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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1783763생성일: 2026년 10월 24일

7,12-Dimethylbenz(a)anthracene → 6-(3-amino-2-fluoropropyl)-9-chloro[1,2,4]triazolo[3,4-a]isoquinolin-3(2H)-one

https://huagongshe.com/ko/reaction/1783763

반응식

참여 물질

역할이름HCID투입량
반응물7,12-Dimethylbenz(a)anthraceneHCID 6001—
반응물6-[3-(allylamino)-2-fluoropropyl]-9-chloro[1,2,4]triazolo[3,4-a]isoquinolin-3(2H)-oneHCID 57590911—
촉매HCID 178418397HCID 178418397—
용매1,2-DichloroethaneHCID 11—
생성물6-(3-amino-2-fluoropropyl)-9-chloro[1,2,4]triazolo[3,4-a]isoquinolin-3(2H)-oneHCID 57590909—

반응 조건

온도50 °C

반응 단계

6-[3-(allylamino)-2-fluoropropyl]-9-chloro[1,2,4]triazolo[3,4-a]isoquinolin-3(2H)-one (6-4)(18 mg, 0.054 mmol, 1.0 equiv) and DMBA (25.2 mg, 0.16 mmol, 3.0equiv) and tetrakis(triphenylphosphine)palladium(0) (3 mg, 2.60 μmol, 0.05 equiv) were suspended in ClCH2CH2Cl (1 mL). The resulted yellow suspension was heated at 50° C. LCMS at 5 hours showed mostly product. The crude was purified with reverse phase HPLC H2O/CH3CN gradient w/0.1% TFA present) to afford the pure product (6-5). 1H NMR (500 MHz, CD3OD) δ 8.26 (d, 1H, J=2.3 Hz), 7.88 (d, 1H, J=8.5 Hz), 7.72 (dd, 1H, J=8.5, 2.3 Hz), 7.61 (s, 1H), 5.19-4.94 (dm, 1H, J=50.0 Hz), 3.52-3.33 (m, ˜4H, overlap w/solvent peak). LRMS m/z (M+H) 295.3 found, 295.1 required.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07501435B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-2926e3e4600e447a87afe72415ea8a63
출처 메모uspto-grants-2009_03