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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117342Generated: October 29, 2026

1-Methylpiperazine → HCID 22238133, compound

https://huagongshe.com/reaction/2117342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 22238145HCID 22238145—
ProductHCID 22238133HCID 2223813389%

Reaction Steps

In an analogous procedure to that described in the fifth paragraph of the portion of Note c) which is concerned with the preparation of starting materials, N-[3-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-chloro-2-nitrobenzamide was reacted with 1-methylpiperazine to give N-[3-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-(4-methylpiperazin-1-yl)-2-nitrobenzamide in 89% yield; NMR Spectrum: (DMSOd6) 2.2 (s, 3H), 2.41 (m, 4H), 3.5 (m, 8H), 3.71 (t, 4H), 7.07 (m, 3H), 7.31 (m, 3H), 7.48 (d, 1H), 8.03 (d, 1H), 8.16 (s, 1H), 8.26 (d, 1H), 10.35 (broad s, 1H), 10.44 (broad s, 1H); Mass Spectrum: M+H+ 546.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442704B2
Source datasetuspto-grants-2008_10
ORD IDord-ce849db084bb42d99f70d4089190876f
Source noteuspto-grants-2008_10