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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1-Aminopiperidine | HCID 16658 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 22066080 | HCID 22066080 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(Piperidin-1-yl)-4,5-di(4-methylphenyl)-1-methylimidazole-2-carboxamide | HCID 10157119 | 32.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572785B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-72cf6bec0a634632bec0e6ff280f84cd |
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| Source note | uspto-grants-2009_08 |
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