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HRID 1373646作成日:2026年10月25日

1-methyl-8-piperazin-1-yl-3,4-dihydro-1H-quinolin-2-one hydrochloride → 7-{4-[4-(1-Methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-8-yl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-one

https://huagongshe.com/reaction/1373646

反応式

関与物質

役割名称HCID仕込み量
反応物1-methyl-8-piperazin-1-yl-3,4-dihydro-1H-quinolin-2-one hydrochlorideHCID 21073199—
反応物4-((7-Oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)oxy)butanalHCID 21073377—
生成物7-{4-[4-(1-Methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-8-yl)-piperazin-1-yl]-butoxy}-3,4-dihydro-1H-[1,8]naphthyridin-2-oneHCID 21073496—

反応手順

In a manner similar to that of other examples above, 1-methyl-8-piperazin-1-yl-3,4-dihydro-1H-quinolin-2-one hydrochloride 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. MS: APCI: M+1: 464.6 (Exact Mass: 463.26).

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-0bc9d3d5ab284f18abf4848f41bc88ec
出典メモuspto-grants-2007_01