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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 511Erstellt: 23. Oktober 2026

3-Bromopyridine → tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromopyridineHCID 12286—
Edukt(R)-1-Boc-3-methylpiperazineHCID 2756811—
ReagenzCesium carbonateHCID 10796—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkttert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylateHCID 895559810%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

diacetoxypalladium (9.34 mg, 0.04 mmol) and RuPhos (0.039 g, 0.08 mmol) were suspended in 1,4 dioxane (5 mL), degassed and stirred at 50 °C for 10 minutes. Then (R)-tert-butyl 3-methylpiperazine-1-carboxylate (0.100 g, 0.50 mmol), 3-bromopyridine (0.040 mL, 0.42 mmol) and cesium carbonate (0.203 g, 0.62 mmol) were added and the reaction mixture was stirred at 100 °C for 16 h. LCMS showed only 5% conversion to desired product. This was part of a screen and Ruphos, sodium tert-butoxide in toluene gave far better conversion so this was abandoned.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-a21d6ec12c02473a98dce7de6b637849
Quellennotiz750 AstraZeneca ELN dataset