HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465733Generated: October 30, 2026
Cesium carbonate → tert-Butyl 4-(6-cyanoquinolin-2-yl)-3-oxopiperazine-1-carboxylate
https://huagongshe.com/reaction/1465733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Reactant | 2-Chloroquinoline-6-carbonitrile | HCID 11252468 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | tert-Butyl 4-(6-cyanoquinolin-2-yl)-3-oxopiperazine-1-carboxylate | HCID 131732662 | — |
Reaction Steps
To a 25 mL flask was added a stir bar, 2-chloroquinoline-6-carbonitrile (0.015 g, 0.79 mmol), Pd2 dba3 (0.072 g, 0.08 mmol), Xantphos (0.09 g, 0.16 mmol), cesium carbonate (0.36 g, 1.13 mmol) and tert-Butyl 3-oxopiperazine-1-carboxylate (0.31 g, 1.6 mmol). The resulting mixture was degassed and purged with N2 (3×). To the flask was added 1,4-dioxane (10 mL). The reaction mixture was then refluxed at 100° C. overnight. Analysis of the reaction mixture by LC indicated that reaction had gone to completion. The solution was concentrated in vacuo and the resulting crude was dissolved in EtOAc and washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified by silica gel column chromatography (10% MeOH in DCM) to provide the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999991B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-39f5ec5f0ff042449979f97d353b15d4 |
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| Source note | uspto-grants-2015_04 |
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