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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579162Erstellt: 24. Oktober 2026

Potassium Carbonate → HCID 66685270, Verbindung

https://huagongshe.com/de/reaction/579162

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1,4-DioxaneHCID 31275—
EduktMethyl 3-bromo-5-phenyl-thiophene-2-carboxylateHCID 20775762—
EduktHCID 66683955HCID 66683955—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 66685270HCID 6668527029,4%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040690B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-957f1efe45d64f02bdc55d90d5c9c129
Quellennotizuspto-grants-2015_05