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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373534Generated: October 25, 2026

1-(2-Chloro-6-piperazin-1-yl-phenyl)-ethanone → 7-{4-[4-(2-Acetyl-3-chloro-phenyl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-one

https://huagongshe.com/reaction/1373534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloro-6-piperazin-1-yl-phenyl)-ethanoneHCID 21073144—
Reactant4-((7-Oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)oxy)butanalHCID 21073377—
Product7-{4-[4-(2-Acetyl-3-chloro-phenyl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-oneHCID 21073567—

Reaction Steps

In a manner similar to that of other examples, above, 1-(2-chloro-6-piperazin-1-yl-phenyl)-ethanone was coupled by reductive amination to 4-(7-oxo-5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yloxy)-butyraldehyde followed by typical workup and purification to give the title compound, mp 115° C. MS: APCI: M+1: 457.2 (Exact Mass: 456.19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160888B2
Source datasetuspto-grants-2007_01
ORD IDord-765352bbd4204a32ab706ff8422bd5c0
Source noteuspto-grants-2007_01