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HRID 69130作成日:2026年10月25日

Diisopropylethylamine → 7-methyl-8-{[4-(pyridin-3-ylmethyl)piperazin-1-yl]carbonyl}-1-(tetrahydro-2H-pyran-4-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-one dihydrochloride

https://huagongshe.com/reaction/69130

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-[(Pyridin-3-yl)methyl]piperazineHCID 156975—
反応物Sodium BicarbonateHCID 516892—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物Hydrogen chloride-ethyl acetateHCID 21866389—
反応物7-methyl-4-oxo-1-(tetrahydro-2H-pyran-4-yl)-4,5-dihydro-1H-pyrazolo[4,3-c]quinoline-8-carboxylic acidHCID 136336854—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物7-methyl-8-{[4-(pyridin-3-ylmethyl)piperazin-1-yl]carbonyl}-1-(tetrahydro-2H-pyran-4-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-one dihydrochlorideHCID 136336858—

反応手順

To a mixture of 120 mg of 7-methyl-4-oxo-1-(tetrahydro-2H-pyran-4-yl)-4,5-dihydro-1H-pyrazolo[4,3-c]quinoline-8-carboxylic acid and 2.4 mL of DMF were added 130 mg of 1-(pyridin-3-ylmethyl)piperazine, 0.19 mL of DIPEA, and 177 mg of TBTU, followed by stirring at room temperature overnight. The reaction mixture was ice-cooled and poured into a saturated aqueous sodium hydrogen carbonate solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform/methanol=100/0-92/8) to obtain white powder. The powder was suspended in 1 mL of methanol, and 0.37 mL of a 4 M hydrogen chloride-ethyl acetate solution was added thereto, followed by stirring for 30 minutes. The obtained powder was collected by filtration, washed with methanol, and then dried under reduced pressure to obtain 82 mg of 7-methyl-8-{[4-(pyridin-3-ylmethyl)piperazin-1-yl]carbonyl}-1-(tetrahydro-2H-pyran-4-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-one dihydrochloride as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822448B2
出典データセットuspto-grants-2014_09
ORD IDord-eed1a08719ed4f208c9b20c0edd39357
出典メモuspto-grants-2014_09