HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358050Generated: October 26, 2026
1-Acetylpiperazine → HCID 18186383, compound
https://huagongshe.com/reaction/1358050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 18186409 | HCID 18186409 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Dibenzalacetone palladium | HCID 72499888 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18186383 | HCID 18186383 | 41.1% |
Reaction Steps
A mixture of 1-(4-bromobenzyl)-6-phenylmethoxy-2-(4-fluorophenyl)-1,2,3,4-tetrahydroisoquinoline (1.0 g, 1.99 mmol), dibenzylideneacetone palladium (36 mg, 0.04 mmol), BINAP (74 mg, 0.12 mmol), sodium tert-butoxide (0.29 g, 3.0 mmol) and N-acetylpiperazine (0.38 g, 3.0 mmol) in 2 ml of toluene were added to a sealed tube under an argon atmosphere and heated at 80° C. for 16 h. The sealed tube was cooled to room temperature and the contents of the tube transferred to a separatory funnel. Ethyl acetate and water were added and the organic layer was separated. The combined organic layers were dried over MgSO4, concentrated, and purified by column chromatography (SiO2, chloroform/methanol, 99:1) to provide the title compound (0.45 g, 41% yield): ES-MS (m/z) 550 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06593322B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-34f61fe4560b42608aec614caedc713a |
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| Source note | uspto-grants-2003_07 |
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