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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828741Generated: October 25, 2026

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

https://huagongshe.com/reaction/1828741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N1,N1,N3-trimethyl-HCID 78302—
Reactant2-chloro-N-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamideHCID 22057982—
ProductN-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-2-[N-(3-dimethylaminopropyl)-N-methylamino]pyridine-4-carboxamideHCID 2205797046%

Reaction Steps

Using an analogous procedure to that described in Example 21, 2-chloro-N-[2-chloro-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamide was reacted with N-(3-dimethylaminopropyl)-N-methylamine to give the title compound in 46% yield; NMR Spectrum: (DMSOd6) 1.67 (m, 2H), 2.11 (s, 6H), 2.21 (m, 2H), 3.04 (s, 3H), 3.51 (m, 6H), 3.71 (m, 4H), 6.97 (d, 1H), 7.09 (m, 2H), 7.23 (s, 1H), 7.54 (d, 1H), 7.71 (d, 1H), 8.04 (s, 1H), 8.20 (d, 1H), 8.27 (d, 1H), 10.13 (s, 1H), 10.47 (s, 1H); Mass Spectrum: M+H+ 552.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060700B2
Source datasetuspto-grants-2006_06
ORD IDord-72687da26b9c4defbb9e09bcf148755c
Source noteuspto-grants-2006_06