HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788608Generated: October 30, 2026
Hydrochloric Acid → 2-[2-[8-(4-chlorophenyl)-3,4-dihydro-2H-1,5-benzodioxepin-7-yl]-6-quinolyl]-1-cyclohexyl-benzimidazole-5-carboxylic acid
https://huagongshe.com/reaction/1788608
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-[8-(4-Chloro-phenyl)-3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl]-ethanone | HCID 68924261 | — |
| Reactant | 2-(4-amino-3-formyl-phenyl)-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid ethyl ester | HCID 86600382 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[2-[8-(4-chlorophenyl)-3,4-dihydro-2H-1,5-benzodioxepin-7-yl]-6-quinolyl]-1-cyclohexyl-benzimidazole-5-carboxylic acid | HCID 5276150 | 83.8% |
Reaction Steps
1-[8-(4-Chloro-phenyl)-3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl]-ethanone (76 mg, 0.25 mmol) and 2-(4-amino-3-formyl-phenyl)-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid ethyl ester (98 mg, 0.25 mmol) were dissolved in 500 μL ethanol and 500 μL 10% ethanolic KOH were added. The reaction was stirred at 75° C. overnight. The reaction was acidified with 4N hydrochloric acid, extracted three times with ethyl acetate, the organic extracts were dried with sodium sulfate and then evaporated. Purification via reverse-phase HPLC gave 132 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511145B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-c81dd56e7d224caf9b58cfef39785b59 |
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| Source note | uspto-grants-2009_03 |
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