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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 717Erstellt: 23. Oktober 2026

Benzene, 4-bromo-1,2-dimethoxy- → tert-butyl (2R)-4-(3,4-dimethoxyphenyl)-2-propan-2-ylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/717

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 4-bromo-1,2-dimethoxy-HCID 76114—
Edukt(R)-1-Boc-2-isopropylpiperazineHCID 24820392—
ReagenzPotassium tert-butoxideHCID 23665647—
KatalysatorTris(1,1-dimethylethyl)phosphineHCID 83681—
KatalysatorBis(tri-tert-butylphosphine)palladium(0)HCID 2734558—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl (2R)-4-(3,4-dimethoxyphenyl)-2-propan-2-ylpiperazine-1-carboxylateHCID 6909881290,52%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

22-Apr-09 09:56:23 +0100 4-bromo-1,2-dimethoxybenzene (0.068 mL, 0.46 mmol), (R)-tert-butyl 2-isopropylpiperazine-1-carboxylate (126 mg, 0.55 mmol) and BIS(TRI-T- BUTYLPHOSPHINE)PALLADIUM(0) (23.54 mg, 0.05 mmol) and potassium 2-methylpropan-2-olate (76 mg, 0.64 mmol) were suspended in THF (5 mL) and sealed into a microwave tube. The reaction was heated to 150 °C for 10 minutes in the microwave reactor and cooled to RT. LC-MS shows no starting material. The reaction mixture was filtered and the crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford (R)-tert-butyl 4-(3,4-dimethoxyphenyl)-2-isopropylpiperazine-1-carboxylate (152 mg, 91 %) as a yellow gum.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-dcac8bcfa5124a8baee8e28e5e992678
Quellennotiz750 AstraZeneca ELN dataset