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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521073생성일: 2026년 10월 24일

2-Oxo-1,3-dihydroindole-6-carboxylic acid → 6-(cis-2,3,4a,5,6,10b-Hexahydro-1H-benzo[f]quinoline-4-carbonyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/521073

반응식

참여 물질

역할이름HCID투입량
반응물2-Oxo-1,3-dihydroindole-6-carboxylic acidHCID 7213323—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물(4aS,10bR)-1,2,3,4,4a,5,6,10b-Octahydrobenzo[f]quinolineHCID 12327022—
생성물6-(cis-2,3,4a,5,6,10b-Hexahydro-1H-benzo[f]quinoline-4-carbonyl)-1,3-dihydro-indol-2-oneHCID 8665411612%

반응 단계

The title compound is prepared from 2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid and cis-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexa-fluorophosphate is used]. Yield: 12% of theory; LC (method 4): tR=1.90 min; Mass spectrum (ESI+): m/z=347 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328072B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-4444cd1e5ecc472381c39bb7120c7cbe
출처 메모uspto-grants-2016_05