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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635Generated: October 23, 2026

Piperazine → tert-butyl N-[2-chloro-5-(piperazin-1-yl)phenyl]carbamate

https://huagongshe.com/en/reaction/635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactanttert-butyl N-(5-bromo-2-chlorophenyl)carbamateHCID 57840526—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
Producttert-butyl N-[2-chloro-5-(piperazin-1-yl)phenyl]carbamateHCID 5784040957.11%

Reaction Conditions

Temperature110 °C

Reaction Steps

palladium(II) acetate (0.110 g, 0.49 mmol), BINAP (0.244 g, 0.39 mmol) and CS2CO3 (1.594 g, 4.89 mmol) were added to a mixture of [Reactants] and piperazine (2.76 g, 32.10 mmol) in toluene (10 mL), The suspension were heated to 110 °C for 16 hours, LCMS showed product mass [M+1]:312.0 at retention time RT=1.69 min (polar short purity method). Workup reaction by additional of water (10mL), extracted with EtOAc (3x20 mL), washed with brine, dried with Na2SO4, evaporated off solvent to give a residue, which was purified by isco chromatographer, eluting with 0-10% MeOH in DCM to give as a yellow solid. LCMS confirmed the target compound.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-839e83634a9943b98e2511e3c8112ffb
Source note750 AstraZeneca ELN dataset