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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783627Generated: November 1, 2026

Piperidine → HCID 178467445, compound

https://huagongshe.com/reaction/1783627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-Ethoxy-quinazoline-6-carbaldehydeHCID 57590624—
ReactantHCID 178516943HCID 178516943—
SolventEthanolHCID 702—
ProductHCID 178467445HCID 17846744530%

Reaction Steps

The mixture of 4-ethoxy-quinazoline-6-carbaldehyde (example 10b, 20 mg, 0.1 mmol,), 2-[2-(3-Fluoro-phenyl)-ethylamino]-thiazol-4-one (example 10c, 24 mg, 0.1 mmol) and piperidine (10 ul, 0.1 mmol) in anhydrous ethyl alcohol (1 ml) was microwaved at 160° C. for 25 min. After cooling the reaction to room temperature, the solid was collected by filtration, then washed with MeOH and dried to afford 5-[1-(4-ethoxy-quinazolin-6-yl)-meth-(Z)-ylidene]-2-[2-(3-fluoro-phenyl)-ethylamino]-thiazol-4-one (12 mg, 30%) as light yellow solid. LC-MS m/e 423 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501428B2
Source datasetuspto-grants-2009_03
ORD IDord-ac6f378a36264ca09a05c3888f6890ed
Source noteuspto-grants-2009_03