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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12137Generated: October 27, 2026

Triethylamine → N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl} (4-{[(1-methyl(2-imidazolin-2-yl))amino]methyl}phenyl)carboxamide

https://huagongshe.com/reaction/12137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-methyl-2-methylsulfanyl-4,5-dihydro-1H-imidazoleHCID 10396874—
Reactant[4-(Aminomethyl)phenyl]-n-{2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamideHCID 18727608—
SolventPyridineHCID 1049—
ProductN-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl} (4-{[(1-methyl(2-imidazolin-2-yl))amino]methyl}phenyl)carboxamideHCID 2259637965%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of [4-(aminomethyl)phenyl]-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide (74 mg, 0.195 mmol), 1-methyl-2-methylthio-2-imidazoline (25 mg, 0.195 mmol), NEt3 (2 mL) and pyridine (5 mL) was stirred at 80° C. overnight, concentrated and HPLC (C18 reversed phase) eluting with 0.1% TFA in H2O/CH3CN gave N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}(4-{[(1-methyl(2-imidazolin-2-yl))amino]methyl}phenyl)carboxamide (52 mg, 65%). MS found for C24H23ClN6O2 (M+H)+: 463.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727982B2
Source datasetuspto-grants-2010_06
ORD IDord-abaf463b08694e7e97c7286f7583efbb
Source noteuspto-grants-2010_06