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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80156Generated: October 30, 2026

1,2-Diaminocyclohexane, trans- → HCID 68782383, compound

https://huagongshe.com/reaction/80156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-(4-Methylpyridin-3-yl)imidazolidin-2-oneHCID 59636170—
ReactantHCID 67078557HCID 67078557—
CatalystCopper iodideHCID 83717—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68782383HCID 6878238367.71%

Reaction Steps

Using the same reaction conditions as in Example 18, 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 0.108 g, 0.0006 mol) was reacted with 5-bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-b]pyridine (0.2 g, 0.0006 mol), 1,4-dioxane (20 mL), copper iodide (6.011 g, 0.00006 mol), trans-1,2-diamino cyclohexane (0.020 g, 0.00018 mol) and potassium phosphate (0.254 g, 0.0012 mol) to afford the crude product. Purification by column chromatography on silica gel (15% MeOH in CHCl3) afforded 172 mg of 1-(4-Methyl-pyridin-3-yl)-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]-imidazolidin-2-one (67.71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045173E1
Source datasetuspto-grants-2014_09
ORD IDord-5d495adbbb13469bb416f528f962026e
Source noteuspto-grants-2014_09