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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916262Generated: October 26, 2026

Piperidine → HCID 178518096, compound

https://huagongshe.com/reaction/916262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1,5-Naphthyridine-2-carbaldehydeHCID 11586336—
ReactantHCID 178516792HCID 178516792—
SolventIsopropanolHCID 3776—
ProductHCID 178518096HCID 178518096—

Reaction Steps

To a mixture of 2-(2-chloro-4-fluoro-benzylamino)-4-oxo-4,5-dihydro-imidazole-1-carboxylic acid benzyl ester (70.1 mg, 0.19 mmol), 1,5-naphthyridine-6-carboxaldehyde (28.7 mg, 0.18 mmol) and iPrOH (5.0 mL) in a 25-mL round bottom flask was added piperidine (0.05 mL) and the suspension was then heated under refluxing for 4 hrs to give a suspension. The reaction mixture was cooled to r.t. and the solid was collected by filtration, washed with MeOH, and ether to give 2-(2-chloro-4-fluoro-benzylamino)-5-[1,5]naphthyridin-2-ylmethylene-1,5-dihydro-imidazol-4-one as a light yellow solid, 30.6 mg (43.0%). HR-ES (+) m/e calcd. for C19H13FClN5O: (M+H)+ 382.0866. Found: 382.0866.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268231B2
Source datasetuspto-grants-2007_09
ORD IDord-5c0b90b89e014741ade219b7a92f58bc
Source noteuspto-grants-2007_09