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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583611Generated: November 3, 2026

Piperidine → HCID 20258995, compound

https://huagongshe.com/reaction/1583611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 20258998HCID 20258998—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 20258995HCID 2025899548.6%

Reaction Steps

Anhydrous piperidine (8 g) was added to 5.3 g of 8-chloro-9-fluoro-5-methyl-2-acetyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine. 70 ml of hexamethylphosphoric triamide was added thereto and the mixture was allowed to react at 140° C. on an oil bath for 6 hours. After completion of the reaction any excess solvent and piperidine were removed by distillation under reduced pressure and 100 ml of ethyl acetate was added to the residue to precipitate light yellow crystals. The crystals thus obtained were separated by filtration and 300 ml of water was added thereto followed by adjusting the resulting solution to a pH of 2 with 1N hydrochloric acid. The solution was heated and filtered. The filtrate was concentrated to 50 ml and rendered alkaline with a 10% aqueous sodium hydroxide solution to obtain 3.0 g of 8-(1-piperidyl)-9-fluoro-5-methyl-2-acetyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552879
Source datasetuspto-grants-1985_11
ORD IDord-92a35f24f62040b492780a96e9bca7be
Source noteuspto-grants-1985_11