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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360475생성일: 2026년 10월 27일

Sodium Carbonate → tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)ethylcarbamate

https://huagongshe.com/reaction/1360475

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriphenylphosphineHCID 11776—
반응물2-Aminophenylboronic acid hydrochlorideHCID 16427090—
반응물tert-butyl 2-(4-bromo-3-cyano-1-propyl-1H-pyrazol-5-yl)ethylcarbamateHCID 66958960—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매1-PropanolHCID 1031—
생성물tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)ethylcarbamateHCID 6695884844.7%

반응 조건

온도100 °C

반응 단계

A flask containing a mixture of tert-butyl 2-(4-bromo-3-cyano-1-propyl-1H-pyrazol-5-yl)ethylcarbamate (15.8 g, 44.2 mmol), 2-aminophenylboronic acid hydrochloride (11.5 g, 66.3 mmol), triphenylphosphine (1.04 g, 3.98 mmol), palladium (II) acetate (299 mg, 1.33 mmol), 2 M aqueous sodium carbonate (67 mL, 133 mmol), 1-propanol (77.4 mL), and water (15.5 mL) was heated overnight under a nitrogen atmosphere in a 100° C. oil bath. The reaction was allowed to cool to ambient temperature and water (300 mL) was added. The mixture was extracted with chloroform, dried over magnesium sulfate, filtered, and concentrated to provide an oil that was purified twice by flash chromatography (silica gel, first column: eluted sequentially with 0-10% CMA in chloroform, and then 25% CMA in chloroform; second column: gradient elution with 50-60% ethyl acetate in hexanes) to yield 7.3 g of tert-butyl 2-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)ethylcarbamate as a yellow resin.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879849B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-55c1a403d6274c1bb32e1309d1eaa703
출처 메모uspto-grants-2011_02