돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24481생성일: 2026년 10월 24일

Piperidine → HCID 53888754, 화합물

https://huagongshe.com/ko/reaction/24481

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
반응물2-Oxo-2,3-dihydro-1H-indole-5-sulfonic acid dimethylamideHCID 9816185—
용매EthanolHCID 702—
생성물HCID 53888754HCID 5388875457%

반응 단계

A mixture of 5-dimethylaminosulfonyl-2-oxindole (96 mg), 3-methylindole-2-carbaldehyde (56 mg) (prepared according to Synthetic Communications, 1986, 16, 1799) and piperidine (30 mg) in ethanol (1 mL) was held in a sealed tube at 90° C. overnight. 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 76 mg (57% yield) of 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid dimethylamide (mixture of isomers).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-c2dc38cd3e5f41908283bfed9b702586
출처 메모uspto-grants-2005_02