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HRID 1373616作成日:2026年10月27日

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

https://huagongshe.com/reaction/1373616

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-(7-Oxo4-trifluoromethyl-5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yloxy)-butyraldehydeHCID 21073376—
生成物7-{4-[4-(5,6,7,8-Tetrahydro-naphthalen-1-yl)-piperazin-1-yl]-butoxy}-5-trifluoromethyl-3,4-dihydro-1H-[1,8]naphthyridin-2-oneHCID 21073705—

反応手順

In a manner similar to that of other examples above, 1-(5,6,7,8-tetrahydro-naphthalen-1-yl)-piperazine was coupled by reductive amination to 4-(7-oxo-4-trifluoromethyl-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: 503.1 (Exact Mass: 502.26).

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-7b3c6ee8403349ebbc719e70bc756807
出典メモuspto-grants-2007_01