Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80220Generated: October 25, 2026

Potassium Phosphate, Tribasic → 1-Benzothiazol-6-yl-4-methyl-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/80220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Reactant3-Iodo-4-methylpyridineHCID 14423513—
Reactant1-Benzothiazol-6-yl-4-methyl-imidazolidin-2-oneHCID 59636211—
CatalystCopper iodideHCID 83717—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
Product1-Benzothiazol-6-yl-4-methyl-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 4987196116.66%

Reaction Steps

Using the same reaction conditions and work up as described in Example 1, step-3,1-benzothiazol-6-yl-4-methyl-imidazolidin-2-one (I-167b: 150 mg, 0.643 mmol) was refluxed with 3-iodo-4-methyl-pyridine (155 mg, 0.708 mmol), copper iodide (12.21 mg, 0.0643 mmol), N,N′-dimethyl-cyclohexane-1,2-diamine (27.39 mg, 0.192 mmol), potassium phosphate (341.5 mg, 1.607 mmol) and 1,4-dioxane (5 mL) at 120° 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 (3% methanol in chloroform) followed by preparative HPLC afforded 34 mg of the product (16.66% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045173E1
Source datasetuspto-grants-2014_09
ORD IDord-c7f55d5db3414a5da3720921e0304c55
Source noteuspto-grants-2014_09