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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912798Generated: October 25, 2026

1-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)piperazine → 4-Chloro-6-trifluoromethyl-2-[4-(3-chloro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl]-1H-benzoimidazole

https://huagongshe.com/reaction/912798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)piperazineHCID 667619—
Reactant1H-Benzimidazole, 2,7-dichloro-5-(trifluoromethyl)-HCID 66937336—
Product4-Chloro-6-trifluoromethyl-2-[4-(3-chloro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl]-1H-benzoimidazoleHCID 57835043—

Reaction Steps

The reaction of 1-(3-chloro-5-trifluoromethylpyridin-2-yl)piperazine (186 mg, 0.7 mmol, ABCR) and 2,4-dichloro-6-trifluoromethyl-1H-benzoimidazole (127 mg, 0.5 mmol, Example 5b) under the conditions of Example 3c afforded the title compound as a white amorphous solid. MS (ESI, pos. ion) m/z: 484 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026241B2
Source datasetuspto-grants-2011_09
ORD IDord-6c8706987f814c4fbde0a78460514c15
Source noteuspto-grants-2011_09