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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383707생성일: 2026년 10월 26일

2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl → N-(2,4-dimethyl-6-(6-(trifluoromethyl)-3,4-dihydroisoquinolin-2(1H)-yl)pyridin-3-yl)-3,3-dimethylbutanamide

https://huagongshe.com/reaction/383707

반응식

참여 물질

역할이름HCID투입량
반응물2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
반응물6-(Trifluoromethyl)-1,2,3,4-tetrahydroisoquinolineHCID 18176519—
반응물Potassium tert-butoxideHCID 23665647—
반응물N-(6-bromo-2,4-dimethylpyridin-3-yl)-3,3-dimethylbutanamideHCID 59868778—
용매TolueneHCID 1140—
생성물N-(2,4-dimethyl-6-(6-(trifluoromethyl)-3,4-dihydroisoquinolin-2(1H)-yl)pyridin-3-yl)-3,3-dimethylbutanamideHCID 5986872363%

반응 조건

온도100 °C

반응 단계

In a tube, a mixture of 1d (0.374 g, 1.25 mmol), 6-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline (0.301 g, 1.5 mmol) in toluene (15 ml) was degassed by nitrogen flow for 15 minutes. To this mixture was added tris(dichlorobenzylidenacetone)palladium (0) (0.037 g, 0.04 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.06 g, 0.15 mmol) and potassium tert-butoxide (0.336 g, 3.0 mmol). The tube was heated under microwave irradiation (Biotage Initiator®) for 6 hour at 100° C. The reaction mixture was cooled to room temperature, washed with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, concentrated and chromatographed to yield the title compound (0.326 g, 0.78 mmol, 63%). 1H NMR (CDCl3, 400 MHz) δ 1.14 (s, 9H), 2.19 (s, 3H), 2.27 (s, 2H), 2.35 (s, 3H), 2.91 (t, J=6.2 Hz, 2H), 3.82 (t, J=6.2 Hz, 2H), 4.62 (s, 2H), 6.39 (s, 1H), 6.55 (bs, 1H), 6.98 (d, J=7.2 Hz, 2H), 7.24 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367684B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-358469cc890e4cfb9e72d4c27b394a3e
출처 메모uspto-grants-2013_02