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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557253Generated: October 27, 2026

N-(2-chloroethyl)-2-methyl-3-hydroxy-4-pyridinone → N-(4-propargylpiperazin-1-ylethyl)-2-methyl-3-hydroxy-4-pyridinone

https://huagongshe.com/reaction/557253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-chloroethyl)-2-methyl-3-hydroxy-4-pyridinoneHCID 337279—
Reactant1-(2-Propynyl)piperazineHCID 14627369—
ProductN-(4-propargylpiperazin-1-ylethyl)-2-methyl-3-hydroxy-4-pyridinoneHCID 58730241—

Reaction Steps

The title compound was prepared as described in Scheme D by reaction of N-(2-chloroethyl)-2-methyl-3-hydroxy-4-pyridinone (H2, Appendix VII) (prepared as described in Bijaya L. Rai, Lotfollah Dekhordi, Hicham Khodr, Yi Jin, Zudong Liu, and Robert C. Hider J. Med. Chem. 1998, 41,3347-3359) with N-propargylpiperazine (obtained as in step (iii) in Example 2):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058442B2
Source datasetuspto-grants-2011_11
ORD IDord-194915e88a1a4046b094fe8c00e075a1
Source noteuspto-grants-2011_11