HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005519Generated: October 25, 2026
Triethylamine → 2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole
https://huagongshe.com/reaction/1005519
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1-Dibutoxycyclohexane | HCID 243718 | — |
| Reactant | (5-(3,5-Dichlorophenylthio)-1-ethyl-4-isopropyl-1H-imidazol-2-yl)methanol | HCID 473933 | — |
| Reactant | Pyridinium.p-toluenesulfonate | HCID 22033616 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole | HCID 53719220 | 34% |
Reaction Steps
To a solution of 2-hydroxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole (19) (345 mg, 1 mmol) prepared in accordance with the method as described in WO 96/10019 (EXAMPLE 25) and p-toluenesulfonic acid pyridinium (264 mg, 1.05 mmol) in methylene chloride (5 ml) was added 1,1-dibutoxycyclohexane (2.14 g, 10.0 mmol), and stirred at room temperature for 20 hours. A drop of triethylamine was added to the reaction mixture , and the mixture was filtered to remove the precipitated insoluble matter. The filtrate was concentrated under reduced pressure. Hexane was added to the residue, and the mixture was filtered to remove the insoluble matter. The filtrate was purified by chromatography on an alumina column (eluate: toluene) to give the compound 20 (165 mg, 34%). Rf 0.41 (Al2O3 60, Type E, toluene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054591 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-5b3f7ad41dbf4aa48d176520476b5aad |
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| Source note | uspto-grants-2000_04 |
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