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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411776생성일: 2026년 10월 26일

N,N-Diethylethylenediamine → (2-dimethylamino-ethyl)-carbamic acid 3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-pyrrol-1-ylmethyl ester

https://huagongshe.com/reaction/411776

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylethylenediamineHCID 60993—
반응물Bis(4-nitrophenyl) carbonateHCID 78756—
반응물1-hydroxymethyl-3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-pyrrole-2,5-dioneHCID 9867338—
용매TetrahydrofuranHCID 8028—
생성물(2-dimethylamino-ethyl)-carbamic acid 3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-pyrrol-1-ylmethyl esterHCID 989361548.4%

반응 조건

온도0 °C

반응 단계

1-Hydroxymethyl-3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-pyrrole-2,5-dione (200 mg, 0.47 mmol), prepared as in example 1a, was dissolved in THF (10 mL). The resulting red solution was cooled in an ice bath. Lithium bis(trimethylsiliyl)amide (0.56 mL, 0.56 mmol, 1 M in THF) was added dropwise to the solution to give a red suspension. After 10 min, bis(p-nitrophenyl)carbonate (200 mg, 0.66 mmol) was added. The resulting solution was stirred at 0° C. for 20 min. Diethylaminoethylamine (90 mg, 0.78 mmol) in THF (2 mL) was added. Stirring was continued for 2 hrs. The mixture was evaporated and the residue was purified by flash chromatography to give (2-dimethylamino-ethyl)-carbamic acid 3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-pyrrol-1-ylmethyl ester (124 mg 46%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559164B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-1d1ee7fff9e34af1a5d27df8ceb736b7
출처 메모uspto-grants-2003_05