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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579162Generated: October 26, 2026

Potassium Carbonate → HCID 66685270, compound

https://huagongshe.com/reaction/579162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
ReactantMethyl 3-bromo-5-phenyl-thiophene-2-carboxylateHCID 20775762—
ReactantHCID 66683955HCID 66683955—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthyl AcetateHCID 8857—
ProductHCID 66685270HCID 6668527029.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A tube was charged with trans-cyclohexanediamine (162 mg, 1.42 mmol, 0.5 equiv), K2CO3 (783 mg, 5.67 mmol, 2.0 equiv), 3-bromo-5-phenyl-thiophene-2-carboxylic acid methyl ester (1.01 g, 3.40 mmol, 1.2 equiv), CuI (270 mg, 1.42 mmol, 0.5 equiv), (R)-3-Cyclohexyl-5-oxo-piperazine-1-carboxylic acid tert-butyl ester (800 mg, 2.83 mmol, 1.0 equiv) and 1,4-dioxane (3.0 mL). The tube was then flushed with N2 and sealed. The reaction mixtures were heated at 110° C. for 72 hours after which it was diluted with EtOAc and filtered. The filtrate was washed with 1.0 N HCl aq. solution, brine, dried (Na2SO4) and concentrated. The residue was purified by silica gel column chromatography (EtOAc/heptane, 50%) to give product (R)-3-Cyclohexyl-4-(2-methoxycarbonyl-5-phenyl-thiophen-3-yl)-5-oxo-piperazine-1-carboxylic acid tert-butyl ester 415 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040690B2
Source datasetuspto-grants-2015_05
ORD IDord-957f1efe45d64f02bdc55d90d5c9c129
Source noteuspto-grants-2015_05