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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1381557생성일: 2026년 10월 27일

6-Chloroindoline-2,3-dione → 5-Amino-6-chloroindole-3-acetonitrile

https://huagongshe.com/reaction/1381557

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloroindoline-2,3-dioneHCID 241331—
반응물6-chloro-5-nitro-1H-indoleHCID 18932857—
반응물6-Chloro-5-nitroindole-3-acetonitrileHCID 21276200—
반응물6-Chloro-5-nitroisatinHCID 23354431—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물5-Amino-6-chloroindole-3-acetonitrileHCID 21276186—

반응 단계

This intermediate was prepared by the sequence 6-chloroisatin, 6-chloro-5-nitroisatin, 6-chloro-5-nitroindole, 6-chloro-5-nitrogramine and 6-chloro-5-nitroindole-3-acetonitrile which was hydrogenated with 10% Pd/C until 3 equiv. of hydrogen were taken up. The catalyst was removed by filtration and the residue concentrated in vacuo to give a dark brown solid. Trituration with cold EtOH gave desired pure product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04803218
출처 데이터셋uspto-grants-1989_02
ORD IDord-0a418df9f188460d8a5d72c1cd6bec41
출처 메모uspto-grants-1989_02