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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 914666생성일: 2026년 10월 25일

5-fluoro-1H-indole-3-carbaldehyde → 2-[4-(5-fluoro-1H-indol-3-ylmethylene)-5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl]-N-isopropyl-N-(6-methoxy-pyridin-3-yl)-acetamide

https://huagongshe.com/reaction/914666

반응식

참여 물질

역할이름HCID투입량
반응물5-fluoro-1H-indole-3-carbaldehydeHCID 259089—
반응물N-isopropyl-N-(6-methoxy-pyridin-3-yl)-2-(5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl)-acetamideHCID 58957931—
생성물2-[4-(5-fluoro-1H-indol-3-ylmethylene)-5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl]-N-isopropyl-N-(6-methoxy-pyridin-3-yl)-acetamideHCID 13635244465.4%

반응 단계

Following the procedure described for Example 1 (A), Step A, N-isopropyl-N-(6-methoxy-pyridin-3-yl)-2-(5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl)-acetamide (Preparation 11) (120 mg, 0.207 mmol) was condensed with 5-fluoro-1H-indole-3-carbaldehyde (48 mg, 0.248 mmol). Purification by medium pressure chromatography eluting with a solvent gradient (1% MeOH in CH2Cl2 to 7% MeOH in CH2Cl2) yielded 85 mg of 2-[4-(5-fluoro-1H-indol-3-ylmethylene)-5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl]-N-isopropyl-N-(6-methoxy-pyridin-3-yl)-acetamide. MS 628.8 (M+1), 626.4 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265104B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-169c57aba5ce41cf97b8a6df33af4a26
출처 메모uspto-grants-2007_09