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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563Erstellt: 25. Oktober 2026

tert-Butyl piperazine-1-carboxylate → tert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt7-BromoindoleHCID 2757020—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
LösungsmittelTolueneHCID 1140—
Produkttert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylateHCID 210709510%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

2-Dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl (75 mg, 0.16 mmol) and palladium (II) acetate (18.08 mg, 0.08 mmol) were dissoved in toluene (2 mL) at ambient temperature. The mixture was degassed and purged with nitrogen and warmed to 50°C for 20 mins. In a separate vessel, were mixed tert-butyl piperazine-1-carboxylate (300 mg, 1.61 mmol), 7-bromo-1H-indole (316 mg, 1.61 mmol) and sodium-t-butoxide (296 mL, 2.42 mmol) in toluene (3 mL). The mixture was degasssed and purged with nitrogen and warmed to 50°C. The catalyst solution was added to the reaction vessel and the resulting mixture was degassed and purged with nitrogen and heated at 100°C for overnight. UPLC analysis showed virtually no reaction (only 7% conversion to product). Reaction abandoned.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-b6527d32ba054a8395bc5ea7808e53a8
Quellennotiz750 AstraZeneca ELN dataset