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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117344Generated: October 31, 2026

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

https://huagongshe.com/reaction/2117344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-Dimethyl-1,3-propanediamineHCID 66978—
ReactantN-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-chloro-2-nitrobenzamideHCID 22238142—
ProductN-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl)-5-[N-(3-methylaminopropyl)-N-methylamino]-2-nitrobenzamideHCID 22238184—

Reaction Steps

In an analogous procedure to that described in the fifth paragraph of the portion of Note a) which is concerned with the preparation of starting materials, N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-5-chloro-2-nitrobenzamide was reacted with N-(3-methylaminopropyl)-N-methylamine to give N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl)-5-[N-(3-methylaminopropyl)-N-methylamino]-2-nitrobenzamide; NMR Spectrum: (DMSOd6) 1.61-1.74 (m, 2H), 2.35 (s, 3H), 2.26. (m, 3H), 2.38-2.44 (m, 2H), 3.09 (s, 3H), 3.5-3.55 (m, 6H), 3.7-3.74 (m, 4H), 6.78 (s, 1H), 6.84 (d, 1H), 7.14 (d, 1H), 7.21 (d, 1H), 7.27 (s, 1H), 7.6 (d, 1H), 7.9 (s, 1H), 8.04 (d, 1H), 8.27 (d, 1H), 9.83 (s, 1H), 10.55 (s, 1H); Mass Spectrum: M+H+ 562.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442704B2
Source datasetuspto-grants-2008_10
ORD IDord-c2051f15b7ab4816b097f6d39294f3b2
Source noteuspto-grants-2008_10