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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823412Generated: October 26, 2026

Diethyl Ether → 4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamide

https://huagongshe.com/reaction/1823412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthylenediamineHCID 3301—
Reactant2-ChloropyridineHCID 7977—
ReactantDiisopropylethylamineHCID 81531—
ReactantN~1~-(Pyridin-2-yl)ethane-1,2-diamineHCID 410428—
ReactantHCID 178512433HCID 178512433—
SolventAcetonitrileHCID 6342—
Product4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamideHCID 22142834—

Reaction Steps

2-(2-Aminoethylamino)pyridine (prepared from 2-chloropyridine and ethylenediamine in accordance with the method described in T. Mega et al., 1988, Bull. Chem. Soc. Japan 61:4315, which is incorporated herein by reference) (6 mmol) was treated with benzotriazole carboxamidinium 4-methylbenzenesulfonatesulfonate (2.0 g, 6 mmol) and DIEA (1.05 ml, 6 mmol) in anhydrous acetonitrile (10 ml) for 65 hours. Ether (ca. 10 ml) was then added to this mixture. After 8 hours the white solid amino[2-(2-pyridylamino)ethyl]carboxamidinium 4-methylbenzenesulfonate was filtered off and dried in vacuo. The resulting guanidine (200 mg) was reacted with 100 mg of resin (21 hours, 90° C.) according to the method described in Example 10 (Resin method C), to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037918B2
Source datasetuspto-grants-2006_05
ORD IDord-72fd78dd8e7e4d33a874ee01adcf21df
Source noteuspto-grants-2006_05