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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434680Generated: October 30, 2026

Piperidine → HCID 20258995, compound

https://huagongshe.com/reaction/434680

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 1 N 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 numberUS04399134
Source datasetuspto-grants-1983_08
ORD IDord-fd5c2af7fb2341a8ab39a135cc7e82a3
Source noteuspto-grants-1983_08