Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383896Generated: November 2, 2026

1,2-Diaminocyclohexane, trans- → 1-(4-Methylpyridin-3-yl)-3-(quinolin-7-yl)imidazolidin-2-one

https://huagongshe.com/reaction/2383896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant7-BromoquinolineHCID 521259—
Reactant1-(4-Methylpyridin-3-yl)imidazolidin-2-oneHCID 59636170—
CatalystCopper iodideHCID 83717—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Methylpyridin-3-yl)-3-(quinolin-7-yl)imidazolidin-2-oneHCID 4987284365.3%

Reaction Steps

Using the same reaction conditions as described in example 14, 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 116 mg, 0.6554 mmol) was reacted with 7-bromo-quinoline (150 mg, 0.72098 mmol), 1,4-dioxane (50 mL), copper iodide (12.4 mg, 0.06554 mmol), trans-1,2-diamino cyclohexane (22.5 mg, 0.19638 mmol) and potassium phosphate (347.3 g, 1.6365 mmol) to afford the crude product. Purification by column chromatography on silica gel (2% MeOH in CHCl3) afforded 130 mg of the product (65.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263635B2
Source datasetuspto-grants-2012_09
ORD IDord-8d97ae46abe94521affa4c72c4fe697b
Source noteuspto-grants-2012_09