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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563150Generated: October 31, 2026

Potassium Carbonate → HCID 67004780, compound

https://huagongshe.com/reaction/563150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-PyrrolidoneHCID 12025—
ReactantHCID 86623404HCID 86623404—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67004780HCID 6700478052%

Reaction Conditions

Temperature120 °C

Reaction Steps

In an inert atmosphere, N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(6-bromo-pyridin-3-ylmethyl)-3-(4-trifluoromethyl-phenyl)-acrylamide (70 mg, 0.101 mmol), 2-pyrrolidinon (10.3 mg, 0.121 mmol), potassium carbonate (27.9 mg, 0.202 mmol), copper(I)iodide (1 mg, 0.005 mmol) and N,N-dimethylenediamine (1 mg, 0.01 mmol) were dissolved in dioxane (1 mL). The reaction mixture was heated to 120° C. for 12 h, then filtered over a plug of silicagel with EtOAc, concentrated and purified by perp. HPLC to give 29 mg (52%) of N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-[6-(2-oxo-pyrrolidin-1-yl)-pyridin-3-ylmethyl]-3-(4-trifluoromethyl-phenyl)-acrylamide. (LC-MS: tR=1.02 min; [M+H]+=688.46).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067419B2
Source datasetuspto-grants-2011_11
ORD IDord-6a58f10a75f042b0aba9dd44a1615cf8
Source noteuspto-grants-2011_11