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HRID 524187作成日:2026年10月27日

Quinoline-7-carboxylic acid → 5-(3,4-Dimethoxyphenyl)-4,4-dimethyl-2-[1-(quinolin-7-ylcarbonyl)piperidin-4-yl]-2,4-dihydro-3H-pyrazol-3-one

https://huagongshe.com/reaction/524187

反応式

関与物質

役割名称HCID仕込み量
反応物Quinoline-7-carboxylic acidHCID 599475—
反応物5-(3,4-dimethoxyphenyl)-4,4-dimethyl-2-piperidin-4-yl-2,4-dihydro-3H-pyrazol-3-one hydrochlorideHCID 66616406—
生成物5-(3,4-Dimethoxyphenyl)-4,4-dimethyl-2-[1-(quinolin-7-ylcarbonyl)piperidin-4-yl]-2,4-dihydro-3H-pyrazol-3-oneHCID 46205296—

反応手順

The title compound is prepared analogously as described for GP2-WU2 using 5-(3,4-dimethoxyphenyl)-4,4-dimethyl-2-(piperidin-4-yl)-2,4-dihydro-3H-pyrazol-3-one (compound B1) and quinoline-7-carboxylic acid as starting compounds. The crude product is purified by chromatography (amino phase silica gel and DCM) and by crystallization from DCM and diethyl ether to yield the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340522B2
出典データセットuspto-grants-2016_05
ORD IDord-94ba7250da1b4dc1b313718722120abd
出典メモuspto-grants-2016_05