HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242010Generated: October 30, 2026
1,4-Dioxa-8-azaspiro(4.5)decane → 1-(5-Fluoroquinolin-8-yl)piperidin-4-one
https://huagongshe.com/reaction/2242010
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxa-8-azaspiro(4.5)decane | HCID 67435 | — |
| Reactant | 8-Bromo-5-fluoroquinoline | HCID 14548347 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Fluoroquinolin-8-yl)piperidin-4-one | HCID 59204848 | — |
Reaction Steps
To a 2-L reactor with a stirrer, a thermocouple, a condenser and nitrogen inlet were charged 8-bromo-5fluoroquinoline (50 g), tetrahydrofuran (795 g), Pd2(dba)3 (3.78 g), Cymap (1.6 g), and 1,4-Dioxa-8-azaspiro[4.5]decane (47.3 g). the mixture was heated to reflux (66° C.) and the reaction was complete. The reaction mixture was quenched into a 5 L reactor containing 1000 g of water and 640 g of MTBE. The bottom aqueous layer was split off and the organic layer was washed with 5% NaOH (1120 g) and 20% NaCl (2×100 g). The solvent was evaporated, weight 87 g vs 79.4 g by theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07671056B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-0d460ed6d61c44a69675e58821272a43 |
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| Source note | uspto-grants-2010_03 |
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