HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047374Generated: November 1, 2026
Cyclopropanecarboxylic acid → cyclopropyl-{4-[3-(1-methyl-1H-benzoimidazol-2-yl)-phenyl]-piperazin-1-yl}-methanone
https://huagongshe.com/reaction/2047374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1-Methyl-2-(3-piperazin-1-yl-phenyl)-1H-benzoimidazole dihydrochloride | HCID 68670433 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | cyclopropyl-{4-[3-(1-methyl-1H-benzoimidazol-2-yl)-phenyl]-piperazin-1-yl}-methanone | HCID 68671116 | 85.8% |
Reaction Steps
To a solution of cyclopropanecarboxylic acid (0.06 g, 0.68 mmol) in acetonitrile (8 mL) was added CDI (0.11 g, 0.68 mmol) and the resulting suspension was stirred at room temperature for 5 h. 1-Methyl-2-(3-piperazin-1-yl-phenyl)-1H-benzoimidazole dihydrochloride (0.20 g, 0.55 mmol) was added and the resulting solution heated at 65° C. overnight. The reaction was then cooled to room temperature, the solvent removed under reduced pressure. The crude product was redissolved in dichloromethane (15 mL) and washed with saturated NaHCO3 solution (2×3 mL) The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (eluent: cyclohexane:EtOAc, gradient from 100% cyclohexane to 100% ethyl acetate) to afford 0.17 g (85%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592463B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-1c01f9252fe94edeb073a4b3f83cbbce |
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| Source note | uspto-grants-2013_11 |
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