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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434683Generated: October 30, 2026

4-Benzylpiperidine → HCID 13044290, compound

https://huagongshe.com/reaction/434683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzylpiperidineHCID 31738—
ReactantHCID 13472993HCID 13472993—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 13044290HCID 1304429014.1%

Reaction Steps

In a 50 ml flask were placed 2.5 g of 9-fluoro-8-bromo-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid, 6.4 g of 4-benzylpiperidine and 25 ml of hexamethylphosphoric triamide and the mixture was stirred at 160° C. in an argon gas atmosphere for 7 hours. After disappearance of the starting materials was confirmed by thin layer chromatography, hexamethylphosphoric triamide was removed using a vacuum pump followed by cooling to room temperature. To the residue was added ethyl acetate and then several drops of concentrated hydrochloric acid and the mixture was allowed to stand in a refrigerator for 1 day. The crystals which formed were collected by filtration and recrystallized from dimethylformamide to give 0.45 g of 9-fluoro-8-(4-benzyl-1-piperidyl)-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid. m.p. 230°-232° C., white rhombic crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399134
Source datasetuspto-grants-1983_08
ORD IDord-6ffc7e04be61457cb4a266f4be85b3d8
Source noteuspto-grants-1983_08