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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24486생성일: 2026년 10월 24일

Piperidine → 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide

https://huagongshe.com/ko/reaction/24486

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Indole-2-carboxaldehydeHCID 96389—
반응물2-Oxoindoline-5-sulfonamideHCID 10198232—
용매EthanolHCID 702—
생성물3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amideHCID 5423212883%

반응 단계

A mixture of 5-aminosulfonyl-2-oxindole (106 mg), indole-2-carbaldehyde (87 mg) (prepared according to Synthetic Communications, 1993, 23, 3109) and piperidine (4 mg) in ethanol (2 mL) was held in a sealed tube at 90° C. for 3 hours. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in a vacuum oven to give 140 mg (83% yield) of 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-e5497abd8c934133ad7a0fe805074e9e
출처 메모uspto-grants-2005_02