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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Amino-1,2,2,6,6-pentamethylpiperidine | HCID 693792 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 5,6-Dichloro-2-(4-carboxy-2-methoxyphenyl)benzimidazole | HCID 21101166 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | 4-(5,6-Dichlorobenzimidazol-2-yl)-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)-3-methoxybenzamide | HCID 9913417 | 47.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220769B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-af7ad8f0a1dc42b390a8d59218c54b8b |
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| Source note | uspto-grants-2007_05 |
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