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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583614Generated: November 2, 2026

4-Benzylpiperidine → HCID 13044290, compound

https://huagongshe.com/reaction/1583614

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 numberUS04552879
Source datasetuspto-grants-1985_11
ORD IDord-11e501964b3340779996a8de434d2c36
Source noteuspto-grants-1985_11