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HRID 1360561作成日:2026年10月27日

1-(4-aminobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinolin-4-amine → 1-(4-aminobutyl)-2-ethyl-6,7,8,9-tetrahydro-2H-pyrazolo[3,4-c]quinolin-4-amine

https://huagongshe.com/reaction/1360561

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-aminobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 66958656—
触媒Adams' catalystHCID 345198—
溶媒Trifluoroacetic acidHCID 6422—
生成物1-(4-aminobutyl)-2-ethyl-6,7,8,9-tetrahydro-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 66959128—

反応手順

Platinum (IV) oxide (4 g) was added to a solution of 1-(4-aminobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinolin-4-amine (approximately 24 mmol, prepared as described in Part A of Examples 349-453) in trifluoroacetic acid (80 mL), and the mixture was shaken under hydrogen pressure (50 psi, 3.4×105 Pa) for two days and subsequently filtered through a layer of CELITE filter agent. The filter cake was washed with methanol, and the filtrate was concentrated under reduced pressure. Water (10 mL) was added, and the resulting solution was adjusted to pH 14 with the addition of 50% aqueous sodium hydroxide. The resulting mixture was extracted with dichloromethane, and the extracts were dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 1-(4-aminobutyl)-2-ethyl-6,7,8,9-tetrahydro-2H-pyrazolo[3,4-c]quinolin-4-amine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07879849B2
出典データセットuspto-grants-2011_02
ORD IDord-b7a4ee3ce7ea4fdc819923ddb491c211
出典メモuspto-grants-2011_02