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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2081700생성일: 2026년 10월 26일

N-[1-(3-nitrobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamide → N-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamide

https://huagongshe.com/reaction/2081700

반응식

참여 물질

역할이름HCID투입량
반응물N-[1-(3-nitrobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamideHCID 19780401—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물N-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamideHCID 19780416—

반응 단계

The nitrobenzylindole (Example 3) (2.7 g) was dissolved in methanol (125 ml) and ethyl acetate (125 ml), and 10% palladium on charcoal (0.5 g) added. The reaction mixture was hydrogenated in a Parr bottle at 50 p.s.i. with shaking until hydrogen uptake was complete (approximately 1 hour). The catalyst was filtered off through Celite and the solvent removed in vacuo to give N-[1-(3-aminobenzyl)indol-5-ylcarbonyl]-2-methylbenzene sulphonamide as a foam. This crude product was used in the next step without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05185361
출처 데이터셋uspto-grants-1993_02
ORD IDord-845656225af949548418a55035863d1e
출처 메모uspto-grants-1993_02