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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411779생성일: 2026년 10월 24일

N,N-Diethylethylenediamine → 3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-pyrrole-1-carboxylic acid (2-diethylamino-ethyl)-amide

https://huagongshe.com/ko/reaction/411779

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylethylenediamineHCID 60993—
반응물Bis(4-nitrophenyl) carbonateHCID 78756—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물1H-pyrrole-2,5-dione, 3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-HCID 5327686—
용매TetrahydrofuranHCID 8028—
생성물3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-pyrrole-1-carboxylic acid (2-diethylamino-ethyl)-amideHCID 985032010.3%

반응 단계

To a cold solution of 3-(1-Methyl-3-indolyl)-4-(1-methyl-6-nitro-3-indolyl)-1H-pyrrole-2,5-dione (200 mg, 0.5 mmol) (see Davis U.S. Pat. No. 5,057,614) in THF (7 mL) was added dropwise, lithium bis(trimethylsilyl)amide (0.55 mmol, 0.55 mL, 1 M in THF). The resulting red suspension was stirred for 15 min. Bis(p-nitrophenyl)carbonate (213 mg, 0.7 mmol) was added. The solution was stirred at 0° C. for 0.5 h. Diethylaminoethylamine (69.7 mg, 0.6 mmol) in THF (2 mL) was added, and stirring was continued for 2 h. The solvent was evaporated and the residue was purified by flash chromatography to give 3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-pyrrole-1-carboxylic acid (2-diethylamino-ethyl)-amide (28 mg, 10%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559164B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-d53d946c859d400989ebf0858bba6426
출처 메모uspto-grants-2003_05