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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648Generated: October 28, 2026

tert-Butyl piperazine-1-carboxylate → HCID 178418197, compound

https://huagongshe.com/reaction/648

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4-Bromo-2-chloro-1-ethoxybenzeneHCID 21938513—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
ProductHCID 178418197HCID 1784181970%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 50 mL round-bottomed flask, PALLADIUM ACETATE (0.014 g, 0.06 mmol) was treated with BINAP (0.079 g, 0.13 mmol) under nitrogen in degassed Toluene (12.74 ml). The reaction was heated to 80 °C and was stirred for 10 min. To the flask was then added tert-butyl piperazine-1-carboxylate (0.237 g, 1.27 mmol), cesium carbonate (0.208 g, 0.64 mmol), potassium carbonate (0.176 g, 1.27 mmol), and 18-CROWN-6 (0.034 g, 0.13 mmol). The reaction was then treated with 4-bromo-2-chloro-1-ethoxybenzene (0.300 g, 1.27 mmol) and was allowed to stir at 80°C 5 h. **LCMS High pH:** No reaction observed

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-3dc45e0d006e4925b34d5e9919e16fc1
Source note750 AstraZeneca ELN dataset