Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783573Generated: October 29, 2026

(R)-1-Benzoyl-3-methylpiperazine → HCID 59693973, compound

https://huagongshe.com/reaction/1783573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-1-Benzoyl-3-methylpiperazineHCID 7578227—
ReactantHCID 59693965HCID 59693965—
ProductHCID 59693973HCID 59693973—

Reaction Steps

Precursor 5f, 1-benzoyl-3-(R)-methyl-4-[(7-bromo-6-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a, starting from (7-bromo-6-azaindol-3-yl)-oxoacetic acid potassium salt, Precursor 4g, and 1-benzoyl-3-(R)-methylpiperazine. MS m/z: (M+H)+ calcd for C21H20BrN4O3: 455.07; found 455.14. HPLC retention time: 1.45 minutes (column B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501420B2
Source datasetuspto-grants-2009_03
ORD IDord-52687537d26442759399f73147a374df
Source noteuspto-grants-2009_03