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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411786Generated: October 31, 2026

(4-Bromophenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone → 3-Benzoyl-1-{4-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}-4-methylimidazolidin-2-one

https://huagongshe.com/reaction/2411786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Bromophenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanoneHCID 71252046—
Reactant1-Benzoyl-5-methylimidazolidin-2-oneHCID 71252755—
Product3-Benzoyl-1-{4-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}-4-methylimidazolidin-2-oneHCID 7125220416%

Reaction Steps

Using (4-bromophenyl) [4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone (150 mg) described in Preparation Example 165 and 1-benzoyl-5-methylimidazolidin-2-one (98 mg) described in Preparation Example 56 and by the reaction and treatment in the same manner as in Example 1, the title compound (32 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-c43c039e67e443b9bb87234bbb2d01bd
Source noteuspto-grants-2014_08