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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281729Generated: November 1, 2026

N,N-Dimethyl-1,3-propanediamine → N-[2-methyl-5(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-(3-dimethylaminopropylamino)-2-nitrobenzamide

https://huagongshe.com/reaction/1281729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantN-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-chloro-2-nitrobenzamideHCID 22238142—
ProductN-[2-methyl-5(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-(3-dimethylaminopropylamino)-2-nitrobenzamideHCID 18422107—

Reaction Steps

In an analogous procedure to that described in Example 15, N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-chloro-2-nitrobenzamide was reacted with 3-dimethylaminopropylamine to give the title compound; NMR Spectrum: (DMSOd6) 1.6-1.72 (m, 2H), 2.12 (s, 6H), 2.22-2.28 (m, 5H), 3.2-3.25 (m, 2H), 3.5-3.54 (m, 4H), 3.69-3.73 (m, 4H), 6.65-6.68 (m, 2H), 7.04 (d, 1H), 7.2 (d, 1H), 7.25 (d, 1H), 7.29 (t, 1H), 7.68 (d, 1H), 8.84 (s, 1H), 8.0 (d, 1H), 8.26 (d, 1H), 9.82 (s, 1H), 10.34 (s, 1H); Mass Spectrum: M+H+ 562.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455520B1
Source datasetuspto-grants-2002_09
ORD IDord-7dbb71afd0e547a79dd6cbea326b5df8
Source noteuspto-grants-2002_09