돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411770생성일: 2026년 10월 26일

Benzene → But-2-enedioic Acid Mono-[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/411770

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물Fumaryl chlorideHCID 5325504—
반응물1-hydroxymethyl-3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-pyrrole-2,5-dioneHCID 9867338—
용매AcetoneHCID 180—
용매DichloromethaneHCID 6344—
생성물But-2-enedioic Acid Mono-[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 6994508660%

반응 단계

To a solution of 1-Hydroxymethyl-3-(1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-pyrrole-2,5-dione, prepared as in example 1a, in 1:4 CH2Cl2:benzene, were added a large excess of fumaryl chloride and excess diisopropylethylamine. The reaction was stirred at room temperature for 20 min. Acetone and water were, added. The reaction mixture was diluted with CH2Cl2, washed with water, cold saturated NaHCO3, water and dried over Na2SO4. The resulting but-2-enedioic acid mono-[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 was purified by flash chromatography (yield 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559164B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-73a3beae291a44caba9931cc95d6bb7f
출처 메모uspto-grants-2003_05