HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116518Generated: November 5, 2026
tert-Butyl piperazine-1-carboxylate → HCID 69196157, compound
https://huagongshe.com/reaction/2116518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 69195970 | HCID 69195970 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69196157 | HCID 69196157 | 49% |
Reaction Steps
A stirred suspension of 8-chloro-3-(phenyloxy)quinoline (D7)(0.115 g, 0.45 mmol), 1,1-dimethylethyl 1-piperazinecarboxylate (0.084 g, 0.45 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.012 g, 0.014 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.016 g, 0.041 mmol) and sodium tert-butoxide (0.043 g, 0.45 mmol) in degassed toluene (2.5 ml) was heated in a sealed tube at 150° C. for 10 mins in a microwave oven. The cooled reaction mixture was washed with water (20 ml), dried (MgSO4) and concentrated in vacuo to an oil. The oil was purified by chromatography over silica gel eluting with a gradient of ethyl acetate/hexane to afford the title compound (D8) as a yellow oil (0.09 g, 0.22 mmol, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439243B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-f55fe3199b7f45b4a8a9e43263d0afa2 |
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| Source note | uspto-grants-2008_10 |
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