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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362860Generated: October 29, 2026

Hydrochloric Acid → 2-{[5-(Methoxy)-2-({3-[2-(4-morpholinyl)ethyl]phenyl}amino)-4-pyrimidinyl]amino}benzamide

https://huagongshe.com/reaction/1362860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
Reactant3-(Morpholinoethyl)anilineHCID 23071561—
Reactant2-[(2-Chloro-5-methoxypyrimidin-4-yl)amino]benzamideHCID 57974191—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-{[5-(Methoxy)-2-({3-[2-(4-morpholinyl)ethyl]phenyl}amino)-4-pyrimidinyl]amino}benzamideHCID 57974137—

Reaction Conditions

Temperature100 °C

Reaction Steps

3-[2-(4-Morpholinyl)ethyl]aniline (103 mg; 0.5 mmoles) was dissolved in THF (2 mL) and treated with 1 mL of a solution of 1M HCl in ethyl ether. The mixture was stirred for 5 min and then concentrated in vacuo. The residue was treated with 2-{[2-chloro-5-(methoxy)-4-pyrimidinyl]amino}benzamide (139 mg; 0.5 mmoles) and isopropanol (4 mL). The suspension was stirred in a vial, which was sealed and heated at 100° C. for 24 h. Upon cooling, the solid was collected by filtration, washed with cold isopropanol and dried in vacuo to afford the desired product. MS: (M+H)+=449.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884098B2
Source datasetuspto-grants-2011_02
ORD IDord-4155b7125aaf4f85ba73c2655bf84b74
Source noteuspto-grants-2011_02