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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783582Generated: October 30, 2026

1-Benzoylpiperazine → HCID 59693829, compound

https://huagongshe.com/reaction/1783582

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzoylpiperazineHCID 762654—
ReactantHCID 67152743HCID 67152743—
ProductHCID 59693829HCID 59693829—

Reaction Steps

Precursor 5p, 1-benzoyl-4-[(7-chloro-4-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a starting from Potassium (7-chloro-4-fluoro-4-azaindol-3-yl)oxoacetate, Precursor 4e, and 1-benzoyl-piperazine. 1H NMR (500 MHz, CD3OD) δ8.83 (s, 1H), 8.63 (d, 1H, J=5.35 Hz), 7.91 (d, 1H, J=5.75 Hz), 7.47 (m, 5H), 3.80-3.30 (m, 3H). MS m/z: (M+H)+ Calc'd for C20H18ClN4O3: 397.11; Found 397.02. HPLC retention time: 1.20 minutes (column A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501420B2
Source datasetuspto-grants-2009_03
ORD IDord-3a278e3741de400eb1c76860d7c67d07
Source noteuspto-grants-2009_03