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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302264Generated: October 26, 2026

1,3-Propanediamine, N1,N1,N3-trimethyl- → N-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-6-[N-(3-dimethylaminopropyl)-N-methylamino]pyridine-3-carboxamide

https://huagongshe.com/reaction/2302264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N1,N1,N3-trimethyl-HCID 78302—
Reactant6-chloro-N-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-3-carboxamideHCID 22057943—
ProductN-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-6-[N-(3-dimethylaminopropyl)-N-methylamino]pyridine-3-carboxamideHCID 2205800773%

Reaction Steps

Using an analogous procedure to that described in Example 21, 6-chloro-N-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-3-carboxamide was reacted with N-(3-dimethylaminopropyl)-N-methylamine to give the title compound in 73% yield; NMR Spectrum: (DMSOd6) 1.67 (m, 2H), 2.12 (s, 6H), 2.21 (t, 2H), 3.07 (s, 3H), 3.51 (m, 4H), 3.58 (m, 2H), 3.71 (m, 4H), 6.69 (d, 1H), 7.1 (d, 1H), 7.23 (s, 1H), 7.5 (d, 1H), 8.04 (m, 2H), 8.28 (d, 1H), 8.72 (s, 1H), 9.7 (s, 1H), 10.44 (s, 1H); Mass Spectrum: M+H+ 552 and 554.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432949B1
Source datasetuspto-grants-2002_08
ORD IDord-493acaf1a686472fa18356b76cba6280
Source noteuspto-grants-2002_08