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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazoleHCID 18630847—
Reactant(+/-)-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidineHCID 18630855—
SolventDichloromethaneHCID 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)piperidineHCID 1551328540%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521621B1
Source datasetuspto-grants-2003_02
ORD IDord-79f703350cd146d88e2ae858626043b5
Source noteuspto-grants-2003_02