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HRID 1373612作成日:2026年10月27日

1-(5,6,7,8-Tetrahydronaphthalen-1-yl)piperazine → 5-Methyl-7-{4-[4-(5,6,7,8-tetrahydro-naphthalen-1-yl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-one

https://huagongshe.com/reaction/1373612

反応式

関与物質

役割名称HCID仕込み量
反応物1-(5,6,7,8-Tetrahydronaphthalen-1-yl)piperazineHCID 98698—
反応物4-(4-Methyl-7-oxo-5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yloxy)-butyraldehydeHCID 21073350—
生成物5-Methyl-7-{4-[4-(5,6,7,8-tetrahydro-naphthalen-1-yl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-oneHCID 21073421—

反応手順

The title compound was prepared by reductive amination of 4-(4-methyl-7-oxo-5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yloxy)-butyraldehyde with 1-(5,6,7,8-tetrahydro-naphthalen-1-yl)-piperazine according to the above procedure. MS: APCI: M+1: 450.0 (Exact Mass: 448.28).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07160888B2
出典データセットuspto-grants-2007_01
ORD IDord-a05f6472d8fa4baeab359f3e06a2916c
出典メモuspto-grants-2007_01