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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281728Generated: October 27, 2026

1-Methylpiperazine → N-[2-methyl-5(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-3-(4methylpiperazin-1-yl)-2-nitrobenzamide

https://huagongshe.com/reaction/1281728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantN-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-3-chloro-2-nitrobenzamideHCID 22238140—
ProductN-[2-methyl-5(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-3-(4methylpiperazin-1-yl)-2-nitrobenzamideHCID 18422090—

Reaction Steps

In an analogous procedure to that described in Example 15, N-[2-methyl-5-(2-morpholinopyrid-4ylcarbonylamino)phenyl]-3-chloro-2-nitrobenzamide was reacted with 1-methylpiperazine to give the title compound; NMR Spectrum: (DMSOd6) 2.84-2.89 (m, 4H), 2.92-3.08 (m, 4H), 3.58-3.61 (m, 4H), 3.81-3.84 (m, 4H), 6.95 (d, 1H), 7.09 (s, 1H), 7.10 (d, 1H), 7.41-7.44 (m, 2H), 7.53 (d, 1H), 7.76 (d, 1H), 7.96 (s, 1H), 8.04 (s, 1H), 8.3 (d, 1H); Mass Spectrum: M+H+ 560.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455520B1
Source datasetuspto-grants-2002_09
ORD IDord-2707102379fb413fa493256d929da9fb
Source noteuspto-grants-2002_09