HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368524Generated: November 1, 2026
Triethylamine → ethyl 2-(((2,6-dichlorophenyl)thio)methyl)-1-(4-fluorophenyl)-1H-imidazole-5-carboxylate
https://huagongshe.com/reaction/2368524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzenethiol, 2,6-dichloro- | HCID 90671 | — |
| Reactant | ethyl 1-(4-fluorophenyl)-2-(hydroxymethyl)-1H-imidazole-5-carboxylate | HCID 71117501 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-(((2,6-dichlorophenyl)thio)methyl)-1-(4-fluorophenyl)-1H-imidazole-5-carboxylate | HCID 71117764 | — |
Reaction Steps
To a solution of ethyl 1-(4-fluorophenyl)-2-(hydroxymethyl)-1H-imidazole-5-carboxylate (15) (1.25 g, 4.7 mmol) and triethylamine (0.95 g, 9.4 mmol) in CH2Cl2 (30 mL) was added methanesulfonyl chloride (0.65 g, 5.64 mmol) at 0° C. and the reaction was stirred at 0° C. After 3 hours, 2,6-dichlorobenzenethiol (0.84 g mg, 4.7 mmol) and cesium carbonate (2.28 g, 7 mmol) were added and the reaction was stirred at room temperature for 1 hour. The mixture was filtered by vacuum filtration, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to afford ethyl 2-(((2,6-dichlorophenyl)thio)methyl)-1-(4-fluorophenyl)-1H-imidazole-5-carboxylate (72).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08703776B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-eeb36889033e49a186a801857ce3a5d5 |
|---|
| Source note | uspto-grants-2014_04 |
|---|