HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060194Generated: November 2, 2026
2-chloro-1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazole → (+/-)-cis-1-[3,5-bis(trifluoromethyl)-benzoyl]-4-[4-[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]-1-piperazinyl]-2-(phenylmethyl)piperidine
https://huagongshe.com/reaction/1060194
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-chloro-1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazole | HCID 18630847 | — |
| Reactant | (+/-)-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidine | HCID 18630855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+/-)-cis-1-[3,5-bis(trifluoromethyl)-benzoyl]-4-[4-[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]-1-piperazinyl]-2-(phenylmethyl)piperidine | HCID 15513285 | 40% |
Reaction Steps
Compound 15 (0.005 mol), 2-chloro-1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazole (0.005 mol) and Cupper (0.005 mol) were stirred at 140° C. for 2 hours. The mixture was cooled, dissolved in CH2Cl2, filtered and washed with CH2Cl2 and a diluted NH4OH solution. The organic layer was separated, washed with a diluted NH4OH solution, dried, filtered and the solvent was evaporated. The residue was purified over silica gel on a glass filter (eluent: CH2Cl2/CH3OH 100/0, 99.5/0.5, 99/1, 98.5/1.5 and 98/2). The pure fractions were collected and the solvent was evaporated. The residue was dried, yielding 1.42 g (40%) (±)-cis-1-[3,5-bis(trifluoromethyl)-benzoyl]-4-[4-[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]-1-piperazinyl]-2-(phenylmethyl)piperidine (compound 70).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521621B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-79f703350cd146d88e2ae858626043b5 |
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| Source note | uspto-grants-2003_02 |
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