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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | tert-butyl N-(5-bromo-2-chlorophenyl)carbamate | HCID 57840526 | — |
| Reagent | Cesium carbonate | HCID 10796 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | Palladium (II) acetate | HCID 4144353 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl N-[2-chloro-5-(piperazin-1-yl)phenyl]carbamate | HCID 57840409 | 57.11% |
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 dataset | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-839e83634a9943b98e2511e3c8112ffb |
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| Source note | 750 AstraZeneca ELN dataset |
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