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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360561생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-aminobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 66958656—
촉매Adams' catalystHCID 345198—
용매Trifluoroacetic acidHCID 6422—
생성물1-(4-aminobutyl)-2-ethyl-6,7,8,9-tetrahydro-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 66959128—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879849B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-b7a4ee3ce7ea4fdc819923ddb491c211
출처 메모uspto-grants-2011_02