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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80241Generated: October 26, 2026

1,2-Diaminocyclohexane → 1-Benzothiazol-6-yl-3-(4-chloro-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/80241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiaminocyclohexaneHCID 4610—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Bromo-4-chloropyridineHCID 817696—
Reactant1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 66678554—
CatalystCopper iodideHCID 83717—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
Product1-Benzothiazol-6-yl-3-(4-chloro-pyridin-3-yl)-imidazolidin-2-oneHCID 5963622160%

Reaction Steps

Using the same reaction conditions and work up as described in Example 1, step-3,1-benzothiazol-6-yl-imidazolidin-2-one (I-84b: 800 mg, 3.653 mmol) was refluxed with 3-bromo-4-chloro-pyridine (879 mg, 4.566 mmol), copper iodide (70 mg, 0.365 mmol), cyclohexane-1,2-diamine (125 mg, 1.0958 mmol), potassium phosphate (2.32 g, 10.958 mmol) and 1,4-Dioxane (50 mL) at 110° C. for 12 hours to afford the crude product. The reaction was monitored by TLC (10% MeOH in chloroform). Purification by column chromatography on silica gel (1.5% methanol in chloroform) afforded 715 mg of the product (60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045173E1
Source datasetuspto-grants-2014_09
ORD IDord-800efc2c8ea84b14949952a612a07b65
Source noteuspto-grants-2014_09