HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428991Generated: November 2, 2026
Diisopropylethylamine → N-(3 hydroxyadamant-1-yl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide
https://huagongshe.com/reaction/1428991
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Amino-1-adamantanol | HCID 658645 | — |
| Reactant | 2-Chloro-1,3-dimethylimidazolidin-1-ium;hexafluorophosphate | HCID 21868419 | — |
| Reactant | 2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxylic acid | HCID 54579222 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3 hydroxyadamant-1-yl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide | HCID 58695776 | 67.1% |
Reaction Steps
To a magnetically stirred solution of 2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxylic acid (0.66 gram, 0.00306 mol) in dichloromethane (35 ml) was successively added diisopropylethylamine (DIPEA) (3.1 ml), CIP (2-chloro-1,3-dimethylimidazolinium hexafluorophosphate). (2.55 gram) and 3-hydroxyadamantane amine (0.612 gram, 0.00366 mol). The resulting mixture was reacted at 20° C. for 16 hours and subsequently concentrated in vacuo. The resulting residue was taken up in dichloromethane and washed with 5% aqueous NaHCO3 solution. The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The resulting residue was purified by flash chromatography (dichoromethane/methanol=98/2 (v/v)) to give N-(3 hydroxyadamant-1-yl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide (0.75 gram, 67% yield). Rf (silica gel/dichoromethane/methanol=98/2 (v/v))˜0.6. Melting point: 215-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937184B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-1393384b68b146fdafa96a648774b271 |
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| Source note | uspto-grants-2015_01 |
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