HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352933Generated: October 25, 2026
Bromomethyl 4-methoxyphenyl ketone → 2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-(4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazole
https://huagongshe.com/reaction/1352933
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide | HCID 178504796 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-(4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazole | HCID 22998078 | 113.4% |
Reaction Steps
To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (700 mg, 2.24 mmol) and sodium bicarbonate (376 mg, 4.48 mmol) in isopropanol (50 mL), 4-methoxyphenacyl bromide (1.03 g, 4.48 mmol) was added. After, heating the reaction mixture at 75–80° C. for 20 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by chromatography (silica gel, hexane/ethyl acetate, 6/4) to give 2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-[4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazole (695 mg, 71%) as a white solid: mp 110–113° C. Anal Calc'd. for C23H19N2SO3Cl: C, 62.94; H, 4.36; N, 6.38; S, 7.30. Found: C, 62.54; H, 4.43; N, 6.17; S, 7.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220770B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-a04503fffbe14927a59646211b786705 |
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| Source note | uspto-grants-2007_05 |
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