Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245940Generated: November 1, 2026

Potassium Carbonate → HCID 24829800, compound

https://huagongshe.com/reaction/2245940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-PyrrolidoneHCID 12025—
Reactant(1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamineHCID 13822957—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 24831567HCID 24831567—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 24829800HCID 24829800—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 6-(4-bromophenyl)-3-[1-(4-methoxyphenyl)cyclopropyl][1,2,4]-triazolo[4,3-b][1,2,4]triazine (Example 17, isomer-I, 25.3 mg, 0.0600 mmol), 2-Pyrrolidinone (5.47 μL, 0.0720 mmol), (1S,2S)—N,N′-dimethylcyclohexane-1,2-diamine (1.9 μL, 0.012 mmol), copper(I) iodide (1.14 mg, 0.00600 mmol), and potassium carbonate (17.4 mg, 0.126 mmol) in 1,4-dioxane (0.75 mL) was cooled (dry-ice acetone bath), purged in vacuo, and charged with nitrogen. Then the mixture was heated at 150° C. for 4 h. After cooling, the mixture was diluted with methanol. The resulting solution was purified by RP-HPLC (pH=10) to give the desired product. Analytical LCMS: (M+H)+=427.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683060B2
Source datasetuspto-grants-2010_03
ORD IDord-6cb01e94a6154db9bc15bf16f784d28a
Source noteuspto-grants-2010_03