mg, 0.1 mmol) and DIPEA (0.025 mL, 0.1 mmol) in methylene chloride (1 mL) was stirred at rt for 20 hr. The reaction was diluted with water and extracted twice with methylene chloride. The organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified twice by prep TLC (1 mm, silica gel) eluting with 5% methylene chloride, 35% ethyl acetate in hexanes to afford the primary product N-(piperidin-1-yl)-4,5-di-(4-methylphenyl)-1-methylimidazole-2-carboxamide (10 mg, 32%) and 2-(piperidin-1-ylcarbonyl)-4,5-di-(4-methylphenyl)-1-methylimidazole as a byproduct.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572785B2
Source datasetuspto-grants-2009_08
ORD IDord-72cf6bec0a634632bec0e6ff280f84cd
Source noteuspto-grants-2009_08