Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828742Generated: November 3, 2026

1,2-Ethanediamine, N1,N1,N2-trimethyl- → 2-[N-(2-dimethylaminoethyl)-N-methylamino]-N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamide

https://huagongshe.com/reaction/1828742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Reactant2-chloro-N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamideHCID 22057950—
Product2-[N-(2-dimethylaminoethyl)-N-methylamino]-N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamideHCID 2205799844%

Reaction Steps

Using an analogous procedure to that described in Example 21, 2-chloro-N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]pyridine-4-carboxamide was reacted with N-(2-dimethylaminoethyl)-N-methylamine to give the title compound in 44% yield; NMR Spectrum: (DMSOd6) 2.17 (s, 6H), 2.19 (s, 3H), 2.4 (t, 2H), 3.05 (s, 3H), 3.5-3.54 (m, 4H) 3.65-3.72 (m, 6H), 6.75 (s, 1H), 6.94 (d, 1H), 7.02 (s, 1H), 7.1 (d, 1H), 7.24 (d, 2H), 7.58 (d, 1H), 7.78 (s, 1H), 8.19 (d, 1H), 8.26 (d, 1H), 9.96 (s, 1H), 10.28 (s, 1H); Mass Spectrum: M+H+ 518.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060700B2
Source datasetuspto-grants-2006_06
ORD IDord-05ec7d0061064472b75c7538e7ec27e7
Source noteuspto-grants-2006_06