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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443866Generated: November 2, 2026

1-Benzoylpiperazine → HCID 5495826, compound

https://huagongshe.com/reaction/1443866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzoylpiperazineHCID 762654—
ReactantHCID 22893811HCID 22893811—
ProductHCID 5495826HCID 5495826—

Reaction Steps

Precursor 5k, 1-benzoyl-4-[(7-chloro-6-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a, starting from (7-chloro-6-azaindol-3-yl)-oxoacetic acid potassium salt, Precursor 4a, and 1-benzoylpiperazine. MS m/z: (M+H)+ calcd for C20H18ClN4O3: 397.11; found 396.97. HPLC retention time: 2.37 minutes (column F, gradient time=3 min, flow rate=4 ml/min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662823B2
Source datasetuspto-grants-2010_02
ORD IDord-ca4f2dbc0cb448498a5180340f0ef56b
Source noteuspto-grants-2010_02