HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352930Generated: October 25, 2026
2-Bromo-2'-acetonaphthone → 2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-4-(2-naphthyl)-1H-imidazole
https://huagongshe.com/reaction/1352930
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-2'-acetonaphthone | HCID 69179 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide | HCID 178504796 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-4-(2-naphthyl)-1H-imidazole | HCID 22148946 | 54% |
Reaction Steps
To a mixture of 4-chloro-N-(4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (400 mg, 1.29 mmol) and sodium bicarbonate (216 mg, 2.59 mmol) in isopropanol (30 mL), 2-bromo-2′-acetonaphthone (970 mg, 3.89 mmol) was added. After heating the reaction mixture at 80–85° 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 (1.2 g) was purified by chromatography (silica gel, hexane/ethyl acetate, 6/4) to give 2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-4-(2-naphthyl)-1H-imidazole (318 mg, 54%) as a pale yellow solid: mp 204–206° C. Anal Calc'd. for C26H19N2SO2Cl: C, 68.04; H, 4.17; N, 6.10; S, 6.99. Found: C, 67.65; H, 4.19; N, 5.96; S, 7.10.
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-53e4bba4b4be46a7b7ba14750bfbfa03 |
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| Source note | uspto-grants-2007_05 |
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