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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346711생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → 2-(4-(4,9-diethoxy-1-oxo-1H-benzo[f]isoindol-2(3H)-yl)phenyl)-N-((4-fluorophenyl)sulfonyl)acetamide

https://huagongshe.com/reaction/346711

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물DiisopropylethylamineHCID 81531—
반응물4-FluorobenzenesulfonamideHCID 120231—
반응물[4-(4,9-diethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acidHCID 9931112—
용매DichloromethaneHCID 6344—
생성물2-(4-(4,9-diethoxy-1-oxo-1H-benzo[f]isoindol-2(3H)-yl)phenyl)-N-((4-fluorophenyl)sulfonyl)acetamideHCID 989408235.3%

반응 단계

To a solution of carbonyldiimidazole (13.2 mg, 0.081 mmol) and [4-(4,9-diethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid (30 mg, 0.074 mmol) in dichloromethane (2 ml) was added 4-fluorobenzenesulphonamide (14.3 mg, 0.081 mmol) and N,N-diisopropylethylamine (10.5 mg, 0.81 mmol). The mixture was stirred at ambient temperature under an atmosphere of nitrogen overnight. The reaction mixture was diluted with dichloromethane (3 ml) and then washed with 2N hydrochloric acid (5 ml). The organic phase was dried (MgSO4) and then concentrated in vacuo to give a brown gum. The residue was purified using mass directed autopurification to give the title compound as a white solid (14.7 mg, 35.3%). MH+563.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173047B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-74fcd33b573a41169ca8bf9fead8c9a7
출처 메모uspto-grants-2007_02